Binning stats/taxonomy summary

autometa/binning/recursive_dbscan.py

@@ -83,12 +83,11 @@ def add_metrics(df, markers_df, domain="bacteria"):
     clusters = dict(list(df.groupby("cluster")))
     metrics = {"purity": {}, "completeness": {}}
     for cluster, dff in clusters.items():
-        contigs = dff.index.tolist()
-        summed_markers = markers_df[markers_df.index.isin(contigs)].sum()
-        is_present = summed_markers >= 1
-        is_single_copy = summed_markers == 1
-        nunique_markers = summed_markers[is_present].index.nunique()
-        num_single_copy_markers = summed_markers[is_single_copy].index.nunique()
+        pfam_counts = markers_df[markers_df.index.isin(dff.index)].sum()
+        is_present = pfam_counts >= 1
+        is_single_copy = pfam_counts == 1
+        nunique_markers = pfam_counts[is_present].count()
+        num_single_copy_markers = pfam_counts[is_single_copy].count()
         completeness = nunique_markers / expected_number * 100
         # Protect from divide by zero
         if nunique_markers == 0:

autometa/binning/summary.py

@@ -0,0 +1,365 @@
+#!/usr/bin/env python
+# -*- coding: utf-8 -*-
+"""
+COPYRIGHT
+Copyright 2020 Ian J. Miller, Evan R. Rees, Kyle Wolf, Siddharth Uppal,
+Shaurya Chanana, Izaak Miller, Jason C. Kwan
+
+This file is part of Autometa.
+
+Autometa is free software: you can redistribute it and/or modify
+it under the terms of the GNU Affero General Public License as published by
+the Free Software Foundation, either version 3 of the License, or
+(at your option) any later version.
+
+Autometa is distributed in the hope that it will be useful,
+but WITHOUT ANY WARRANTY; without even the implied warranty of
+MERCHANTABILITY or FITNESS FOR A PARTICULAR PURPOSE. See the
+GNU Affero General Public License for more details.
+
+You should have received a copy of the GNU Affero General Public License
+along with Autometa. If not, see <http://www.gnu.org/licenses/>.
+COPYRIGHT
+
+Script to summarize/write Autometa binning results
+"""
+
+
+import logging
+import os
+import tempfile
+
+import pandas as pd
+import numpy as np
+
+from Bio import SeqIO
+from Bio.SeqUtils import GC
+from glob import glob
+
+from autometa import config
+from autometa.taxonomy.ncbi import NCBI
+from autometa.taxonomy.majority_vote import rank_taxids
+from autometa.common.metabin import MetaBin
+from autometa.common.markers import Markers
+
+
+logger = logging.getLogger(__name__)
+
+
+def get_gc_content(metagenome):
+    gc_content = [
+        {"contig": rec.id, "GC": GC(rec.seq)}
+        for rec in SeqIO.parse(metagenome, "fasta")
+    ]
+    df = pd.DataFrame(gc_content).set_index("contig")
+    return df
+
+
+def merge_annotations(mgargs):
+    """Merge all required annotations for binning summaries.
+
+    Parameters
+    ----------
+    mgargs : argparse.Namespace
+        metagenome args parsed from config using `config.parse_config`.
+
+    Returns
+    -------
+    pd.DataFrame
+        index=contig, cols=['cluster','length','coverage','taxid', *canonical_ranks]
+
+    Raises
+    ------
+    FileNotFoundError
+        One of lengths.tsv or coverages.tsv does not exist.
+    """
+    binning_fpaths = {
+        "bacteria": mgargs.files.bacteria_binning,
+        "archaea": mgargs.files.archaea_binning,
+    }
+    gc_df = get_gc_content(metagenome=mgargs.files.metagenome)
+    dataframes = [gc_df]
+    for fpath in [mgargs.files.lengths, mgargs.files.coverages]:
+        if not os.path.exists(fpath):
+            raise FileNotFoundError(fpath)
+        df = pd.read_csv(fpath, sep="\t", index_col="contig")
+        dataframes.append(df)
+    if os.path.exists(mgargs.files.taxonomy):
+        df = pd.read_csv(mgargs.files.taxonomy, sep="\t", index_col="contig")
+        dataframes.append(df)
+    annotations = {}
+    for domain, fpath in binning_fpaths.items():
+        if not os.path.exists(fpath) or not os.path.getsize(fpath):
+            bin_df = pd.DataFrame()
+        else:
+            bin_df = pd.read_csv(fpath, sep="\t", index_col="contig")
+            for df in dataframes:
+                bin_df = pd.merge(
+                    bin_df, df, how="left", left_index=True, right_index=True
+                )
+        annotations.update({domain: bin_df})
+    return annotations
+
+
+def write_cluster_records(bin_df, metagenome, outdir):
+    """Write clusters to `outdir` given clusters `df` and metagenome `records`
+
+    Parameters
+    ----------
+    bin_df : pd.DataFrame
+        Autometa binning dataframe. index='contig', cols=['cluster', ...]
+    metagenome : str
+        Path to metagenome fasta file
+    outdir : str
+        Path to output directory to write MetaBin fastas
+
+    """
+    if not os.path.isdir(outdir):
+        os.makedirs(outdir)
+    mgrecords = [rec for rec in SeqIO.parse(metagenome, "fasta")]
+    for cluster, dff in bin_df.fillna(value={"cluster": "unclustered"}).groupby(
+        "cluster"
+    ):
+        contigs = set(dff.index)
+        records = [rec for rec in mgrecords if rec.id in contigs]
+        outfpath = os.path.join(outdir, f"{cluster}.fna")
+        SeqIO.write(records, outfpath, "fasta")
+    return
+
+
+def fragmentation_metric(df, quality_measure=0.50):
+    """Describes the quality of assembled genomes that are fragmented in
+        contigs of different length.
+
+        For more information see:
+            http://www.metagenomics.wiki/pdf/definition/assembly/n50
+
+        Parameters
+        ----------
+
+        quality_measure : 0 < float < 1
+            Description of parameter `quality_measure` (the default is .50).
+            I.e. default measure is N50, but could use .1 for N10 or .9 for N90
+
+        Returns
+        -------
+        int
+            Minimum contig length to cover `quality_measure` of genome (i.e. percentile contig length)
+
+        """
+    target_size = df.length.sum() * quality_measure
+    lengths = 0
+    for length in df.length.sort_values(ascending=False):
+        lengths += length
+        if lengths > target_size:
+            return length
+
+
+def get_metabin_stats(bin_df, markers_fpath, assembly):
+    """Retrieve statistics for all clusters recovered from Autometa binning.
+
+    Parameters
+    ----------
+    bin_df : pd.DataFrame
+        Autometa binning table. index=contig, cols=['cluster','length', 'GC', 'coverage', ...]
+    markers_fpath : str
+        </path/to/{domain}.markers.tsv
+    assembly : str
+        </path/to/corresponding/metagenome/assembly.fna
+
+    Returns
+    -------
+    pd.DataFrame
+        dataframe consisting of various metabin statistics indexed by cluster.
+    """
+    stats = []
+    markers_df = Markers.load(markers_fpath)
+    for cluster, dff in bin_df.fillna(value={"cluster": "unclustered"}).groupby(
+        "cluster"
+    ):
+        contigs = set(dff.index)
+        length_weighted_coverage = np.average(
+            a=dff.coverage, weights=dff.length / dff.length.sum()
+        )
+        length_weighted_gc = np.average(a=dff.GC, weights=dff.length / dff.length.sum())
+        num_expected_markers = markers_df.shape[1]
+        pfam_counts = markers_df.loc[markers_df.index.isin(dff.index)].sum()
+        if pfam_counts.empty:
+            total_markers = 0
+            num_single_copy_markers = 0
+            num_markers_present = 0
+            completeness = pd.NA
+            purity = pd.NA
+        else:
+            total_markers = pfam_counts.sum()
+            num_single_copy_markers = pfam_counts[pfam_counts == 1].count()
+            num_markers_present = pfam_counts[pfam_counts >= 1].count()
+            completeness = num_markers_present / num_expected_markers * 100
+            purity = num_single_copy_markers / num_markers_present * 100
+
+        stats.append(
+            {
+                "cluster": cluster,
+                "nseqs": dff.shape[0],
+                "seqs_pct": dff.shape[0] / bin_df.shape[0] * 100,
+                "size (bp)": dff.length.sum(),
+                "size_pct": dff.length.sum() / bin_df.length.sum() * 100,
+                "N90": fragmentation_metric(dff, quality_measure=0.9),
+                "N50": fragmentation_metric(dff, quality_measure=0.5),
+                "N10": fragmentation_metric(dff, quality_measure=0.1),
+                "length_weighted_gc": length_weighted_gc,
+                "min_GC": dff.GC.min(),
+                "max_GC": dff.GC.max(),
+                "std_GC": dff.GC.std(),
+                "length_weighted_coverage": length_weighted_coverage,
+                "min_coverage": dff.coverage.min(),
+                "max_coverage": dff.coverage.max(),
+                "std_coverage": dff.coverage.max(),
+                "completeness": completeness,
+                "purity": purity,
+                "num_total_markers": total_markers,
+                f"num_unique_markers (expected {num_expected_markers})": num_markers_present,
+                "num_single_copy_markers": num_single_copy_markers,
+            }
+        )
+    stats_df = pd.DataFrame(stats)
+    stats_df.set_index("cluster", inplace=True)
+    return stats_df
+
+
+def get_metabin_taxonomies(bin_df, ncbi):
+    """Retrieve taxonomies of all clusters recovered from Autometa binning.
+
+    Parameters
+    ----------
+    bin_df : pd.DataFrame
+        Autometa binning table. index=contig, cols=['cluster','length','taxid', *canonical_ranks]
+    ncbi : autometa.taxonomy.ncbi.NCBI instance
+        Autometa NCBI class instance
+
+    Returns
+    -------
+    pd.DataFrame
+        Dataframe consisting of cluster taxonomy with taxid and canonical rank.
+        Indexed by cluster
+    """
+    canonical_ranks = ncbi.CANONICAL_RANKS
+    if "root" in canonical_ranks:
+        canonical_ranks.remove("root")
+    is_clustered = bin_df.cluster.notnull()
+    bin_df = bin_df[is_clustered]
+    tmpfpath = tempfile.mktemp()
+    outcols = ["cluster", "length", "taxid", *canonical_ranks]
+    bin_df[outcols].to_csv(tmpfpath, sep="\t", index=False, header=False)
+    taxonomies = {}
+    with open(tmpfpath) as fh:
+        for line in fh:
+            llist = line.strip().split("\t")
+            cluster = llist[0]
+            length = int(llist[1])
+            taxid = int(llist[2])
+            ranks = llist[3:]
+            for rank, canonical_rank in zip(ranks, canonical_ranks):
+                if rank != "unclassified":
+                    break
+            if cluster not in taxonomies:
+                taxonomies.update({cluster: {canonical_rank: {taxid: length}}})
+            elif canonical_rank not in taxonomies[cluster]:
+                taxonomies[cluster].update({canonical_rank: {taxid: length}})
+            elif taxid not in taxonomies[cluster][canonical_rank]:
+                taxonomies[cluster][canonical_rank].update({taxid: length})
+            else:
+                taxonomies[cluster][canonical_rank][taxid] += length
+    os.remove(tmpfpath)
+    cluster_taxonomies = rank_taxids(taxonomies, ncbi)
+    cluster_taxa_df = pd.Series(data=cluster_taxonomies, name="taxid").to_frame()
+    lineage_df = ncbi.get_lineage_dataframe(cluster_taxa_df.taxid.tolist(), fillna=True)
+    cluster_taxa_df = pd.merge(
+        cluster_taxa_df, lineage_df, how="left", left_on="taxid", right_index=True
+    )
+    cluster_taxa_df.index.name = "cluster"
+    return cluster_taxa_df
+
+
+def main():
+    import argparse
+    import logging as logger
+
+    logger.basicConfig(
+        format="[%(asctime)s %(levelname)s] %(name)s: %(message)s",
+        datefmt="%m/%d/%Y %I:%M:%S %p",
+        level=logger.DEBUG,
+    )
+    parser = argparse.ArgumentParser(
+        description="Summarize Autometa results writing genome fastas and their respective"
+        " taxonomies/assembly metrics for respective metagenomes",
+        formatter_class=argparse.ArgumentDefaultsHelpFormatter,
+    )
+    parser.add_argument(
+        "workspace", help="Path to Autometa results workspace directory",
+    )
+    parser.add_argument(
+        "--write",
+        help="Write autometa clustered metabins",
+        action="store_true",
+        default=False,
+    )
+    args = parser.parse_args()
+
+    configs_search_str = os.path.join(args.workspace, "**", "metagenome_*.config")
+    config_fpaths = glob(configs_search_str, recursive=True)
+    for config_fpath in config_fpaths:
+        mgargs = config.parse_config(config_fpath)
+        ncbi = NCBI(dirpath=mgargs.databases.ncbi)
+        annotations = merge_annotations(mgargs)
+        for domain, bin_df in annotations.items():
+            if bin_df.empty:
+                logger.info(f"{domain} bin_df empty, skipping...")
+                continue
+
+            if args.write:
+                logger.info(f"Writing {domain} MetaBins")
+                domain_outdir = os.path.join(
+                    mgargs.parameters.outdir, "metabins", domain
+                )
+                write_cluster_records(
+                    bin_df=bin_df,
+                    metagenome=mgargs.files.metagenome,
+                    outdir=domain_outdir,
+                )
+            logger.info(f"Retrieving {domain} MetaBins' stats")
+            markers_fpath = (
+                mgargs.files.bacteria_markers
+                if domain == "bacteria"
+                else mgargs.files.archaea_markers
+            )
+            df = get_metabin_stats(
+                bin_df=bin_df,
+                markers_fpath=markers_fpath,
+                assembly=mgargs.files.metagenome,
+            )
+            if os.path.exists(mgargs.files.taxonomy) and os.path.getsize(
+                mgargs.files.taxonomy
+            ):
+                logger.info(f"Retrieving {domain} MetaBins' taxonomies")
+                taxa_df = get_metabin_taxonomies(bin_df=bin_df, ncbi=ncbi)
+                df = pd.merge(
+                    df, taxa_df, how="left", left_index=True, right_index=True
+                )
+            if args.write:
+                outfpath = os.path.join(
+                    mgargs.parameters.outdir,
+                    "metabins",
+                    f"{domain}_metabin_summary.tsv",
+                )
+            else:
+                outfpath = os.path.join(
+                    mgargs.parameters.outdir, f"{domain}_metabin_summary.tsv"
+                )
+
+            df = df.convert_dtypes()
+            df.to_csv(outfpath, sep="\t", index=True, header=True)
+
+
+if __name__ == "__main__":
+    main()