recent changes
Browse files- .gitignore +5 -1
- dpacman/data/consistency.py +10 -0
- dpacman/data/remap/analyze.py +2 -0
- dpacman/data/tfclust/combine.py +64 -4
.gitignore
CHANGED
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@@ -4,4 +4,8 @@ dpacman/data/tfclust/temp.py
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bigBedToBed
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dpacman/data/remap/*.log
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dpacman/data/remap/temp.py
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dpacman/data/tfclust/figures
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bigBedToBed
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dpacman/data/remap/*.log
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dpacman/data/remap/temp.py
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dpacman/data/tfclust/figures
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dpacman/softwares
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dpacman/data/remap/crm_example.csv
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dpacman/data/remap/crm_example_ERG.csv
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tree.txt
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dpacman/data/consistency.py
ADDED
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@@ -0,0 +1,10 @@
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"""
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Check for consistency between Remap and Tfclust data
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"""
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import logging
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import pandas as pd
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import logging
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import os
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import dask.dataframe as dd
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dpacman/data/remap/analyze.py
CHANGED
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@@ -10,6 +10,8 @@ def main(logger=None):
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df = pd.read_csv(bed_file_path, sep="\t", header=None)
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df.columns = ["#chrom", "chromStart", "chromEnd", "name", "score", "strand", "thickStart", "thickEnd", "reserved", "TF", "Biotypes"]
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print(f"{len(df):,}")
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print(df.head(50))
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crm_bed_file_path = "../../data_files/raw/remap/remap2022_crm_macs2_hg38_v1_0.bed"
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df = pd.read_csv(bed_file_path, sep="\t", header=None)
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df.columns = ["#chrom", "chromStart", "chromEnd", "name", "score", "strand", "thickStart", "thickEnd", "reserved", "TF", "Biotypes"]
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print(f"{len(df):,}")
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crm["chromLen"] = crm["chromEnd"] - crm["chromStart"]
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print(crm["chromLen"].describe())
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print(df.head(50))
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crm_bed_file_path = "../../data_files/raw/remap/remap2022_crm_macs2_hg38_v1_0.bed"
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dpacman/data/tfclust/combine.py
CHANGED
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@@ -3,10 +3,7 @@ import logging
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import os
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import dask.dataframe as dd
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def
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hg38_dir = "../../data_files/processed/tfclust/hg38"
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hg19_dir = "../../data_files/processed/tfclust/hg19"
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# See how many files there are
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hg38_files = [os.path.join(hg38_dir,x) for x in os.listdir(hg38_dir) if os.path.isfile(os.path.join(hg38_dir,x))]
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hg19_files = [os.path.join(hg19_dir,x) for x in os.listdir(hg19_dir) if os.path.isfile(os.path.join(hg19_dir,x))]
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@@ -46,7 +43,70 @@ def main():
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os.makedirs(full_df_dir, exist_ok=True)
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full_df.to_parquet(full_df_savepath) # much faster and more compact
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logging.info(f"Saved combined DataFrame to {full_df_savepath}.")
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if __name__ == "__main__":
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logging.basicConfig(filename="combine.log", encoding="utf-8", level=logging.DEBUG, filemode="w")
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import os
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import dask.dataframe as dd
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def combine_hg38_hg19(hg38_dir, hg19_dir):
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# See how many files there are
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hg38_files = [os.path.join(hg38_dir,x) for x in os.listdir(hg38_dir) if os.path.isfile(os.path.join(hg38_dir,x))]
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hg19_files = [os.path.join(hg19_dir,x) for x in os.listdir(hg19_dir) if os.path.isfile(os.path.join(hg19_dir,x))]
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os.makedirs(full_df_dir, exist_ok=True)
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full_df.to_parquet(full_df_savepath) # much faster and more compact
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logging.info(f"Saved combined DataFrame to {full_df_savepath}.")
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# Define the aggregation function
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def collapse_group(group):
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return pd.Series({
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"name": ",".join(group["name"]),
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"score": ",".join(map(str, group["score"])),
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"bin": ",".join(map(str, group["bin"])),
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"scoreCount": ",".join(map(str, group["scoreCount"])),
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"sourceIds": ",".join(map(str, group["sourceIds"])),
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"sourceScores": ",".join(map(str, group["sourceScores"])),
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})
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def reorg_like_remap(genome_dir, fname):
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"""
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Reorganize a chromosome from tfclust processing to be in the format of remap files:
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#chrom,chromStart,chromEnd,name,score,strand,thickStart,thickEnd,reserved,chromLen,thickLen
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Original format of my processed tfclust files
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bin,chrom,chromStart,chromEnd,name,score,scoreCount,sourceIds,sourceScores,seq,seq_flanked,chromStart_flanked,chromEnd_flanked,flank5,flank3
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"""
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fpath = os.path.join(genome_dir, fname)
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df = dd.read_csv(fpath)
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# Show the head
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print(df.head())
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# Keep everything except the sequences
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df = df[[
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"chrom", "chromStart", "chromEnd", "name", "score", # same as other file
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"bin","scoreCount","sourceIds","sourceScores"
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]].rename(columns={"chrom":"#chrom"})
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# Apply groupby with known output types (meta)
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meta = {
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"name": str,
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"score": str,
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"bin": str,
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"scoreCount": str,
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"sourceIds": str,
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"sourceScores": str
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}
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grouped = df.groupby(["#chrom", "chromStart", "chromEnd"]).apply(collapse_group, meta=meta)
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# You can now compute it
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result = grouped.compute()
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# save the result
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savepath = os.path.join(genome_dir, "remap_reorg")
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os.makedirs(savepath, exist_ok=True)
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savepath = os.path.join(savepath, fname.replace(".csv", "_reorg.csv"))
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result.to_csv(os.path.join(genome_dir), index=True)
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logging.info(f"Saved reorganized file to {savepath}")
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def main():
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hg38_dir = "../../data_files/processed/tfclust/hg38"
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hg19_dir = "../../data_files/processed/tfclust/hg19"
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#combine_hg38_hg19(hg38_dir, hg19_dir)
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for chrom in ["chr1"]:
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reorg_like_remap(hg38_dir, f"encRegTfbsClustered_hg38_{chrom}.csv")
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if __name__ == "__main__":
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logging.basicConfig(filename="combine.log", encoding="utf-8", level=logging.DEBUG, filemode="w")
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