pg-sui 0.2.3__py3-none-any.whl → 1.6.16a3__py3-none-any.whl

simulation/sim_benchmarks.py

@@ -1,333 +0,0 @@
-#!/usr/bin/env python
-import sys
-import os
-import subprocess
-import errno
-
-import toytree
-import toyplot.pdf
-import pyvolve
-import copy
-import random
-import re
-import numpy as np
-import pandas as pd
-
-import matplotlib.pyplot as plt
-
-def main():
-    """
-    Using pyvolve and toytree to simulate data for PG-SUI
-
-    Generates random data matrices w/ varying dimensions
-    for the purposes of runtime benchmarking
-
-    """
-    seed=553423
-    random.seed(seed)
-
-    num_samples_range=[10, 100, 1000]
-    num_loci_range=[100, 1000, 10000]
-    loc_length=100
-    write_gene_alignments=False
-    make_gene_trees=False
-    make_guidetrees=True #set to true to run IQTREE on simulated SNP matrices
-    keep_all=False #set to true to keep ALL iqtree outputs
-    keep_report=True #set to true to keep .iqtree files
-    get_siterates=True #set to true to infer site-specific rates in IQTREE
-    snps_per_locus=1
-    iqtree_bin="iqtree2"
-    get_rates=True
-    iq_procs=2
-
-    ###################
-
-    if get_siterates and not make_guidetrees:
-        print("ERROR: can't set get_siterates=True and make_guidetrees=False")
-        print("Setting make_guidetrees=True and proceeding...")
-        make_guidetrees=True
-
-    for num_samples in num_samples_range:
-        outgroup="r0"
-        tobj = toytree.rtree.unittree(ntips=num_samples,
-                                    treeheight=1.0,
-                                    random_names=False,
-                                    seed=random.randint(1, (sys.maxsize * 2 + 1)))
-        guidetree=tobj.write(tree_format=5)
-        for num_loci in num_loci_range:
-            print("num_samples:",num_samples)
-            print("num_loci:",num_loci)
-            pass
-
-            base="benchmark_"+"i"+str(num_samples)+"_l"+str(num_loci)
-            tobj.write((base+"_guidetree.tre"))
-
-            data=dict()
-            for ind in tobj.get_tip_labels():
-                data[ind] = list()
-
-            my_tree = pyvolve.read_tree(tree=guidetree)
-
-
-            #for model in ["gtr","gtrgamma"]:
-            for model in ["gtrgamma"]:
-                model_outpath=base+"_"+model
-
-                for locus in range(num_loci):
-                    print(locus)
-                    f = np.random.random(4)
-                    f /= f.sum()
-                    parameters = {
-                    "mu":
-                        {"AC": np.random.uniform(low=0.0, high=1.0),
-                        "AG": np.random.uniform(low=0.0, high=1.0),
-                        "AT": np.random.uniform(low=0.0, high=1.0),
-                        "CG": np.random.uniform(low=0.0, high=1.0),
-                        "CT": np.random.uniform(low=0.0, high=1.0),
-                        "GT": np.random.uniform(low=0.0, high=1.0)},
-                    "state_freqs":
-                        [f[0], f[1], f[2], f[3]]
-                    }
-                    if model == "gtr":
-                        #GTR model, without rate heterogeneity
-                        my_model = pyvolve.Model("nucleotide",
-                            parameters)
-                    else:
-                        my_model = pyvolve.Model("nucleotide",
-                            parameters,
-                            rate_factors = [
-                                        np.random.uniform(low=0.1, high=0.7, size=1),
-                                        np.random.uniform(low=0.5, high=1.2, size=1),
-                                        np.random.uniform(low=1.0, high=1.8, size=1),
-                                        np.random.uniform(low=1.5, high=5.0, size=1)
-                                        ],
-                            rate_probs = [0.4, 0.3, 0.2, 0.1] )
-                    if write_gene_alignments:
-                        fasta_outpath="full_alignments/"
-                        if not os.path.exists(fasta_outpath):
-                            os.mkdir(fasta_outpath)
-                    else:
-                        fasta_outpath=model_outpath
-                    fastaout=fasta_outpath +model_outpath+"_loc"+str(locus) + "_gene-alignment.fasta"
-                    #sample a gene alignment
-                    loc = sample_locus(my_tree, my_model, loc_length, snps_per_locus, fastaout)
-
-                    if loc:
-                        #sample SNP(s) from gene alignment
-                        sampled = sample_snp(read_fasta(fastaout), loc_length, snps_per_locus)
-                        if sampled is not None:
-                            data = add_locus(data,sampled)
-
-                        if not write_gene_alignments:
-                            os.remove(fastaout)
-                            if make_gene_trees:
-                                print("ERROR: Can't make gene trees when write_gene_alignments = False")
-                        elif make_gene_trees:
-                            run_iqtree(fastaout,
-                                iqtree_path=iqtree_bin,
-                                keep_all=keep_all,
-                                keep_report=keep_report,
-                                rates=get_siterates,
-                                procs=iq_procs)
-                            reroot_tree(tree=(fastaout+".treefile"),
-                                rooted=(fastaout+".rooted.tre"),
-                                outgroup_wildcard=outgroup)
-
-                #write full SNP alignment & generate tree
-                all_snp_out=model_outpath+"_base-snps-concat.fasta"
-                write_fasta(data, all_snp_out)
-                if make_guidetrees:
-                    run_iqtree(all_snp_out,
-                        iqtree_path=iqtree_bin,
-                        keep_all=keep_all,
-                        keep_report=keep_report,
-                        rates=get_siterates,
-                        procs=iq_procs)
-                    reroot_tree(tree=(all_snp_out+".treefile"),
-                        rooted=(all_snp_out+".rooted.tre"),
-                        outgroup_wildcard=outgroup)
-
-def reroot_tree(tree, rooted="out.rooted.tre", outgroup_wildcard="out"):
-    t=toytree.tree(tree)
-    try:
-        rt=t.root(wildcard=outgroup_wildcard)
-        rt.write(rooted, tree_format=5)
-        return(rt)
-    except Exception:
-        t.write(rooted, tree_format=5)
-        return(None)
-
-
-def hybridization(dat, prob=0.1, source=None, target=None):
-    new_dat=dict()
-    if source is None:
-        source = [key for key in dat.keys()]
-    if target is None:
-        target = [key for key in dat.keys()]
-
-    for individual in dat.keys():
-        new_dat[individual] = dat[individual]
-        aln_len=len(dat[individual])
-    all_indices=list(range(aln_len))
-    num=int(aln_len*prob)
-
-    for target_individual in target:
-        snp_indices = np.random.choice(all_indices, size=num, replace=False)
-        for index in snp_indices:
-            source_ind=np.random.choice(source, size=1)[0]
-            new_dat[target_individual][index] = new_dat[source_ind][index]
-    return(new_dat)
-
-def run_iqtree(aln,
-    iqtree_path="iqtree",
-    keep_all=False,
-    keep_report=False,
-    outgroup=None,
-    rates=False,
-    procs=4):
-    #run
-    cmd = [iqtree_path,
-                    "-s",
-                    str(aln),
-                    "-m",
-                    "GTR+I*G4",
-                    "-redo",
-                    "-T",
-                    str(procs)
-                    ]
-    if outgroup is not None:
-        cmd.append("-o")
-        cmd.append(str(outgroup))
-    if rates:
-        #use -wst (NOT -mlrate) if using iq-tree 1.6xx
-        #cmd.append("-wsr")
-        cmd.append("--mlrate")
-    result = subprocess.run(cmd, capture_output=True, text=True)
-    #print(result.stdout)
-    #print(result.stderr)
-
-    if not keep_all:
-        #delete everything except treefile
-        silentremove((aln + ".bionj"))
-        silentremove((aln + ".ckp.gz"))
-        silentremove((aln + ".log"))
-        silentremove((aln + ".mldist"))
-        silentremove((aln + ".uniqueseq.phy"))
-        if not keep_report:
-            silentremove((aln + ".iqtree"))
-    return((aln + ".treefile"))
-
-def add_locus(d, new):
-    for sample in d.keys():
-        for snp in new[sample]:
-            d[sample].append(snp)
-    return(d)
-
-def write_fasta(seqs, fas):
-	with open(fas, 'w') as fh:
-		#Write seqs to FASTA first
-		for a in seqs.keys():
-			name = ">" + str(a) + "\n"
-			seq = "".join(seqs[a]) + "\n"
-			fh.write(name)
-			fh.write(seq)
-		fh.close()
-
-def read_fasta(fasta):
-    data = dict()
-    header=False
-    sample=None
-    sequence=""
-    with open(fasta, "r") as fin:
-        for line in fin:
-            line = line.strip()
-            if not line:  # If blank line.
-                continue
-            if line[0] == ">":
-                if sample:
-                    data[sample] = sequence
-                    sequence = ""
-                sample=line[1:]
-            else:
-                sequence = sequence + line
-        data[sample] = sequence
-        return(data)
-
-def sample_snp(aln_dict, aln_len, snps_per_locus=1):
-    snp_indices = []
-    snp_aln = dict()
-    if aln_len == 1:
-        for sample in aln_dict.keys():
-            snp_aln[sample] = aln_dict[sample][0]
-        return(snp_aln)
-    else:
-        for sample in aln_dict.keys():
-            snp_aln[sample] = []
-    for i in range(aln_len):
-        vars=[]
-        for sample in aln_dict.keys():
-            nuc=aln_dict[sample][i]
-            if len(vars) == 0:
-                vars.append(nuc)
-            elif nuc not in vars:
-                snp_indices.append(i)
-                break
-    if len(snp_indices) == 0:
-        return(None)
-    elif len(snp_indices) == 1:
-        #sample them all
-        for sample in aln_dict.keys():
-            snp_aln[sample] = aln_dict[sample][snp_indices[0]]
-    else:
-        sampled_indices = np.random.choice(snp_indices, size=snps_per_locus, replace=False)
-        for sample in aln_dict.keys():
-            for i in sampled_indices:
-                snp_aln[sample].append(aln_dict[sample][i])
-    return(snp_aln)
-
-def sample_locus(tree, model, gene_len=1000, num_snps=1, out="out.fasta"):
-    try:
-        my_partition = pyvolve.Partition(models = model, size=gene_len)
-        my_evolver = pyvolve.Evolver(partitions = my_partition, tree = tree)
-        my_evolver(seqfile = out,
-            seqfmt = "fasta",
-            ratefile=False,
-            infofile=False)
-        return(True)
-    except Exception:
-        return False
-
-def silentremove(filename):
-    try:
-        os.remove(filename)
-    except OSError as e: # this would be "except OSError, e:" before Python 2.6
-        if e.errno != errno.ENOENT: # errno.ENOENT = no such file or directory
-            raise # re-raise exception if a different error occurred
-
-def get_tree_tips(tree):
-    tips = re.split('[ ,\(\);]', tree)
-    return([i for i in tips if i])
-
-def basic_tree_plot(tree, out="out.pdf"):
-    mystyle = {
-        "edge_type": "p",
-        "edge_style": {
-            "stroke": toytree.colors[0],
-            "stroke-width": 1,
-        },
-        "tip_labels_align": True,
-        "tip_labels_style": {"font-size": "5px"},
-        "node_labels": False,
-        "tip_labels": True
-    }
-
-    canvas, axes, mark = tree.draw(
-        width=400,
-        height=600,
-        **mystyle,
-    )
-
-    toyplot.pdf.render(canvas, out)
-
-if __name__ == "__main__":
-    main()