gsMap 1.72.3__py3-none-any.whl → 1.73.1__py3-none-any.whl

gsMap/generate_ldscore.py

@@ -1,3 +1,11 @@
+"""
+Module for generating LD scores for each spot in spatial transcriptomics data.
+
+This module is responsible for assigning gene specificity scores to SNPs
+and computing stratified LD scores that will be used for spatial LDSC analysis.
+"""
+
+import gc
 import logging
 import warnings
 from pathlib import Path
@@ -10,113 +18,205 @@ from scipy.sparse import csr_matrix
 from tqdm import trange
 
 from gsMap.config import GenerateLDScoreConfig
-from gsMap.utils.generate_r2_matrix import ID_List_Factory, PlinkBEDFileWithR2Cache, getBlockLefts
+from gsMap.utils.generate_r2_matrix import getBlockLefts, load_bfile
 
-warnings.filterwarnings("ignore", category=FutureWarning)
+# Configure warning behavior more precisely
+warnings.filterwarnings("ignore", category=FutureWarning, module="pandas")
 logger = logging.getLogger(__name__)
 
 
-# %%
-# load gtf
-def load_gtf(gtf_file, mk_score, window_size):
+def load_gtf(
+    gtf_file: str, mk_score: pd.DataFrame, window_size: int
+) -> tuple[pr.PyRanges, pd.DataFrame]:
     """
-    Load the gene annotation file (gtf).
+    Load and process the gene annotation file (GTF).
+
+    Parameters
+    ----------
+    gtf_file : str
+        Path to the GTF file
+    mk_score : pd.DataFrame
+        DataFrame containing marker scores
+    window_size : int
+        Window size around gene bodies in base pairs
+
+    Returns
+    -------
+    tuple
+        A tuple containing (gtf_pr, mk_score) where:
+        - gtf_pr is a PyRanges object with gene coordinates
+        - mk_score is the filtered marker score DataFrame
     """
-    print("Loading gtf data")
-    #
+    logger.info("Loading GTF data from %s", gtf_file)
+
     # Load GTF file
-    gtf = pr.read_gtf(
-        gtf_file,
-    )
+    gtf = pr.read_gtf(gtf_file)
     gtf = gtf.df
-    #
-    # Select the common genes
+
+    # Filter for gene features
     gtf = gtf[gtf["Feature"] == "gene"]
+
+    # Find common genes between GTF and marker scores
     common_gene = np.intersect1d(mk_score.index, gtf.gene_name)
-    #
+    logger.info(f"Found {len(common_gene)} common genes between GTF and marker scores")
+
+    # Filter GTF and marker scores to common genes
     gtf = gtf[gtf.gene_name.isin(common_gene)]
     mk_score = mk_score[mk_score.index.isin(common_gene)]
-    #
-    # Remove duplicated lines
+
+    # Remove duplicated gene entries
     gtf = gtf.drop_duplicates(subset="gene_name", keep="first")
-    #
-    # Process the GTF (open 100-KB window: Tss - Ted)
+
+    # Process the GTF (open window around gene coordinates)
     gtf_bed = gtf[["Chromosome", "Start", "End", "gene_name", "Strand"]].copy()
     gtf_bed.loc[:, "TSS"] = gtf_bed["Start"]
     gtf_bed.loc[:, "TED"] = gtf_bed["End"]
 
+    # Create windows around genes
     gtf_bed.loc[:, "Start"] = gtf_bed["TSS"] - window_size
     gtf_bed.loc[:, "End"] = gtf_bed["TED"] + window_size
     gtf_bed.loc[gtf_bed["Start"] < 0, "Start"] = 0
-    #
-    # Correct the negative strand
+
+    # Handle genes on negative strand (swap TSS and TED)
     tss_neg = gtf_bed.loc[gtf_bed["Strand"] == "-", "TSS"]
     ted_neg = gtf_bed.loc[gtf_bed["Strand"] == "-", "TED"]
     gtf_bed.loc[gtf_bed["Strand"] == "-", "TSS"] = ted_neg
     gtf_bed.loc[gtf_bed["Strand"] == "-", "TED"] = tss_neg
     gtf_bed = gtf_bed.drop("Strand", axis=1)
-    #
-    # Transform the GTF to PyRanges
+
+    # Convert to PyRanges
     gtf_pr = pr.PyRanges(gtf_bed)
+
     return gtf_pr, mk_score
 
 
-# %%
-def load_marker_score(mk_score_file):
+def load_marker_score(mk_score_file: str) -> pd.DataFrame:
     """
-    Load marker scores of each cell.
+    Load marker scores from a feather file.
+
+    Parameters
+    ----------
+    mk_score_file : str
+        Path to the marker score feather file
+
+    Returns
+    -------
+    pd.DataFrame
+        DataFrame with marker scores indexed by gene names
     """
     mk_score = pd.read_feather(mk_score_file).set_index("HUMAN_GENE_SYM").rename_axis("gene_name")
     mk_score = mk_score.astype(np.float32, copy=False)
     return mk_score
 
 
-# %%
-# load mkscore get common gene
-# %%
-# load bim
-def load_bim(bfile_root, chrom):
+def load_bim(bfile_root: str, chrom: int) -> tuple[pd.DataFrame, pr.PyRanges]:
     """
-    Load the bim file.
+    Load PLINK BIM file and convert to a PyRanges object.
+
+    Parameters
+    ----------
+    bfile_root : str
+        Root path for PLINK bfiles
+    chrom : int
+        Chromosome number
+
+    Returns
+    -------
+    tuple
+        A tuple containing (bim_df, bim_pr) where:
+        - bim_df is a pandas DataFrame with BIM data
+        - bim_pr is a PyRanges object with BIM data
     """
-    bim = pd.read_csv(f"{bfile_root}.{chrom}.bim", sep="\t", header=None)
+    bim_file = f"{bfile_root}.{chrom}.bim"
+    logger.debug(f"Loading BIM file: {bim_file}")
+
+    bim = pd.read_csv(bim_file, sep="\t", header=None)
     bim.columns = ["CHR", "SNP", "CM", "BP", "A1", "A2"]
-    #
-    # Transform bim to PyRanges
+
+    # Convert to PyRanges
     bim_pr = bim.copy()
     bim_pr.columns = ["Chromosome", "SNP", "CM", "Start", "A1", "A2"]
 
+    # Adjust coordinates (BIM is 1-based, PyRanges uses 0-based)
     bim_pr["End"] = bim_pr["Start"].copy()
-    bim_pr["Start"] = bim_pr["Start"] - 1  # Due to bim file is 1-based
+    bim_pr["Start"] = bim_pr["Start"] - 1
 
     bim_pr = pr.PyRanges(bim_pr)
     bim_pr.Chromosome = f"chr{chrom}"
+
     return bim, bim_pr
 
 
-# %%
-def Overlaps_gtf_bim(gtf_pr, bim_pr):
+def overlaps_gtf_bim(gtf_pr: pr.PyRanges, bim_pr: pr.PyRanges) -> pd.DataFrame:
     """
-    Find overlaps between gtf and bim file.
+    Find overlaps between GTF and BIM data, and select nearest gene for each SNP.
+
+    Parameters
+    ----------
+    gtf_pr : pr.PyRanges
+        PyRanges object with gene coordinates
+    bim_pr : pr.PyRanges
+        PyRanges object with SNP coordinates
+
+    Returns
+    -------
+    pd.DataFrame
+        DataFrame with SNP-gene pairs where each SNP is matched to its closest gene
     """
-    # Select the overlapped regions (SNPs in gene windows)
+    # Join the PyRanges objects to find overlaps
     overlaps = gtf_pr.join(bim_pr)
     overlaps = overlaps.df
+
+    # Calculate distance to TSS
     overlaps["Distance"] = np.abs(overlaps["Start_b"] - overlaps["TSS"])
-    overlaps_small = overlaps.copy()
-    overlaps_small = overlaps_small.loc[overlaps_small.groupby("SNP").Distance.idxmin()]
-    return overlaps_small
+
+    # For each SNP, select the closest gene
+    nearest_genes = overlaps.loc[overlaps.groupby("SNP").Distance.idxmin()]
+
+    return nearest_genes
 
 
-# %%
-def filter_snps_by_keep_snp(bim_df, keep_snp_file):
-    # Load the keep_snp file and filter the BIM DataFrame
+def filter_snps_by_keep_snp(bim_df: pd.DataFrame, keep_snp_file: str) -> pd.DataFrame:
+    """
+    Filter BIM DataFrame to keep only SNPs in a provided list.
+
+    Parameters
+    ----------
+    bim_df : pd.DataFrame
+        DataFrame with BIM data
+    keep_snp_file : str
+        Path to a file with SNP IDs to keep
+
+    Returns
+    -------
+    pd.DataFrame
+        Filtered BIM DataFrame
+    """
+    # Read SNPs to keep
     keep_snp = pd.read_csv(keep_snp_file, header=None)[0].to_list()
+
+    # Filter the BIM DataFrame
     filtered_bim_df = bim_df[bim_df["SNP"].isin(keep_snp)]
+
+    logger.info(f"Kept {len(filtered_bim_df)} SNPs out of {len(bim_df)} after filtering")
+
     return filtered_bim_df
 
 
-def get_snp_counts(config):
+def get_snp_counts(config: GenerateLDScoreConfig) -> dict:
+    """
+    Count SNPs per chromosome and calculate start positions for zarr arrays.
+
+    Parameters
+    ----------
+    config : GenerateLDScoreConfig
+        Configuration object
+
+    Returns
+    -------
+    dict
+        Dictionary with SNP counts and start positions
+    """
     snp_counts = {}
     total_snp = 0
 
@@ -134,65 +234,84 @@ def get_snp_counts(config):
 
     snp_counts["total"] = total_snp
 
+    # Calculate cumulative SNP counts for zarr array indexing
     chrom_snp_length_array = np.array([snp_counts[chrom] for chrom in range(1, 23)]).cumsum()
-
     snp_counts["chrom_snp_start_point"] = [0] + chrom_snp_length_array.tolist()
 
     return snp_counts
 
 
-# %%
-def get_snp_pass_maf(bfile_root, chrom, maf_min=0.05):
+def get_snp_pass_maf(bfile_root: str, chrom: int, maf_min: float = 0.05) -> list[str]:
     """
-    Get the dummy matrix of SNP-gene pairs.
+    Get SNPs that pass the minimum minor allele frequency (MAF) threshold.
+
+    Parameters
+    ----------
+    bfile_root : str
+        Root path for PLINK bfiles
+    chrom : int
+        Chromosome number
+    maf_min : float, optional
+        Minimum MAF threshold, by default 0.05
+
+    Returns
+    -------
+    list
+        List of SNP IDs that pass the MAF threshold
     """
-    # Load the bim file
-    PlinkBIMFile = ID_List_Factory(
-        ["CHR", "SNP", "CM", "BP", "A1", "A2"], 1, ".bim", usecols=[0, 1, 2, 3, 4, 5]
+    array_snps, array_indivs, geno_array = load_bfile(
+        bfile_chr_prefix=f"{bfile_root}.{chrom}", mafMin=maf_min
     )
-    PlinkFAMFile = ID_List_Factory(["IID"], 0, ".fam", usecols=[1])
 
-    bfile = f"{bfile_root}.{chrom}"
-    snp_file, snp_obj = bfile + ".bim", PlinkBIMFile
-    array_snps = snp_obj(snp_file)
-    # m = len(array_snps.IDList)
-
-    # Load fam
-    ind_file, ind_obj = bfile + ".fam", PlinkFAMFile
-    array_indivs = ind_obj(ind_file)
+    m = len(array_snps.IDList)
     n = len(array_indivs.IDList)
-    array_file, array_obj = bfile + ".bed", PlinkBEDFileWithR2Cache
-    geno_array = array_obj(
-        array_file, n, array_snps, keep_snps=None, keep_indivs=None, mafMin=None
+    logger.info(
+        f"Loading genotype data for {m} SNPs and {n} individuals from {bfile_root}.{chrom}"
     )
-    ii = geno_array.maf > maf_min
-    snp_pass_maf = array_snps.IDList[ii]
-    print(f"After filtering SNPs with MAF < {maf_min}, {len(snp_pass_maf)} SNPs remain.")
-    return snp_pass_maf.SNP.to_list()
 
+    # Filter SNPs by MAF
+    snp_pass_maf = array_snps.IDList.iloc[geno_array.kept_snps]
+    logger.info(f"After filtering SNPs with MAF < {maf_min}, {len(snp_pass_maf)} SNPs remain")
 
-def get_ldscore(bfile_root, chrom, annot_matrix, ld_wind, ld_unit="CM"):
-    PlinkBIMFile = ID_List_Factory(
-        ["CHR", "SNP", "CM", "BP", "A1", "A2"], 1, ".bim", usecols=[0, 1, 2, 3, 4, 5]
-    )
-    PlinkFAMFile = ID_List_Factory(["IID"], 0, ".fam", usecols=[1])
+    return snp_pass_maf.SNP.to_list()
 
-    bfile = f"{bfile_root}.{chrom}"
-    snp_file, snp_obj = bfile + ".bim", PlinkBIMFile
-    array_snps = snp_obj(snp_file)
-    m = len(array_snps.IDList)
-    print(f"Read list of {m} SNPs from {snp_file}")
 
-    # Load fam
-    ind_file, ind_obj = bfile + ".fam", PlinkFAMFile
-    array_indivs = ind_obj(ind_file)
-    n = len(array_indivs.IDList)
-    print(f"Read list of {n} individuals from {ind_file}")
-    array_file, array_obj = bfile + ".bed", PlinkBEDFileWithR2Cache
-    geno_array = array_obj(
-        array_file, n, array_snps, keep_snps=None, keep_indivs=None, mafMin=None
+def get_ldscore(
+    bfile_root: str,
+    chrom: int,
+    annot_matrix: np.ndarray,
+    ld_wind: float,
+    ld_unit: str = "CM",
+    keep_snps_index: list[int] = None,
+) -> pd.DataFrame:
+    """
+    Calculate LD scores using PLINK data and an annotation matrix.
+
+    Parameters
+    ----------
+    bfile_root : str
+        Root path for PLINK bfiles
+    chrom : int
+        Chromosome number
+    annot_matrix : np.ndarray
+        Annotation matrix
+    ld_wind : float
+        LD window size
+    ld_unit : str, optional
+        Unit for the LD window, by default "CM"
+    keep_snps_index : list[int], optional
+        Indices of SNPs to keep, by default None
+
+    Returns
+    -------
+    pd.DataFrame
+        DataFrame with calculated LD scores
+    """
+    array_snps, array_indivs, geno_array = load_bfile(
+        bfile_chr_prefix=f"{bfile_root}.{chrom}", keep_snps=keep_snps_index
     )
-    # Load the annotations of the baseline
+
+    # Configure LD window based on specified unit
     if ld_unit == "SNP":
         max_dist = ld_wind
         coords = np.array(range(geno_array.m))
@@ -202,61 +321,141 @@ def get_ldscore(bfile_root, chrom, annot_matrix, ld_wind, ld_unit="CM"):
     elif ld_unit == "CM":
         max_dist = ld_wind
         coords = np.array(array_snps.df["CM"])[geno_array.kept_snps]
+        # Check if the CM is all 0
+        if np.all(coords == 0):
+            logger.warning(
+                "All CM values are 0 in the BIM file. Using 1MB window size for LD score calculation."
+            )
+            max_dist = 1_000_000
+            coords = np.array(array_snps.df["BP"])[geno_array.kept_snps]
     else:
-        raise ValueError(f"Invalid ld_wind_unit: {ld_unit}")
+        raise ValueError(f"Invalid ld_wind_unit: {ld_unit}. Must be one of: SNP, KB, CM")
+
+    # Calculate blocks for LD computation
     block_left = getBlockLefts(coords, max_dist)
-    # Calculate the LD score
-    lN_df = pd.DataFrame(geno_array.ldScoreVarBlocks(block_left, 100, annot=annot_matrix))
-    return lN_df
+    assert block_left.sum() > 0, "Invalid window size, please check the ld_wind parameter."
+
+    # Calculate LD scores
+    ld_scores = pd.DataFrame(geno_array.ldScoreVarBlocks(block_left, 100, annot=annot_matrix))
+
+    return ld_scores
 
 
-# %%
 def calculate_ldscore_from_annotation(
-    SNP_annotation_df, chrom, bfile_root, ld_wind=1, ld_unit="CM"
-):
+    snp_annotation_df: pd.DataFrame,
+    chrom: int,
+    bfile_root: str,
+    ld_wind: float = 1,
+    ld_unit: str = "CM",
+) -> pd.DataFrame:
     """
-    Calculate the SNP-gene weight matrix.
+    Calculate LD scores from SNP annotation DataFrame.
+
+    Parameters
+    ----------
+    snp_annotation_df : pd.DataFrame
+        DataFrame with SNP annotations
+    chrom : int
+        Chromosome number
+    bfile_root : str
+        Root path for PLINK bfiles
+    ld_wind : float, optional
+        LD window size, by default 1
+    ld_unit : str, optional
+        Unit for the LD window, by default "CM"
+
+    Returns
+    -------
+    pd.DataFrame
+        DataFrame with calculated LD scores
     """
-    # Get the dummy matrix
-    # Get the SNP-gene weight matrix
+    # Calculate LD scores
     snp_gene_weight_matrix = get_ldscore(
-        bfile_root, chrom, SNP_annotation_df.values, ld_wind=ld_wind, ld_unit=ld_unit
+        bfile_root, chrom, snp_annotation_df.values, ld_wind=ld_wind, ld_unit=ld_unit
     )
+
+    # Set proper data types and indices
     snp_gene_weight_matrix = snp_gene_weight_matrix.astype(np.float32, copy=False)
-    snp_gene_weight_matrix.index = SNP_annotation_df.index
-    snp_gene_weight_matrix.columns = SNP_annotation_df.columns
+    snp_gene_weight_matrix.index = snp_annotation_df.index
+    snp_gene_weight_matrix.columns = snp_annotation_df.columns
+
     return snp_gene_weight_matrix
 
 
 def calculate_ldscore_from_multiple_annotation(
-    SNP_annotation_df_list, chrom, bfile_root, ld_wind=1, ld_unit="CM"
-):
-    SNP_annotation_df = pd.concat(SNP_annotation_df_list, axis=1).astype(np.float32, copy=False)
+    snp_annotation_df_list: list[pd.DataFrame],
+    chrom: int,
+    bfile_root: str,
+    ld_wind: float = 1,
+    ld_unit: str = "CM",
+) -> list[pd.DataFrame]:
+    """
+    Calculate LD scores from multiple SNP annotation DataFrames.
+
+    Parameters
+    ----------
+    snp_annotation_df_list : list
+        List of DataFrames with SNP annotations
+    chrom : int
+        Chromosome number
+    bfile_root : str
+        Root path for PLINK bfiles
+    ld_wind : float, optional
+        LD window size, by default 1
+    ld_unit : str, optional
+        Unit for the LD window, by default "CM"
+
+    Returns
+    -------
+    list
+        List of DataFrames with calculated LD scores
+    """
+    # Combine annotations
+    combined_annotations = pd.concat(snp_annotation_df_list, axis=1).astype(np.float32, copy=False)
 
-    snp_gene_weight_matrix = get_ldscore(
-        bfile_root, chrom, SNP_annotation_df.values, ld_wind=ld_wind, ld_unit=ld_unit
+    # Calculate LD scores
+    combined_ld_scores = get_ldscore(
+        bfile_root, chrom, combined_annotations.values, ld_wind=ld_wind, ld_unit=ld_unit
     )
-    snp_gene_weight_matrix = snp_gene_weight_matrix.astype(np.float32, copy=False)
-    snp_gene_weight_matrix.index = SNP_annotation_df.index
-    snp_gene_weight_matrix.columns = SNP_annotation_df.columns
-
-    # split to each annotation
-    snp_annotation_len_list = [len(df.columns) for df in SNP_annotation_df_list]
-    snp_gene_weight_matrix_list = []
-    start = 0
-    for snp_annotation_len in snp_annotation_len_list:
-        snp_gene_weight_matrix_list.append(
-            snp_gene_weight_matrix.iloc[:, start : start + snp_annotation_len]
-        )
-        start += snp_annotation_len
-    return snp_gene_weight_matrix_list
+
+    # Apply proper indices and columns
+    combined_ld_scores.index = combined_annotations.index
+    combined_ld_scores.columns = combined_annotations.columns
+
+    # Split back into separate DataFrames
+    annotation_lengths = [len(df.columns) for df in snp_annotation_df_list]
+    result_dataframes = []
+    start_col = 0
+
+    for length in annotation_lengths:
+        end_col = start_col + length
+        result_dataframes.append(combined_ld_scores.iloc[:, start_col:end_col])
+        start_col = end_col
+
+    return result_dataframes
 
 
-# %%
-class S_LDSC_Boost:
+class LDScoreCalculator:
+    """
+    Class for calculating LD scores from gene specificity scores.
+
+    This class handles the assignment of gene specificity scores to SNPs
+    and the calculation of LD scores.
+    """
+
     def __init__(self, config: GenerateLDScoreConfig):
+        """
+        Initialize LDScoreCalculator.
+
+        Parameters
+        ----------
+        config : GenerateLDScoreConfig
+            Configuration object
+        """
         self.config = config
+        self.validate_config()
 
+        # Load marker scores
         self.mk_score = load_marker_score(config.mkscore_feather_path)
 
         # Load GTF and get common markers
@@ -264,499 +463,895 @@ class S_LDSC_Boost:
             config.gtf_annotation_file, self.mk_score, window_size=config.gene_window_size
         )
 
-        # Load enhancer
-        if config.enhancer_annotation_file is not None:
-            enhancer_df = pr.read_bed(config.enhancer_annotation_file, as_df=True)
-            enhancer_df.set_index("Name", inplace=True)
-            enhancer_df.index.name = "gene_name"
-
-            # keep the common genes and add the enhancer score
-            avg_mkscore = pd.DataFrame(self.mk_score_common.mean(axis=1), columns=["avg_mkscore"])
-            enhancer_df = enhancer_df.join(
-                avg_mkscore,
-                how="inner",
-                on="gene_name",
+        # Initialize enhancer data if provided
+        self.enhancer_pr = self._initialize_enhancer() if config.enhancer_annotation_file else None
+
+        # Initialize zarr file if needed
+        self._initialize_zarr_if_needed()
+
+    def validate_config(self):
+        """Validate configuration parameters."""
+        if not Path(self.config.mkscore_feather_path).exists():
+            raise FileNotFoundError(
+                f"Marker score file not found: {self.config.mkscore_feather_path}"
             )
 
-            # add distance to TSS
-            enhancer_df["TSS"] = self.gtf_pr.df.set_index("gene_name").reindex(enhancer_df.index)[
-                "TSS"
-            ]
+        if not Path(self.config.gtf_annotation_file).exists():
+            raise FileNotFoundError(
+                f"GTF annotation file not found: {self.config.gtf_annotation_file}"
+            )
 
-            # convert to pyranges
-            self.enhancer_pr = pr.PyRanges(enhancer_df.reset_index())
+        if (
+            self.config.enhancer_annotation_file
+            and not Path(self.config.enhancer_annotation_file).exists()
+        ):
+            raise FileNotFoundError(
+                f"Enhancer annotation file not found: {self.config.enhancer_annotation_file}"
+            )
 
-        else:
-            self.enhancer_pr = None
+    def _initialize_enhancer(self) -> pr.PyRanges:
+        """
+        Initialize enhancer data.
 
-        # create tha zarr file
-        if config.ldscore_save_format == "zarr":
-            chrom_snp_length_dict = get_snp_counts(config)
+        Returns
+        -------
+        pr.PyRanges
+            PyRanges object with enhancer data
+        """
+        # Load enhancer data
+        enhancer_df = pr.read_bed(self.config.enhancer_annotation_file, as_df=True)
+        enhancer_df.set_index("Name", inplace=True)
+        enhancer_df.index.name = "gene_name"
+
+        # Keep common genes and add marker score information
+        avg_mkscore = pd.DataFrame(self.mk_score_common.mean(axis=1), columns=["avg_mkscore"])
+        enhancer_df = enhancer_df.join(
+            avg_mkscore,
+            how="inner",
+            on="gene_name",
+        )
+
+        # Add TSS information
+        enhancer_df["TSS"] = self.gtf_pr.df.set_index("gene_name").reindex(enhancer_df.index)[
+            "TSS"
+        ]
+
+        # Convert to PyRanges
+        return pr.PyRanges(enhancer_df.reset_index())
+
+    def _initialize_zarr_if_needed(self):
+        """Initialize zarr file if zarr format is specified."""
+        if self.config.ldscore_save_format == "zarr":
+            chrom_snp_length_dict = get_snp_counts(self.config)
             self.chrom_snp_start_point = chrom_snp_length_dict["chrom_snp_start_point"]
 
-            zarr_path = Path(config.ldscore_save_dir) / f"{config.sample_name}.ldscore.zarr"
+            zarr_path = (
+                Path(self.config.ldscore_save_dir) / f"{self.config.sample_name}.ldscore.zarr"
+            )
+
             if not zarr_path.exists():
                 self.zarr_file = zarr.open(
                     zarr_path.as_posix(),
                     mode="a",
                     dtype=np.float16,
-                    chunks=config.zarr_chunk_size,
+                    chunks=self.config.zarr_chunk_size,
                     shape=(chrom_snp_length_dict["total"], self.mk_score_common.shape[1]),
                 )
-                zarr_path.mkdir(parents=True, exist_ok=True)
-                # save spot names
+                zarr_path.parent.mkdir(parents=True, exist_ok=True)
+
+                # Save metadata
                 self.zarr_file.attrs["spot_names"] = self.mk_score_common.columns.to_list()
-                # save chrom_snp_length_dict
                 self.zarr_file.attrs["chrom_snp_start_point"] = self.chrom_snp_start_point
+
             else:
                 self.zarr_file = zarr.open(zarr_path.as_posix(), mode="a")
 
     def process_chromosome(self, chrom: int):
+        """
+        Process a single chromosome to calculate LD scores.
+
+        Parameters
+        ----------
+        chrom : int
+            Chromosome number
+        """
+        logger.info(f"Processing chromosome {chrom}")
+
+        # Get SNPs passing MAF filter
         self.snp_pass_maf = get_snp_pass_maf(self.config.bfile_root, chrom, maf_min=0.05)
 
-        # Get SNP-Gene dummy pairs
-        self.snp_gene_pair_dummy = self.get_snp_gene_dummy(
+        # Get SNP-gene dummy pairs
+        self.snp_gene_pair_dummy = self._get_snp_gene_dummy(chrom)
+
+        # Apply SNP filter if provided
+        self._apply_snp_filter(chrom)
+
+        # Process additional baseline annotations if provided
+        if self.config.additional_baseline_annotation:
+            self._process_additional_baseline(chrom)
+        else:
+            # Calculate SNP-gene weight matrix
+            self.snp_gene_weight_matrix = calculate_ldscore_from_annotation(
+                self.snp_gene_pair_dummy,
+                chrom,
+                self.config.bfile_root,
+                ld_wind=self.config.ld_wind,
+                ld_unit=self.config.ld_unit,
+            )
+
+            # Apply SNP filter if needed
+            if self.keep_snp_mask is not None:
+                self.snp_gene_weight_matrix = self.snp_gene_weight_matrix[self.keep_snp_mask]
+
+        # Generate w_ld file if keep_snp_root is provided
+        if self.config.keep_snp_root:
+            self._generate_w_ld(chrom)
+
+        # Save pre-calculated SNP-gene weight matrix if requested
+        self._save_snp_gene_weight_matrix_if_needed(chrom)
+
+        # Convert to sparse matrix for memory efficiency
+        self.snp_gene_weight_matrix = csr_matrix(self.snp_gene_weight_matrix)
+        logger.info(f"SNP-gene weight matrix shape: {self.snp_gene_weight_matrix.shape}")
+
+        # Calculate baseline LD scores
+        logger.info(f"Calculating baseline LD scores for chr{chrom}")
+        self._calculate_baseline_ldscores(chrom)
+
+        # Calculate LD scores for annotation
+        logger.info(f"Calculating annotation LD scores for chr{chrom}")
+        self._calculate_annotation_ldscores(chrom)
+
+        # Clear memory
+        self._clear_memory()
+
+    def _generate_w_ld(self, chrom: int):
+        """
+        Generate w_ld file for the chromosome using filtered SNPs.
+
+        Parameters
+        ----------
+        chrom : int
+            Chromosome number
+        """
+        if not self.config.keep_snp_root:
+            logger.info(
+                f"Skipping w_ld generation for chr{chrom} as keep_snp_root is not provided"
+            )
+            return
+
+        logger.info(f"Generating w_ld for chr{chrom}")
+
+        # Get the indices of SNPs to keep based on the keep_snp_mask
+        keep_snps_index = np.nonzero(self.keep_snp_mask)[0]
+
+        # Create a simple unit annotation (all ones) for the filtered SNPs
+        unit_annotation = np.ones((len(keep_snps_index), 1))
+
+        # Calculate LD scores using the filtered SNPs
+        w_ld_scores = get_ldscore(
+            self.config.bfile_root,
             chrom,
+            unit_annotation,
+            ld_wind=self.config.ld_wind,
+            ld_unit=self.config.ld_unit,
+            keep_snps_index=keep_snps_index.tolist(),
+        )
+
+        # Load the BIM file to get SNP information
+        bim_data = pd.read_csv(
+            f"{self.config.bfile_root}.{chrom}.bim",
+            sep="\t",
+            header=None,
+            names=["CHR", "SNP", "CM", "BP", "A1", "A2"],
+        )
+
+        # Get SNP names for the kept indices
+        kept_snp_names = bim_data.iloc[keep_snps_index].SNP.tolist()
+
+        # Create the w_ld DataFrame
+        w_ld_df = pd.DataFrame(
+            {
+                "SNP": kept_snp_names,
+                "L2": w_ld_scores.values.flatten(),
+                "CHR": bim_data.iloc[keep_snps_index].CHR.values,
+                "BP": bim_data.iloc[keep_snps_index].BP.values,
+                "CM": bim_data.iloc[keep_snps_index].CM.values,
+            }
         )
 
+        # Reorder columns
+        w_ld_df = w_ld_df[["CHR", "SNP", "BP", "CM", "L2"]]
+
+        # Save to feather format
+        w_ld_dir = Path(self.config.ldscore_save_dir) / "w_ld"
+        w_ld_dir.mkdir(parents=True, exist_ok=True)
+        w_ld_file = w_ld_dir / f"weights.{chrom}.l2.ldscore.gz"
+        w_ld_df.to_csv(w_ld_file, sep="\t", index=False, compression="gzip")
+
+        logger.info(f"Saved w_ld for chr{chrom} to {w_ld_file}")
+
+    def _apply_snp_filter(self, chrom: int):
+        """
+        Apply SNP filter based on keep_snp_root.
+
+        Parameters
+        ----------
+        chrom : int
+            Chromosome number
+        """
         if self.config.keep_snp_root is not None:
-            keep_snp = pd.read_csv(f"{self.config.keep_snp_root}.{chrom}.snp", header=None)[
-                0
-            ].to_list()
+            keep_snp_file = f"{self.config.keep_snp_root}.{chrom}.snp"
+            keep_snp = pd.read_csv(keep_snp_file, header=None)[0].to_list()
             self.keep_snp_mask = self.snp_gene_pair_dummy.index.isin(keep_snp)
-            # the SNP name of keeped
             self.snp_name = self.snp_gene_pair_dummy.index[self.keep_snp_mask].to_list()
+            logger.info(f"Kept {len(self.snp_name)} SNPs after filtering with {keep_snp_file}")
+            logger.info("These filtered SNPs will be used to calculate w_ld")
         else:
             self.keep_snp_mask = None
             self.snp_name = self.snp_gene_pair_dummy.index.to_list()
+            logger.info(f"Using all {len(self.snp_name)} SNPs (no filter applied)")
+            logger.warning("No keep_snp_root provided, all SNPs will be used to calculate w_ld.")
 
-        if self.config.additional_baseline_annotation is not None:
-            additional_baseline_annotation = Path(self.config.additional_baseline_annotation)
-            additional_baseline_annotation_file_path = (
-                additional_baseline_annotation / f"baseline.{chrom}.annot.gz"
-            )
-            assert additional_baseline_annotation_file_path.exists(), (
-                f"additional_baseline_annotation_file_path not exists: {additional_baseline_annotation_file_path}"
-            )
-            additional_baseline_annotation_df = pd.read_csv(
-                additional_baseline_annotation_file_path, sep="\t"
-            )
-            additional_baseline_annotation_df.set_index("SNP", inplace=True)
-
-            # drop these columns if exists CHR         BP       CM]
-            additional_baseline_annotation_df.drop(
-                ["CHR", "BP", "CM"], axis=1, inplace=True, errors="ignore"
-            )
-
-            # reindex, for those SNPs not in additional_baseline_annotation_df, set to 0
-            num_of_not_exist_snp = (
-                ~self.snp_gene_pair_dummy.index.isin(additional_baseline_annotation_df.index)
-            ).sum()
-            if num_of_not_exist_snp > 0:
-                logger.warning(
-                    f"{num_of_not_exist_snp} SNPs not in additional_baseline_annotation_df but in the reference panel, so the additional baseline annotation of these SNP will set to 0"
-                )
-                additional_baseline_annotation_df = additional_baseline_annotation_df.reindex(
-                    self.snp_gene_pair_dummy.index, fill_value=0
-                )
-            else:
-                additional_baseline_annotation_df = additional_baseline_annotation_df.reindex(
-                    self.snp_gene_pair_dummy.index
-                )
+    def _process_additional_baseline(self, chrom: int):
+        """
+        Process additional baseline annotations.
 
-            # do this for saving the cpu time, only calculate r2 once
-            self.snp_gene_weight_matrix, additional_baseline_annotation_ldscore = (
-                calculate_ldscore_from_multiple_annotation(
-                    [self.snp_gene_pair_dummy, additional_baseline_annotation_df],
-                    chrom,
-                    self.config.bfile_root,
-                    ld_wind=self.config.ld_wind,
-                    ld_unit=self.config.ld_unit,
-                )
+        Parameters
+        ----------
+        chrom : int
+            Chromosome number
+        """
+        # Load additional baseline annotations
+        additional_baseline_path = Path(self.config.additional_baseline_annotation)
+        annot_file_path = additional_baseline_path / f"baseline.{chrom}.annot.gz"
+
+        # Verify file existence
+        if not annot_file_path.exists():
+            raise FileNotFoundError(
+                f"Additional baseline annotation file not found: {annot_file_path}"
             )
 
-            additional_baseline_annotation_ldscore = additional_baseline_annotation_ldscore.loc[
-                self.snp_name
-            ]
-            # print(additional_baseline_annotation_ldscore.index.to_list()==self.snp_name)
+        # Load annotations
+        additional_baseline_df = pd.read_csv(annot_file_path, sep="\t")
+        additional_baseline_df.set_index("SNP", inplace=True)
 
-            ld_score_file = f"{self.config.ldscore_save_dir}/additional_baseline/baseline.{chrom}.l2.ldscore.feather"
-            M_file_path = (
-                f"{self.config.ldscore_save_dir}/additional_baseline/baseline.{chrom}.l2.M"
-            )
-            M_5_file_path = (
-                f"{self.config.ldscore_save_dir}/additional_baseline/baseline.{chrom}.l2.M_5_50"
-            )
+        # Drop unnecessary columns
+        for col in ["CHR", "BP", "CM"]:
+            if col in additional_baseline_df.columns:
+                additional_baseline_df.drop(col, axis=1, inplace=True)
 
-            # save additional baseline annotation ldscore
-            self.save_ldscore_to_feather(
-                additional_baseline_annotation_ldscore.values,
-                column_names=additional_baseline_annotation_ldscore.columns,
-                save_file_name=ld_score_file,
-            )
+        # Check for SNPs not in the additional baseline
+        missing_snps = ~self.snp_gene_pair_dummy.index.isin(additional_baseline_df.index)
+        missing_count = missing_snps.sum()
 
-            # caculate the M and save
-            save_dir = Path(M_file_path).parent
-            save_dir.mkdir(parents=True, exist_ok=True)
-            M_chr_chunk = additional_baseline_annotation_df.values.sum(axis=0, keepdims=True)
-            M_5_chr_chunk = additional_baseline_annotation_df.loc[self.snp_pass_maf].values.sum(
-                axis=0, keepdims=True
-            )
-            np.savetxt(
-                M_file_path,
-                M_chr_chunk,
-                delimiter="\t",
+        if missing_count > 0:
+            logger.warning(
+                f"{missing_count} SNPs not found in additional baseline annotations. "
+                "Setting their values to 0."
             )
-            np.savetxt(
-                M_5_file_path,
-                M_5_chr_chunk,
-                delimiter="\t",
+            additional_baseline_df = additional_baseline_df.reindex(
+                self.snp_gene_pair_dummy.index, fill_value=0
             )
-
         else:
-            # Calculate SNP-Gene weight matrix
-            self.snp_gene_weight_matrix = calculate_ldscore_from_annotation(
-                self.snp_gene_pair_dummy,
+            additional_baseline_df = additional_baseline_df.reindex(self.snp_gene_pair_dummy.index)
+
+        # Calculate LD scores for both annotation sets together
+        self.snp_gene_weight_matrix, additional_ldscore = (
+            calculate_ldscore_from_multiple_annotation(
+                [self.snp_gene_pair_dummy, additional_baseline_df],
                 chrom,
                 self.config.bfile_root,
                 ld_wind=self.config.ld_wind,
                 ld_unit=self.config.ld_unit,
             )
-        # only keep the snp in keep_snp_root
-        if self.keep_snp_mask is not None:
-            self.snp_gene_weight_matrix = self.snp_gene_weight_matrix[self.keep_snp_mask]
+        )
 
-        if self.config.save_pre_calculate_snp_gene_weight_matrix:
-            snp_gene_weight_matrix_save_dir = (
-                Path(self.config.ldscore_save_dir) / "snp_gene_weight_matrix"
-            )
-            snp_gene_weight_matrix_save_dir.mkdir(parents=True, exist_ok=True)
-            logger.info(f"Saving snp_gene_weight_matrix for chr{chrom}...")
-            self.snp_gene_weight_matrix.reset_index().to_feather(
-                snp_gene_weight_matrix_save_dir / f"{chrom}.snp_gene_weight_matrix.feather"
-            )
+        # Filter additional ldscore
+        additional_ldscore = additional_ldscore.loc[self.snp_name]
 
-        # convert to sparse
-        self.snp_gene_weight_matrix = csr_matrix(self.snp_gene_weight_matrix)
-        logger.info(
-            f"Compute snp_gene_weight_matrix finished. shape: {self.snp_gene_weight_matrix.shape}"
+        # Save additional baseline LD scores
+        ld_score_file = f"{self.config.ldscore_save_dir}/additional_baseline/baseline.{chrom}.l2.ldscore.feather"
+        m_file_path = f"{self.config.ldscore_save_dir}/additional_baseline/baseline.{chrom}.l2.M"
+        m_5_file_path = (
+            f"{self.config.ldscore_save_dir}/additional_baseline/baseline.{chrom}.l2.M_5_50"
         )
+        Path(m_file_path).parent.mkdir(parents=True, exist_ok=True)
 
-        # calculate baseline ld score
-        logger.info(f"Calculating baseline ld score for chr{chrom}...")
-        self.calculate_ldscore_for_base_line(
-            chrom, self.config.sample_name, self.config.ldscore_save_dir
+        # Save LD scores
+        self._save_ldscore_to_feather(
+            additional_ldscore.values,
+            column_names=additional_ldscore.columns,
+            save_file_name=ld_score_file,
         )
 
-        # calculate ld score for annotation
-        logger.info(f"Calculating ld score for annotation for chr{chrom}...")
-        self.calculate_ldscore_use_SNP_Gene_weight_matrix_by_chr(
-            self.mk_score_common.loc[self.snp_gene_pair_dummy.columns[:-1]],
-            chrom,
-            self.config.sample_name,
-            self.config.ldscore_save_dir,
+        # Calculate and save M values
+        m_chr_chunk = additional_baseline_df.values.sum(axis=0, keepdims=True)
+        m_5_chr_chunk = additional_baseline_df.loc[self.snp_pass_maf].values.sum(
+            axis=0, keepdims=True
         )
 
-    def calculate_ldscore_use_SNP_Gene_weight_matrix_by_chunk(
-        self,
-        mk_score_chunk,
-        drop_dummy_na=True,
-    ):
-        if drop_dummy_na:
-            ldscore_chr_chunk = self.snp_gene_weight_matrix[:, :-1] @ mk_score_chunk
-        else:
-            ldscore_chr_chunk = self.snp_gene_weight_matrix @ mk_score_chunk
+        # Save M statistics
+        np.savetxt(m_file_path, m_chr_chunk, delimiter="\t")
+        np.savetxt(m_5_file_path, m_5_chr_chunk, delimiter="\t")
 
-        return ldscore_chr_chunk
+    def _save_snp_gene_weight_matrix_if_needed(self, chrom: int):
+        """
+        Save pre-calculated SNP-gene weight matrix if requested.
 
-    def save_ldscore_to_feather(self, ldscore_chr_chunk: np.ndarray, column_names, save_file_name):
-        save_dir = Path(save_file_name).parent
-        save_dir.mkdir(parents=True, exist_ok=True)
+        Parameters
+        ----------
+        chrom : int
+            Chromosome number
+        """
+        if self.config.save_pre_calculate_snp_gene_weight_matrix:
+            save_dir = Path(self.config.ldscore_save_dir) / "snp_gene_weight_matrix"
+            save_dir.mkdir(parents=True, exist_ok=True)
 
-        ldscore_chr_chunk = ldscore_chr_chunk.astype(np.float16, copy=False)
-        # avoid overflow of float16, if inf, set to max of float16
-        ldscore_chr_chunk[np.isinf(ldscore_chr_chunk)] = np.finfo(np.float16).max
-        # ldscore_chr_chunk = ldscore_chr_chunk if self.config.keep_snp_root is None else ldscore_chr_chunk[
-        #     self.keep_snp_mask]
+            logger.info(f"Saving SNP-gene weight matrix for chr{chrom}")
 
-        # save for each chunk
-        df = pd.DataFrame(
-            ldscore_chr_chunk,
-            index=self.snp_name,
-            columns=column_names,
+            save_path = save_dir / f"{chrom}.snp_gene_weight_matrix.feather"
+            self.snp_gene_weight_matrix.reset_index().to_feather(save_path)
+
+    def _calculate_baseline_ldscores(self, chrom: int):
+        """
+        Calculate and save baseline LD scores.
+
+        Parameters
+        ----------
+        chrom : int
+            Chromosome number
+        """
+        # Create baseline scores
+        baseline_mk_score = np.ones((self.snp_gene_pair_dummy.shape[1], 2))
+        baseline_mk_score[-1, 0] = 0  # all_gene column
+
+        baseline_df = pd.DataFrame(
+            baseline_mk_score, index=self.snp_gene_pair_dummy.columns, columns=["all_gene", "base"]
         )
-        df.index.name = "SNP"
-        df.reset_index().to_feather(save_file_name)
 
-    def save_ldscore_chunk_to_zarr(
-        self,
-        ldscore_chr_chunk: np.ndarray,
-        chrom: int,
-        start_col_index,
-    ):
-        ldscore_chr_chunk = ldscore_chr_chunk.astype(np.float16, copy=False)
-        # avoid overflow of float16, if inf, set to max of float16
-        ldscore_chr_chunk[np.isinf(ldscore_chr_chunk)] = np.finfo(np.float16).max
+        # Define file paths
+        ld_score_file = (
+            f"{self.config.ldscore_save_dir}/baseline/baseline.{chrom}.l2.ldscore.feather"
+        )
+        m_file = f"{self.config.ldscore_save_dir}/baseline/baseline.{chrom}.l2.M"
+        m_5_file = f"{self.config.ldscore_save_dir}/baseline/baseline.{chrom}.l2.M_5_50"
 
-        # save for each chunk
-        chrom_snp_start_point = self.chrom_snp_start_point[chrom - 1]
-        chrom_snp_end_point = self.chrom_snp_start_point[chrom]
+        # Calculate LD scores
+        ldscore_chunk = self._calculate_ldscore_from_weights(baseline_df, drop_dummy_na=False)
 
-        self.zarr_file[
-            chrom_snp_start_point:chrom_snp_end_point,
-            start_col_index : start_col_index + ldscore_chr_chunk.shape[1],
-        ] = ldscore_chr_chunk
+        # Save LD scores and M values
+        self._save_ldscore_to_feather(
+            ldscore_chunk,
+            column_names=baseline_df.columns,
+            save_file_name=ld_score_file,
+        )
 
-    def calculate_M_use_SNP_gene_pair_dummy_by_chunk(
-        self,
-        mk_score_chunk,
-        M_file_path,
-        M_5_file_path,
-        drop_dummy_na=True,
-    ):
+        self._calculate_and_save_m_values(
+            baseline_df,
+            m_file,
+            m_5_file,
+            drop_dummy_na=False,
+        )
+
+        # If keep_snp_root is not provided, use the first column of baseline ldscore as w_ld
+        if not self.config.keep_snp_root:
+            self._save_baseline_as_w_ld(chrom, ldscore_chunk)
+
+    def _save_baseline_as_w_ld(self, chrom: int, ldscore_chunk: np.ndarray):
         """
-        Calculate M use SNP_gene_pair_dummy_sumed_along_snp_axis and mk_score_chunk
+        Save the first column of baseline ldscore as w_ld.
+
+        Parameters
+        ----------
+        chrom : int
+            Chromosome number
+        ldscore_chunk : np.ndarray
+            Array with baseline LD scores
         """
-        SNP_gene_pair_dummy_sumed_along_snp_axis = self.snp_gene_pair_dummy.values.sum(
-            axis=0, keepdims=True
-        )
-        SNP_gene_pair_dummy_sumed_along_snp_axis_pass_maf = self.snp_gene_pair_dummy.loc[
-            self.snp_pass_maf
-        ].values.sum(axis=0, keepdims=True)
-        if drop_dummy_na:
-            SNP_gene_pair_dummy_sumed_along_snp_axis = SNP_gene_pair_dummy_sumed_along_snp_axis[
-                :, :-1
-            ]
-            SNP_gene_pair_dummy_sumed_along_snp_axis_pass_maf = (
-                SNP_gene_pair_dummy_sumed_along_snp_axis_pass_maf[:, :-1]
-            )
-        save_dir = Path(M_file_path).parent
-        save_dir.mkdir(parents=True, exist_ok=True)
-        M_chr_chunk = SNP_gene_pair_dummy_sumed_along_snp_axis @ mk_score_chunk
-        M_5_chr_chunk = SNP_gene_pair_dummy_sumed_along_snp_axis_pass_maf @ mk_score_chunk
-        np.savetxt(
-            M_file_path,
-            M_chr_chunk,
-            delimiter="\t",
+        logger.info(f"Using first column of baseline ldscore as w_ld for chr{chrom}")
+
+        # Create w_ld directory
+        w_ld_dir = Path(self.config.ldscore_save_dir) / "w_ld"
+        w_ld_dir.mkdir(parents=True, exist_ok=True)
+
+        # Define file path
+        w_ld_file = w_ld_dir / f"weights.{chrom}.l2.ldscore.gz"
+
+        # Extract the first column
+        w_ld_values = ldscore_chunk[:, 0]
+
+        # Create a DataFrame
+        bim_data = pd.read_csv(
+            f"{self.config.bfile_root}.{chrom}.bim",
+            sep="\t",
+            header=None,
+            names=["CHR", "SNP", "CM", "BP", "A1", "A2"],
         )
-        np.savetxt(
-            M_5_file_path,
-            M_5_chr_chunk,
-            delimiter="\t",
+        w_ld_df = pd.DataFrame(
+            {
+                "SNP": self.snp_name,
+                "L2": w_ld_values,
+            }
         )
 
-    def calculate_ldscore_use_SNP_Gene_weight_matrix_by_chr(
-        self, mk_score_common, chrom, sample_name, save_dir
-    ):
+        # Add CHR, BP, and CM information
+        w_ld_df = w_ld_df.merge(bim_data[["SNP", "CHR", "BP", "CM"]], on="SNP", how="left")
+
+        # Reorder columns
+        w_ld_df = w_ld_df[["CHR", "SNP", "BP", "CM", "L2"]]
+
+        w_ld_df.to_csv(w_ld_file, sep="\t", index=False, compression="gzip")
+
+        logger.info(f"Saved w_ld for chr{chrom} to {w_ld_file}")
+
+    def _calculate_annotation_ldscores(self, chrom: int):
         """
-        Calculate the LD score using the SNP-gene weight matrix.
-        :param sample_name:
+        Calculate and save LD scores for spatial annotations.
+
+        Parameters
+        ----------
+        chrom : int
+            Chromosome number
         """
-        # Calculate the LD score
+        # Get marker scores for gene columns (excluding dummy NA column)
+        mk_scores = self.mk_score_common.loc[self.snp_gene_pair_dummy.columns[:-1]]
+
+        # Process in chunks
         chunk_index = 1
         for i in trange(
             0,
-            mk_score_common.shape[1],
+            mk_scores.shape[1],
             self.config.spots_per_chunk,
-            desc=f"Calculating LD score by chunk for chr{chrom}",
+            desc=f"Calculating LD scores for chr{chrom}",
         ):
-            mk_score_chunk = mk_score_common.iloc[:, i : i + self.config.spots_per_chunk]
+            # Get marker scores for current chunk
+            mk_score_chunk = mk_scores.iloc[:, i : i + self.config.spots_per_chunk]
 
-            ld_score_file = f"{save_dir}/{sample_name}_chunk{chunk_index}/{sample_name}.{chrom}.l2.ldscore.feather"
-            M_file = f"{save_dir}/{sample_name}_chunk{chunk_index}/{sample_name}.{chrom}.l2.M"
-            M_5_file = (
-                f"{save_dir}/{sample_name}_chunk{chunk_index}/{sample_name}.{chrom}.l2.M_5_50"
-            )
+            # Define file paths
+            sample_name = self.config.sample_name
+            ld_score_file = f"{self.config.ldscore_save_dir}/{sample_name}_chunk{chunk_index}/{sample_name}.{chrom}.l2.ldscore.feather"
+            m_file = f"{self.config.ldscore_save_dir}/{sample_name}_chunk{chunk_index}/{sample_name}.{chrom}.l2.M"
+            m_5_file = f"{self.config.ldscore_save_dir}/{sample_name}_chunk{chunk_index}/{sample_name}.{chrom}.l2.M_5_50"
 
-            ldscore_chr_chunk = self.calculate_ldscore_use_SNP_Gene_weight_matrix_by_chunk(
-                mk_score_chunk,
-                drop_dummy_na=True,
-            )
+            # Calculate LD scores
+            ldscore_chunk = self._calculate_ldscore_from_weights(mk_score_chunk)
+
+            # Save LD scores based on format
             if self.config.ldscore_save_format == "feather":
-                self.save_ldscore_to_feather(
-                    ldscore_chr_chunk,
+                self._save_ldscore_to_feather(
+                    ldscore_chunk,
                     column_names=mk_score_chunk.columns,
                     save_file_name=ld_score_file,
                 )
             elif self.config.ldscore_save_format == "zarr":
-                self.save_ldscore_chunk_to_zarr(
-                    ldscore_chr_chunk,
+                self._save_ldscore_chunk_to_zarr(
+                    ldscore_chunk,
                     chrom=chrom,
                     start_col_index=i,
                 )
             else:
                 raise ValueError(f"Invalid ldscore_save_format: {self.config.ldscore_save_format}")
 
-            self.calculate_M_use_SNP_gene_pair_dummy_by_chunk(
+            # Calculate and save M values
+            self._calculate_and_save_m_values(
                 mk_score_chunk,
-                M_file,
-                M_5_file,
+                m_file,
+                m_5_file,
                 drop_dummy_na=True,
             )
 
             chunk_index += 1
 
-    def calculate_ldscore_for_base_line(self, chrom, sample_name, save_dir):
-        # save baseline ld score
-        baseline_mk_score = np.ones((self.snp_gene_pair_dummy.shape[1], 2))
-        baseline_mk_score[-1, 0] = 0  # all_gene
-        baseline_mk_score_df = pd.DataFrame(
-            baseline_mk_score, index=self.snp_gene_pair_dummy.columns, columns=["all_gene", "base"]
-        )
-        ld_score_file = f"{save_dir}/baseline/baseline.{chrom}.l2.ldscore.feather"
-        M_file = f"{save_dir}/baseline/baseline.{chrom}.l2.M"
-        M_5_file = f"{save_dir}/baseline/baseline.{chrom}.l2.M_5_50"
+            # Clear memory
+            del ldscore_chunk
+            gc.collect()
 
-        ldscore_chr_chunk = self.calculate_ldscore_use_SNP_Gene_weight_matrix_by_chunk(
-            baseline_mk_score_df,
-            drop_dummy_na=False,
-        )
+    def _calculate_ldscore_from_weights(
+        self, marker_scores: pd.DataFrame, drop_dummy_na: bool = True
+    ) -> np.ndarray:
+        """
+        Calculate LD scores using SNP-gene weight matrix.
+
+        Parameters
+        ----------
+        marker_scores : pd.DataFrame
+            DataFrame with marker scores
+        drop_dummy_na : bool, optional
+            Whether to drop the dummy NA column, by default True
+
+        Returns
+        -------
+        np.ndarray
+            Array with calculated LD scores
+        """
+        weight_matrix = self.snp_gene_weight_matrix
 
-        self.save_ldscore_to_feather(
-            ldscore_chr_chunk,
-            column_names=baseline_mk_score_df.columns,
-            save_file_name=ld_score_file,
-        )
-        # save baseline M
-        self.calculate_M_use_SNP_gene_pair_dummy_by_chunk(
-            baseline_mk_score_df,
-            M_file,
-            M_5_file,
-            drop_dummy_na=False,
+        if drop_dummy_na:
+            # Use all columns except the last one (dummy NA)
+            ldscore = weight_matrix[:, :-1] @ marker_scores
+        else:
+            ldscore = weight_matrix @ marker_scores
+
+        return ldscore
+
+    def _save_ldscore_to_feather(
+        self, ldscore_data: np.ndarray, column_names: list[str], save_file_name: str
+    ):
+        """
+        Save LD scores to a feather file.
+
+        Parameters
+        ----------
+        ldscore_data : np.ndarray
+            Array with LD scores
+        column_names : list
+            List of column names
+        save_file_name : str
+            Path to save the feather file
+        """
+        # Create directory if needed
+        save_dir = Path(save_file_name).parent
+        save_dir.mkdir(parents=True, exist_ok=True)
+
+        # Convert to float16 for storage efficiency
+        ldscore_data = ldscore_data.astype(np.float16, copy=False)
+
+        # Handle numerical overflow
+        ldscore_data[np.isinf(ldscore_data)] = np.finfo(np.float16).max
+
+        # Create DataFrame and save
+        df = pd.DataFrame(
+            ldscore_data,
+            index=self.snp_name,
+            columns=column_names,
         )
+        df.index.name = "SNP"
+        df.reset_index().to_feather(save_file_name)
 
-    def get_snp_gene_dummy(
+    def _save_ldscore_chunk_to_zarr(
+        self, ldscore_data: np.ndarray, chrom: int, start_col_index: int
+    ):
+        """
+        Save LD scores to a zarr array.
+
+        Parameters
+        ----------
+        ldscore_data : np.ndarray
+            Array with LD scores
+        chrom : int
+            Chromosome number
+        start_col_index : int
+            Starting column index in the zarr array
+        """
+        # Convert to float16 for storage efficiency
+        ldscore_data = ldscore_data.astype(np.float16, copy=False)
+
+        # Handle numerical overflow
+        ldscore_data[np.isinf(ldscore_data)] = np.finfo(np.float16).max
+
+        # Get start and end indices for this chromosome
+        chrom_start = self.chrom_snp_start_point[chrom - 1]
+        chrom_end = self.chrom_snp_start_point[chrom]
+
+        # Save to zarr array
+        self.zarr_file[
+            chrom_start:chrom_end,
+            start_col_index : start_col_index + ldscore_data.shape[1],
+        ] = ldscore_data
+
+    def _calculate_and_save_m_values(
         self,
-        chrom,
+        marker_scores: pd.DataFrame,
+        m_file_path: str,
+        m_5_file_path: str,
+        drop_dummy_na: bool = True,
     ):
         """
-        Get the dummy matrix of SNP-gene pairs.
+        Calculate and save M statistics.
+
+        Parameters
+        ----------
+        marker_scores : pd.DataFrame
+            DataFrame with marker scores
+        m_file_path : str
+            Path to save M values
+        m_5_file_path : str
+            Path to save M_5_50 values
+        drop_dummy_na : bool, optional
+            Whether to drop the dummy NA column, by default True
+        """
+        # Create directory if needed
+        save_dir = Path(m_file_path).parent
+        save_dir.mkdir(parents=True, exist_ok=True)
+
+        # Get sum of SNP-gene pairs
+        snp_gene_sum = self.snp_gene_pair_dummy.values.sum(axis=0, keepdims=True)
+        snp_gene_sum_maf = self.snp_gene_pair_dummy.loc[self.snp_pass_maf].values.sum(
+            axis=0, keepdims=True
+        )
+
+        # Drop dummy NA column if requested
+        if drop_dummy_na:
+            snp_gene_sum = snp_gene_sum[:, :-1]
+            snp_gene_sum_maf = snp_gene_sum_maf[:, :-1]
+
+        # Calculate M values
+        m_values = snp_gene_sum @ marker_scores
+        m_5_values = snp_gene_sum_maf @ marker_scores
+
+        # Save M values
+        np.savetxt(m_file_path, m_values, delimiter="\t")
+        np.savetxt(m_5_file_path, m_5_values, delimiter="\t")
+
+    def _get_snp_gene_dummy(self, chrom: int) -> pd.DataFrame:
+        """
+        Get dummy matrix for SNP-gene pairs.
+
+        Parameters
+        ----------
+        chrom : int
+            Chromosome number
+
+        Returns
+        -------
+        pd.DataFrame
+            DataFrame with dummy variables for SNP-gene pairs
         """
-        # Load the bim file
-        print("Loading bim data")
+        logger.info(f"Creating SNP-gene mappings for chromosome {chrom}")
+
+        # Load BIM file
         bim, bim_pr = load_bim(self.config.bfile_root, chrom)
 
+        # Determine mapping strategy
         if self.config.gene_window_enhancer_priority in ["gene_window_first", "enhancer_first"]:
-            SNP_gene_pair_gtf = self.get_SNP_gene_pair_from_gtf(
-                bim,
-                bim_pr,
-            )
-            SNP_gene_pair_enhancer = self.get_SNP_gene_pair_from_enhancer(
-                bim,
-                bim_pr,
+            # Use both gene window and enhancer
+            snp_gene_pair = self._combine_gtf_and_enhancer_mappings(bim, bim_pr)
+
+        elif self.config.gene_window_enhancer_priority is None:
+            # Use only gene window
+            snp_gene_pair = self._get_snp_gene_pair_from_gtf(bim, bim_pr)
+
+        elif self.config.gene_window_enhancer_priority == "enhancer_only":
+            # Use only enhancer
+            snp_gene_pair = self._get_snp_gene_pair_from_enhancer(bim, bim_pr)
+
+        else:
+            raise ValueError(
+                f"Invalid gene_window_enhancer_priority: {self.config.gene_window_enhancer_priority}"
             )
-            # total_SNP_gene_pair = SNP_gene_pair_gtf.join(SNP_gene_pair_enhancer, how='outer', lsuffix='_gtf', )
-
-            mask_of_nan_gtf = SNP_gene_pair_gtf.gene_name.isna()
-            mask_of_nan_enhancer = SNP_gene_pair_enhancer.gene_name.isna()
-
-            if self.config.gene_window_enhancer_priority == "gene_window_first":
-                SNP_gene_pair = SNP_gene_pair_gtf
-                SNP_gene_pair.loc[mask_of_nan_gtf, "gene_name"] = SNP_gene_pair_enhancer.loc[
-                    mask_of_nan_gtf, "gene_name"
-                ]
-            elif self.config.gene_window_enhancer_priority == "enhancer_first":
-                SNP_gene_pair = SNP_gene_pair_enhancer
-                SNP_gene_pair.loc[mask_of_nan_enhancer, "gene_name"] = SNP_gene_pair_gtf.loc[
-                    mask_of_nan_enhancer, "gene_name"
-                ]
-            else:
-                raise ValueError(
-                    f"Invalid self.config.gene_window_enhancer_priority: {self.config.gene_window_enhancer_priority}"
-                )
 
-        elif self.config.gene_window_enhancer_priority is None:  # use gtf only
-            SNP_gene_pair_gtf = self.get_SNP_gene_pair_from_gtf(
-                bim,
-                bim_pr,
+        # Save SNP-gene pair mapping
+        self._save_snp_gene_pair_mapping(snp_gene_pair, chrom)
+
+        # Create dummy variables
+        snp_gene_dummy = pd.get_dummies(snp_gene_pair["gene_name"], dummy_na=True)
+
+        return snp_gene_dummy
+
+    def _combine_gtf_and_enhancer_mappings(
+        self, bim: pd.DataFrame, bim_pr: pr.PyRanges
+    ) -> pd.DataFrame:
+        """
+        Combine gene window and enhancer mappings.
+
+        Parameters
+        ----------
+        bim : pd.DataFrame
+            BIM DataFrame
+        bim_pr : pr.PyRanges
+            BIM PyRanges object
+
+        Returns
+        -------
+        pd.DataFrame
+            Combined SNP-gene pair mapping
+        """
+        # Get mappings from both sources
+        gtf_mapping = self._get_snp_gene_pair_from_gtf(bim, bim_pr)
+        enhancer_mapping = self._get_snp_gene_pair_from_enhancer(bim, bim_pr)
+
+        # Find SNPs with missing mappings in each source
+        mask_of_nan_gtf = gtf_mapping.gene_name.isna()
+        mask_of_nan_enhancer = enhancer_mapping.gene_name.isna()
+
+        # Combine based on priority
+        if self.config.gene_window_enhancer_priority == "gene_window_first":
+            # Use gene window mappings first, fill missing with enhancer mappings
+            combined_mapping = gtf_mapping.copy()
+            combined_mapping.loc[mask_of_nan_gtf, "gene_name"] = enhancer_mapping.loc[
+                mask_of_nan_gtf, "gene_name"
+            ]
+            logger.info(
+                f"Filled {mask_of_nan_gtf.sum()} SNPs with no GTF mapping using enhancer mappings"
             )
-            SNP_gene_pair = SNP_gene_pair_gtf
 
-        elif self.config.gene_window_enhancer_priority == "enhancer_only":
-            SNP_gene_pair_enhancer = self.get_SNP_gene_pair_from_enhancer(
-                bim,
-                bim_pr,
+        elif self.config.gene_window_enhancer_priority == "enhancer_first":
+            # Use enhancer mappings first, fill missing with gene window mappings
+            combined_mapping = enhancer_mapping.copy()
+            combined_mapping.loc[mask_of_nan_enhancer, "gene_name"] = gtf_mapping.loc[
+                mask_of_nan_enhancer, "gene_name"
+            ]
+            logger.info(
+                f"Filled {mask_of_nan_enhancer.sum()} SNPs with no enhancer mapping using GTF mappings"
             )
-            SNP_gene_pair = SNP_gene_pair_enhancer
-        else:
-            raise ValueError("gtf_pr and enhancer_pr cannot be None at the same time")
 
-        # save the SNP_gene_pair to feather
-        SNP_gene_pair_save_path = (
-            Path(self.config.ldscore_save_dir) / f"SNP_gene_pair/SNP_gene_pair_chr{chrom}.feather"
-        )
-        SNP_gene_pair_save_path.parent.mkdir(parents=True, exist_ok=True)
-        SNP_gene_pair.reset_index().to_feather(SNP_gene_pair_save_path)
+        else:
+            raise ValueError(
+                f"Invalid gene_window_enhancer_priority for combining: {self.config.gene_window_enhancer_priority}"
+            )
 
-        # Get the dummy matrix
-        SNP_gene_pair_dummy = pd.get_dummies(SNP_gene_pair["gene_name"], dummy_na=True)
-        return SNP_gene_pair_dummy
+        return combined_mapping
 
-    def get_SNP_gene_pair_from_gtf(self, bim, bim_pr):
+    def _get_snp_gene_pair_from_gtf(self, bim: pd.DataFrame, bim_pr: pr.PyRanges) -> pd.DataFrame:
+        """
+        Get SNP-gene pairs based on GTF annotations.
+
+        Parameters
+        ----------
+        bim : pd.DataFrame
+            BIM DataFrame
+        bim_pr : pr.PyRanges
+            BIM PyRanges object
+
+        Returns
+        -------
+        pd.DataFrame
+            SNP-gene pairs based on GTF
+        """
         logger.info(
-            "Get SNP-gene pair from gtf, if a SNP is in multiple genes, it will be assigned to the most nearby gene (TSS)"
+            "Getting SNP-gene pairs from GTF. SNPs in multiple genes will be assigned to the nearest gene (by TSS)"
         )
-        overlaps_small = Overlaps_gtf_bim(self.gtf_pr, bim_pr)
-        # Get the SNP-gene pair
+
+        # Find overlaps between SNPs and gene windows
+        overlaps = overlaps_gtf_bim(self.gtf_pr, bim_pr)
+
+        # Get SNP information
         annot = bim[["CHR", "BP", "SNP", "CM"]]
-        SNP_gene_pair = (
-            overlaps_small[["SNP", "gene_name"]]
+
+        # Create SNP-gene pairs DataFrame
+        snp_gene_pair = (
+            overlaps[["SNP", "gene_name"]]
             .set_index("SNP")
             .join(annot.set_index("SNP"), how="right")
         )
-        return SNP_gene_pair
 
-    def get_SNP_gene_pair_from_enhancer(
-        self,
-        bim,
-        bim_pr,
-    ):
-        logger.info(
-            "Get SNP-gene pair from enhancer, if a SNP is in multiple genes, it will be assigned to the gene with highest marker score"
-        )
-        # Get the SNP-gene pair
-        overlaps_small = self.enhancer_pr.join(bim_pr).df
+        logger.info(f"Found {overlaps.shape[0]} SNP-gene pairs from GTF")
+
+        return snp_gene_pair
+
+    def _get_snp_gene_pair_from_enhancer(
+        self, bim: pd.DataFrame, bim_pr: pr.PyRanges
+    ) -> pd.DataFrame:
+        """
+        Get SNP-gene pairs based on enhancer annotations.
+
+        Parameters
+        ----------
+        bim : pd.DataFrame
+            BIM DataFrame
+        bim_pr : pr.PyRanges
+            BIM PyRanges object
+
+        Returns
+        -------
+        pd.DataFrame
+            SNP-gene pairs based on enhancer
+        """
+        if self.enhancer_pr is None:
+            raise ValueError("Enhancer annotation file is required but not provided")
+
+        # Find overlaps between SNPs and enhancers
+        overlaps = self.enhancer_pr.join(bim_pr).df
+
+        # Get SNP information
         annot = bim[["CHR", "BP", "SNP", "CM"]]
+
         if self.config.snp_multiple_enhancer_strategy == "max_mkscore":
-            logger.debug("select the gene with highest marker score")
-            overlaps_small = overlaps_small.loc[overlaps_small.groupby("SNP").avg_mkscore.idxmax()]
+            logger.info(
+                "SNPs in multiple enhancers will be assigned to the gene with highest marker score"
+            )
+            overlaps = overlaps.loc[overlaps.groupby("SNP").avg_mkscore.idxmax()]
 
         elif self.config.snp_multiple_enhancer_strategy == "nearest_TSS":
-            logger.debug("select the gene with nearest TSS")
-            overlaps_small["Distance"] = np.abs(overlaps_small["Start_b"] - overlaps_small["TSS"])
-            overlaps_small = overlaps_small.loc[overlaps_small.groupby("SNP").Distance.idxmin()]
+            logger.info("SNPs in multiple enhancers will be assigned to the gene with nearest TSS")
+            overlaps["Distance"] = np.abs(overlaps["Start_b"] - overlaps["TSS"])
+            overlaps = overlaps.loc[overlaps.groupby("SNP").Distance.idxmin()]
 
-        SNP_gene_pair = (
-            overlaps_small[["SNP", "gene_name"]]
+        # Create SNP-gene pairs DataFrame
+        snp_gene_pair = (
+            overlaps[["SNP", "gene_name"]]
             .set_index("SNP")
             .join(annot.set_index("SNP"), how="right")
         )
 
-        return SNP_gene_pair
+        logger.info(f"Found {overlaps.shape[0]} SNP-gene pairs from enhancers")
+
+        return snp_gene_pair
+
+    def _save_snp_gene_pair_mapping(self, snp_gene_pair: pd.DataFrame, chrom: int):
+        """
+        Save SNP-gene pair mapping to a feather file.
+
+        Parameters
+        ----------
+        snp_gene_pair : pd.DataFrame
+            SNP-gene pair mapping
+        chrom : int
+            Chromosome number
+        """
+        save_path = (
+            Path(self.config.ldscore_save_dir) / f"SNP_gene_pair/SNP_gene_pair_chr{chrom}.feather"
+        )
+        save_path.parent.mkdir(parents=True, exist_ok=True)
+        snp_gene_pair.reset_index().to_feather(save_path)
+
+    def _clear_memory(self):
+        """Clear memory to prevent leaks."""
+        gc.collect()
 
 
 def run_generate_ldscore(config: GenerateLDScoreConfig):
+    """
+    Main function to run the LD score generation.
+
+    Parameters
+    ----------
+    config : GenerateLDScoreConfig
+        Configuration object
+    """
+    # Create output directory
+    Path(config.ldscore_save_dir).mkdir(parents=True, exist_ok=True)
+
     if config.ldscore_save_format == "quick_mode":
         logger.info(
             "Running in quick_mode. Skip the process of generating ldscore. Using the pre-calculated ldscore."
         )
-        ldscore_save_dir = config.ldscore_save_dir
+        ldscore_save_dir = Path(config.ldscore_save_dir)
 
-        # link the baseline annotation
-        baseline_annotation_dir = Path(config.baseline_annotation_dir)
-        (ldscore_save_dir / "baseline").symlink_to(
-            baseline_annotation_dir, target_is_directory=True
-        )
+        # Set up symbolic links
+        baseline_dir = ldscore_save_dir / "baseline"
+        baseline_dir.parent.mkdir(parents=True, exist_ok=True)
+        if not baseline_dir.exists():
+            baseline_dir.symlink_to(config.baseline_annotation_dir, target_is_directory=True)
+
+        snp_gene_pair_dir = ldscore_save_dir / "SNP_gene_pair"
+        snp_gene_pair_dir.parent.mkdir(parents=True, exist_ok=True)
+        if not snp_gene_pair_dir.exists():
+            snp_gene_pair_dir.symlink_to(config.SNP_gene_pair_dir, target_is_directory=True)
+
+        # Create a done file to mark completion
+        done_file = ldscore_save_dir / f"{config.sample_name}_generate_ldscore.done"
+        done_file.touch()
 
-        # link the SNP_gene_pair
-        SNP_gene_pair_dir = Path(config.SNP_gene_pair_dir)
-        (ldscore_save_dir / "SNP_gene_pair").symlink_to(
-            SNP_gene_pair_dir, target_is_directory=True
-        )
         return
-    s_ldsc_boost = S_LDSC_Boost(config)
+
+    # Initialize calculator
+    calculator = LDScoreCalculator(config)
+
+    # Process chromosomes
     if config.chrom == "all":
+        # Process all chromosomes
         for chrom in range(1, 23):
-            s_ldsc_boost.process_chromosome(chrom)
+            try:
+                calculator.process_chromosome(chrom)
+            except Exception as e:
+                logger.error(f"Error processing chromosome {chrom}: {e}")
+                raise
     else:
-        s_ldsc_boost.process_chromosome(config.chrom)
+        # Process one chromosome
+        try:
+            chrom = int(config.chrom)
+        except ValueError:
+            logger.error(f"Invalid chromosome: {config.chrom}")
+            raise ValueError(
+                f"Invalid chromosome: {config.chrom}. Must be an integer between 1-22 or 'all'"
+            ) from None
+        else:
+            calculator.process_chromosome(chrom)
+
+    # Create a done file to mark completion
+    done_file = Path(config.ldscore_save_dir) / f"{config.sample_name}_generate_ldscore.done"
+    done_file.touch()
+
+    logger.info(f"LD score generation completed for {config.sample_name}")