smftools 0.2.1__py3-none-any.whl → 0.2.3__py3-none-any.whl

smftools/__init__.py

@@ -9,26 +9,22 @@ from . import plotting as pl
 from . import preprocessing as pp
 from . import tools as tl
 
-from . import config, datasets, hmm, readwrite
+from . import cli, config, datasets, hmm
 from .readwrite import adata_to_df, safe_write_h5ad, safe_read_h5ad, merge_barcoded_anndatas_core
 
-from .load_adata import load_adata
-
 from importlib.metadata import version
 
 package_name = "smftools"
 __version__ = version(package_name)
 
 __all__ = [
-    "load_adata"
     "adata_to_df",
     "inform",
     "ml",
     "pp",
     "tl",
     "pl",
-    "readwrite",
-    "datasets",
+    "datasets"
     "safe_write_h5ad",
     "safe_read_h5ad"
 ]

smftools/_version.py

@@ -1 +1 @@
-__version__ = "0.2.1"
+__version__ = "0.2.3"

smftools/cli/cli_flows.py

@@ -0,0 +1,94 @@
+def flow_I(config_path):
+    """
+    High-level function to call for converting raw sequencing data to an adata object. 
+    Command line accesses this through smftools load <config_path>
+    Works for nanopore pod5, fast5, and unaligned modBAM data types for direct SMF workflows.
+    Works for nanopore pod5, fast5, unaligned BAM for conversion SMF workflows.
+    Also works for illumina fastq and unaligned BAM for conversion SMF workflows.
+
+    Parameters:
+        config_path (str): A string representing the file path to the experiment configuration csv file.
+
+    Returns:
+        None
+    """
+    from ..readwrite import safe_read_h5ad, safe_write_h5ad, make_dirs
+    from ..config import LoadExperimentConfig, ExperimentConfig
+    from .load_adata import load_adata
+    from .preprocess_adata import preprocess_adata
+    from .spatial_adata import spatial_adata
+
+    import numpy as np
+    import pandas as pd
+    import anndata as ad
+    import scanpy as sc
+
+    import os
+    from importlib import resources
+    from pathlib import Path
+
+    from datetime import datetime
+    date_str = datetime.today().strftime("%y%m%d")
+    ################################### 1) General params and input organization ###################################
+    # Load experiment config parameters into global variables
+    loader = LoadExperimentConfig(config_path)
+    defaults_dir = resources.files("smftools").joinpath("config")
+    cfg, report = ExperimentConfig.from_var_dict(loader.var_dict, date_str=date_str, defaults_dir=defaults_dir)
+
+    # General config variable init - Necessary user passed inputs
+    smf_modality = cfg.smf_modality # needed for specifying if the data is conversion SMF or direct methylation detection SMF. Or deaminase smf Necessary.
+    input_data_path = Path(cfg.input_data_path)  # Path to a directory of POD5s/FAST5s or to a BAM/FASTQ file. Necessary.
+    output_directory = Path(cfg.output_directory)  # Path to the output directory to make for the analysis. Necessary.
+    fasta = Path(cfg.fasta)  # Path to reference FASTA. Necessary.
+    split_dir = Path(cfg.split_dir) # Relative path to directory for demultiplexing reads
+    split_path = output_directory / split_dir # Absolute path to directory for demultiplexing reads
+
+    # Make initial output directory
+    make_dirs([output_directory])
+
+    bam_suffix = cfg.bam_suffix
+    strands = cfg.strands
+
+    # General config variable init - Optional user passed inputs for enzyme base specificity
+    mod_target_bases = cfg.mod_target_bases  # Nucleobases of interest that may be modified. ['GpC', 'CpG', 'C', 'A']
+
+    # Conversion/deamination specific variable init
+    conversion_types = cfg.conversion_types  # 5mC
+    conversions = cfg.conversions
+
+    # Common Anndata accession params
+    reference_column = cfg.reference_column
+
+    # If conversion_types is passed:
+    if conversion_types:
+        conversions += conversion_types
+
+    ############################################### smftools load start ###############################################
+    initial_adata, initial_adata_path = load_adata(config_path)
+
+    # Initial adata path info
+    initial_backup_dir = initial_adata_path.parent / 'adata_accessory_data'
+    ############################################### smftools load end ###############################################
+
+    ############################################### smftools preprocess start ###############################################
+    pp_adata, pp_adata_path, pp_dedup_adata, pp_dup_rem_adata_path = preprocess_adata(config_path)
+
+    # Preprocessed adata path info
+    pp_adata_basename = initial_adata_path.with_suffix("").name + '_preprocessed.h5ad.gz'
+    pp_adata_path = initial_adata_path / pp_adata_basename
+    pp_backup_dir = pp_adata_path.parent / 'pp_adata_accessory_data'
+
+    # Preprocessed duplicate removed adata path info
+    pp_dup_rem_adata_basename = pp_adata_path.with_suffix("").name + '_duplicates_removed.h5ad.gz'
+    pp_dup_rem_adata_path = pp_adata_path / pp_dup_rem_adata_basename
+    pp_dup_rem_backup_dir= pp_adata_path.parent / 'pp_dup_rem_adata_accessory_data'
+    ############################################### smftools preprocess end ###############################################
+
+    ############################################### smftools spatial start ###############################################
+    # Preprocessed duplicate removed adata with basic analyses appended path info
+    basic_analyzed_adata_basename = pp_dup_rem_adata_path.with_suffix("").name + '_analyzed_I.h5ad.gz'
+    basic_analyzed_adata_path = pp_dup_rem_adata_path / basic_analyzed_adata_basename
+    basic_analyzed_backup_dir= pp_dup_rem_adata_path.parent /'duplicate_removed_analyzed_adata_I_accessory_data'
+
+    spatial_adata, spatial_adata_path = spatial_adata(config_path)
+    ############################################### smftools spatial end ###############################################

smftools/cli/hmm_adata.py

@@ -0,0 +1,338 @@
+def hmm_adata(config_path):
+    """
+    High-level function to call for hmm analysis of an adata object. 
+    Command line accesses this through smftools hmm <config_path>
+
+    Parameters:
+        config_path (str): A string representing the file path to the experiment configuration csv file.
+
+    Returns:
+        (pp_dedup_spatial_hmm_adata, pp_dedup_spatial_hmm_adata_path)
+    """
+    from ..readwrite import safe_read_h5ad, safe_write_h5ad, make_dirs, add_or_update_column_in_csv
+    from .load_adata import load_adata
+    from .preprocess_adata import preprocess_adata
+    from .spatial_adata import spatial_adata
+
+    import numpy as np
+    import pandas as pd
+    import anndata as ad
+    import scanpy as sc
+
+    import os
+    from importlib import resources
+    from pathlib import Path
+
+    from datetime import datetime
+    date_str = datetime.today().strftime("%y%m%d")
+
+    ############################################### smftools load start ###############################################
+    adata, adata_path, cfg = load_adata(config_path)
+    # General config variable init - Necessary user passed inputs
+    smf_modality = cfg.smf_modality # needed for specifying if the data is conversion SMF or direct methylation detection SMF. Or deaminase smf Necessary.
+    output_directory = Path(cfg.output_directory)  # Path to the output directory to make for the analysis. Necessary.
+
+    # Make initial output directory
+    make_dirs([output_directory])
+    ############################################### smftools load end ###############################################
+
+    ############################################### smftools preprocess start ###############################################
+    pp_adata, pp_adata_path, pp_dedup_adata, pp_dup_rem_adata_path = preprocess_adata(config_path)
+    ############################################### smftools preprocess end ###############################################
+
+    ############################################### smftools spatial start ###############################################
+    spatial_ad, spatial_adata_path = spatial_adata(config_path)
+    ############################################### smftools spatial end ###############################################
+
+    ############################################### smftools hmm start ###############################################
+    input_manager_df = pd.read_csv(cfg.summary_file)
+    initial_adata_path = Path(input_manager_df['load_adata'][0])
+    pp_adata_path = Path(input_manager_df['pp_adata'][0])
+    pp_dup_rem_adata_path = Path(input_manager_df['pp_dedup_adata'][0])
+    spatial_adata_path = Path(input_manager_df['spatial_adata'][0])
+    hmm_adata_path = Path(input_manager_df['hmm_adata'][0])
+    
+    if spatial_ad:
+        # This happens on first run of the pipeline
+        adata = spatial_ad
+    else:
+        # If an anndata is saved, check which stages of the anndata are available
+        initial_version_available = initial_adata_path.exists()
+        preprocessed_version_available = pp_adata_path.exists()
+        preprocessed_dup_removed_version_available = pp_dup_rem_adata_path.exists()
+        preprocessed_dedup_spatial_version_available = spatial_adata_path.exists()
+        preprocessed_dedup_spatial_hmm_version_available = hmm_adata_path.exists()
+
+        if cfg.force_redo_hmm_fit:
+            print(f"Forcing redo of basic analysis workflow, starting from the preprocessed adata if available. Otherwise, will use the raw adata.")
+            if preprocessed_dedup_spatial_version_available:
+                adata, load_report = safe_read_h5ad(spatial_adata_path)
+            elif preprocessed_dup_removed_version_available:
+                adata, load_report = safe_read_h5ad(pp_dup_rem_adata_path)
+            elif initial_version_available:
+                adata, load_report = safe_read_h5ad(initial_adata_path)
+            else:
+                print(f"Can not redo duplicate detection when there is no compatible adata available: either raw or preprocessed are required")
+        elif preprocessed_dedup_spatial_hmm_version_available:
+            return (None, hmm_adata_path)
+        else:
+            if preprocessed_dedup_spatial_version_available:
+                adata, load_report = safe_read_h5ad(spatial_adata_path)
+            elif preprocessed_dup_removed_version_available:
+                adata, load_report = safe_read_h5ad(pp_dup_rem_adata_path)
+            elif initial_version_available:
+                adata, load_report = safe_read_h5ad(initial_adata_path)
+            else:            
+                print(f"No adata available.")
+                return
+    references = adata.obs[cfg.reference_column].cat.categories  
+    deaminase = smf_modality == 'deaminase'        
+############################################### HMM based feature annotations ###############################################
+    if not (cfg.bypass_hmm_fit and cfg.bypass_hmm_apply):
+        from ..hmm.HMM import HMM
+        from scipy.sparse import issparse, csr_matrix
+        import warnings
+
+        pp_dir = output_directory / "preprocessed"
+        pp_dir = pp_dir / "deduplicated"
+        hmm_dir = pp_dir / "10_hmm_models"
+
+        if hmm_dir.is_dir():
+            print(f'{hmm_dir} already exists.')
+        else:
+            make_dirs([pp_dir, hmm_dir])
+
+        samples = adata.obs[cfg.sample_name_col_for_plotting].cat.categories
+        references = adata.obs[cfg.reference_column].cat.categories
+        uns_key = "hmm_appended_layers"
+
+        # ensure uns key exists (avoid KeyError later)
+        if adata.uns.get(uns_key) is None:
+            adata.uns[uns_key] = []
+
+        for sample in samples:
+            for ref in references:
+                mask = (adata.obs[cfg.sample_name_col_for_plotting] == sample) & (adata.obs[cfg.reference_column] == ref)
+                subset = adata[mask].copy()
+                if subset.shape[0] < 1:
+                    continue
+
+                for mod_site in cfg.hmm_methbases:
+                    mod_label = {'C': 'C'}.get(mod_site, mod_site)
+                    hmm_path = hmm_dir / f"{sample}_{ref}_{mod_label}_hmm_model.pth"
+
+                    # ensure the input obsm exists
+                    obsm_key = f'{ref}_{mod_label}_site'
+                    if obsm_key not in subset.obsm:
+                        print(f"Skipping {sample} {ref} {mod_label}: missing obsm '{obsm_key}'")
+                        continue
+
+                    # Fit or load model
+                    if os.path.exists(hmm_path) and not cfg.force_redo_hmm_fit:
+                        hmm = HMM.load(hmm_path)
+                        hmm.print_params()
+                    else:
+                        print(f"Fitting HMM for {sample} {ref} {mod_label}")
+                        hmm = HMM.from_config(cfg)
+                        # fit expects a list-of-seqs or 2D ndarray in the obsm
+                        seqs = subset.obsm[obsm_key]
+                        hmm.fit(seqs)
+                        hmm.print_params()
+                        hmm.save(hmm_path)
+
+                    # Apply / annotate on the subset, then copy layers back to final_adata
+                    if (not cfg.bypass_hmm_apply) or cfg.force_redo_hmm_apply:
+                        print(f"Applying HMM on subset for {sample} {ref} {mod_label}")
+                        # Use the new uns_key argument so subset will record appended layer names
+                        # (annotate_adata modifies subset.obs/layers in-place and should write subset.uns[uns_key])
+                        hmm.annotate_adata(subset,
+                                        obs_column=cfg.reference_column,
+                                        layer=cfg.layer_for_umap_plotting,
+                                        config=cfg)
+                        
+                        #to_merge = [("C_all_accessible_features", 80)]
+                        to_merge = cfg.hmm_merge_layer_features
+                        for layer_to_merge, merge_distance in to_merge:
+                            if layer_to_merge:
+                                hmm.merge_intervals_in_layer(subset,
+                                                            layer=layer_to_merge,
+                                                            distance_threshold=merge_distance,
+                                                            overwrite=True
+                                                            )
+                            else:
+                                pass
+
+                        # collect appended layers from subset.uns
+                        appended = list(subset.uns.get(uns_key, []))
+                        print(appended)
+                        if len(appended) == 0:
+                            # nothing appended for this subset; continue
+                            continue
+
+                        # copy each appended layer into adata
+                        subset_mask_bool = mask.values if hasattr(mask, "values") else np.asarray(mask)
+                        for layer_name in appended:
+                            if layer_name not in subset.layers:
+                                # defensive: skip
+                                warnings.warn(f"Expected layer {layer_name} in subset but not found; skipping copy.")
+                                continue
+                            sub_layer = subset.layers[layer_name]
+                            # ensure final layer exists and assign rows
+                            try:
+                               hmm._ensure_final_layer_and_assign(adata, layer_name, subset_mask_bool, sub_layer)
+                            except Exception as e:
+                                warnings.warn(f"Failed to copy layer {layer_name} into adata: {e}", stacklevel=2)
+                                # fallback: if dense and small, try to coerce
+                                if issparse(sub_layer):
+                                    arr = sub_layer.toarray()
+                                else:
+                                    arr = np.asarray(sub_layer)
+                                adata.layers[layer_name] = adata.layers.get(layer_name, np.zeros((adata.shape[0], arr.shape[1]), dtype=arr.dtype))
+                                final_idx = np.nonzero(subset_mask_bool)[0]
+                                adata.layers[layer_name][final_idx, :] = arr
+
+                        # merge appended layer names into adata.uns
+                        existing = list(adata.uns.get(uns_key, []))
+                        for ln in appended:
+                            if ln not in existing:
+                                existing.append(ln)
+                        adata.uns[uns_key] = existing
+
+    else:
+        pass
+    
+    ## Save HMM annotated adata
+    if not hmm_adata_path.exists():
+        print('Saving hmm analyzed adata post preprocessing and duplicate removal')
+        if ".gz" == hmm_adata_path.suffix:
+            safe_write_h5ad(adata, hmm_adata_path, compression='gzip', backup=True)
+        else:
+            hmm_adata_path = hmm_adata_path.with_name(hmm_adata_path.name + '.gz')
+            safe_write_h5ad(adata, hmm_adata_path, compression='gzip', backup=True)
+
+    add_or_update_column_in_csv(cfg.summary_file, "hmm_adata", hmm_adata_path)
+
+    ########################################################################################################################
+
+############################################### HMM based feature plotting ###############################################
+    
+    hmm_dir = pp_dir / "11_hmm_clustermaps"
+
+    if hmm_dir.is_dir():
+        print(f'{hmm_dir} already exists.')
+    else:
+        make_dirs([pp_dir, hmm_dir])
+        from ..plotting import combined_hmm_raw_clustermap
+        feature_layers = [
+            "all_accessible_features",
+            "large_accessible_patch",
+            "small_bound_stretch",
+            "medium_bound_stretch",
+            "putative_nucleosome",
+            "all_accessible_features_merged",
+        ]
+
+        layers: list[str] = []
+
+        if any(base in ["C", "CpG", "GpC"] for base in cfg.mod_target_bases):
+            if smf_modality == 'deaminase':
+                layers.extend([f"C_{layer}" for layer in feature_layers])
+            elif smf_modality == 'conversion':
+                layers.extend([f"GpC_{layer}" for layer in feature_layers])
+
+        if 'A' in cfg.mod_target_bases:
+            layers.extend([f"A_{layer}" for layer in feature_layers])
+
+        if not layers:
+            raise ValueError(
+                f"No HMM feature layers matched mod_target_bases={cfg.mod_target_bases} "
+                f"and smf_modality={smf_modality}"
+            )
+        
+        if smf_modality == 'direct':
+            sort_by = "any_a"
+        else:
+            sort_by = 'gpc'
+
+        for layer in layers:
+            save_path = hmm_dir / layer
+            make_dirs([save_path])
+
+            combined_hmm_raw_clustermap(
+            adata,
+            sample_col=cfg.sample_name_col_for_plotting,
+            reference_col=cfg.reference_column,
+            hmm_feature_layer=layer,
+            layer_gpc="nan0_0minus1",
+            layer_cpg="nan0_0minus1",
+            layer_any_c="nan0_0minus1",
+            layer_a= "nan0_0minus1",
+            cmap_hmm="coolwarm",
+            cmap_gpc="coolwarm",
+            cmap_cpg="viridis",
+            cmap_any_c='coolwarm',
+            cmap_a= "coolwarm",
+            min_quality=cfg.read_quality_filter_thresholds[0],
+            min_length=cfg.read_len_filter_thresholds[0],
+            min_mapped_length_to_reference_length_ratio=cfg.read_len_to_ref_ratio_filter_thresholds[0],
+            min_position_valid_fraction=1-cfg.position_max_nan_threshold,
+            save_path=save_path,
+            normalize_hmm=False,
+            sort_by=sort_by,  # options: 'gpc', 'cpg', 'gpc_cpg', 'none', or 'obs:<column>'
+            bins=None,
+            deaminase=deaminase,
+            min_signal=0
+            )
+
+    hmm_dir = pp_dir / "12_hmm_bulk_traces"
+
+    if hmm_dir.is_dir():
+        print(f'{hmm_dir} already exists.')
+    else:
+        make_dirs([pp_dir, hmm_dir])
+        from ..plotting import plot_hmm_layers_rolling_by_sample_ref
+        saved = plot_hmm_layers_rolling_by_sample_ref(
+            adata,
+            layers=adata.uns['hmm_appended_layers'],
+            sample_col=cfg.sample_name_col_for_plotting,
+            ref_col=cfg.reference_column,
+            window=101,
+            rows_per_page=4,
+            figsize_per_cell=(4,2.5),
+            output_dir=hmm_dir,
+            save=True,
+            show_raw=False
+        )
+
+    hmm_dir = pp_dir / "13_hmm_fragment_distributions"
+
+    if hmm_dir.is_dir():
+        print(f'{hmm_dir} already exists.')
+    else:
+        make_dirs([pp_dir, hmm_dir])
+        from ..plotting import plot_hmm_size_contours
+
+        for layer, max in [('C_all_accessible_features_lengths', 400), ('C_all_footprint_features_lengths', 160), ('C_all_accessible_features_merged_lengths', 800)]:
+            save_path = hmm_dir / layer
+            make_dirs([save_path])
+
+            figs = plot_hmm_size_contours(
+                adata,
+                length_layer=layer,
+                sample_col=cfg.sample_name_col_for_plotting,
+                ref_obs_col=cfg.reference_column,
+                rows_per_page=6,
+                max_length_cap=max,
+                figsize_per_cell=(3.5, 2.2),
+                save_path=save_path,
+                save_pdf=False,
+                save_each_page=True,
+                dpi=200,
+                smoothing_sigma=None,
+                normalize_after_smoothing=False,
+                cmap='viridis', 
+                log_scale_z=True
+            )
+    ########################################################################################################################
+
+    return (adata, hmm_adata_path)