CW-1170 Fix failed to plot
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@ -4,7 +4,7 @@ All notable changes to this project will be documented in this file.
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The format is based on [Keep a Changelog](https://keepachangelog.com/en/1.0.0/),
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and this project adheres to [Semantic Versioning](https://semver.org/spec/v2.0.0.html).
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## [unreleased]
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## [v0.1.6]
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### Updated
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- Removed sanitize option
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- Reduce size of differential expression data.
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@ -14,6 +14,8 @@ and this project adheres to [Semantic Versioning](https://semver.org/spec/v2.0.0
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### Fixed
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- Fix JAFFAL terminating workflow when no fusions found.
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- Error if condition sheet and sample sheet don't match.
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- Failed to plot DE graphs when one of data sets is 0 length.
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## [v0.1.5]
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### Added
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@ -205,9 +205,9 @@ thresholds defined are shaded as 'Up-' or 'Down-' regulated.""")
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],
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title="Average copy per million (CPM) vs Log-fold change (LFC)",
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colors=["red", "blue", "black"],
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xlim=[0, 5],
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names=["Up", "Down", "NotSig"]
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)
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dexseq_plot.xaxis.axis_label = "A (log2 transformed mean exon read counts)"
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dexseq_plot.yaxis.axis_label = """
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M (log2 transformed differential abundance)
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@ -277,10 +277,9 @@ defined are shaded as 'Up-' or 'Down-' regulated.
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not_sig["logFC"],
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],
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title="Average copy per million (CPM) vs Log-fold change (LFC)",
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colors=["blue", "red", "black"],
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colors=["red", "blue", "black"],
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names=["Up", "Down", "NotSig"]
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)
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logcpm_vs_logfc.xaxis.axis_label = "Average log CPM"
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logcpm_vs_logfc.yaxis.axis_label = "Log-fold change"
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logcpm_caption = """### Results of the edgeR Analysis."""
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@ -11,35 +11,35 @@ import pandas as pd
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parser = argparse.ArgumentParser(
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description="""Merge tab separated files on a given field using pandas.""")
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parser.add_argument(
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'-j', metavar='join', type=str, help="Join type (outer).", default="outer")
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'-j', metavar='join', help="Join type (outer).", default="outer")
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parser.add_argument(
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'-f', metavar='field', type=str,
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'-f', metavar='field',
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help="Join on this field (Reference).", default="Reference")
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parser.add_argument(
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'-o', metavar='out_tsv', type=str,
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'-o', metavar='out_tsv',
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help="Output tsv (merge_tsvs.tsv).", default="merge_tsvs.tsv")
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parser.add_argument(
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'-z', action="store_true",
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help="Fill NA values with zero.", default=False)
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parser.add_argument(
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'tsvs', metavar='input_tsvs', nargs='*',
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type=str, help="Input tab separated files.")
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parser.add_argument(
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'-tpm', type=bool, nargs='*', default=False,
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'-tpm', type=bool, default=False,
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help="TPM instead of counts")
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parser.add_argument(
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'-tsvs', metavar='input_tsvs', nargs='*',
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help="Input tab separated files.")
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if __name__ == '__main__':
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args = parser.parse_args()
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args = parser.parse_args()
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dfs = {x: pd.read_csv(x, sep="\t") for x in args.tsvs}
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ndfs = []
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for x, df in dfs.items():
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# Transform counts to integers:
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df = df.rename(columns={'NumReads': 'Count', 'Name': 'Reference'})
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if args.tpm:
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df = df.rename(columns={'TPM': 'Count', 'Name': 'Reference'})
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else:
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df = df.rename(columns={'NumReads': 'Count', 'Name': 'Reference'})
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df.Count = np.array(df.Count, dtype=int)
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# Take only non-zero counts:
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df = df[df.Count > 0]
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@ -7,7 +7,7 @@ channels:
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dependencies:
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- python==3.8.*
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- bokeh==2.4.3
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- aplanat>=0.6.4
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- aplanat>=0.6.15
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- epi2melabs
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- minimap2==2.24
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- samtools==1.14
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@ -23,7 +23,7 @@ params {
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out_dir = "output"
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sample = null
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sample_sheet = null
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wfversion = "v0.1.5"
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wfversion = "v0.1.6"
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aws_image_prefix = null
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aws_queue = null
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report_name = "report"
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@ -363,7 +363,7 @@
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},
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"wfversion": {
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"type": "string",
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"default": "v0.1.5",
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"default": "v0.1.6",
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"hidden": true
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},
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"monochrome_logs": {
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@ -2,6 +2,7 @@ process count_transcripts {
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// Count transcripts using Salmon.
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// library type is specified as forward stranded (-l SF) as it should have either been through pychopper or come from direct RNA reads.
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label "isoforms"
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cpus params.threads
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input:
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tuple val(sample_id), path(bam)
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path ref_transcriptome
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@ -9,9 +10,9 @@ process count_transcripts {
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path "*transcript_counts.tsv", emit: counts
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path "*seqkit.stats", emit: seqkit_stats
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"""
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salmon quant --noErrorModel -p $params.threads -t $ref_transcriptome -l SF -a $bam -o counts
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mv counts/quant.sf "${sample_id}".transcript_counts.tsv
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seqkit bam "$bam" 2> "${sample_id}".seqkit.stats
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salmon quant --noErrorModel -p "${task.cpus}" -t "${ref_transcriptome}" -l SF -a "${bam}" -o counts
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mv counts/quant.sf "${sample_id}.transcript_counts.tsv"
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seqkit bam "${bam}" 2> "${sample_id}.seqkit.stats"
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"""
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}
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@ -23,7 +24,7 @@ process mergeCounts {
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output:
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path "all_counts.tsv"
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"""
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merge_count_tsvs.py -z -o all_counts.tsv $counts
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merge_count_tsvs.py -z -o all_counts.tsv -tsvs ${counts}
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"""
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}
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@ -34,7 +35,7 @@ process mergeTPM {
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output:
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path "tpm_counts.tsv"
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"""
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merge_count_tsvs.py -z -o tpm_counts.tsv $counts -tpm
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merge_count_tsvs.py -o tpm_counts.tsv -z -tpm True -tsvs $counts
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"""
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}
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@ -101,7 +102,7 @@ process build_minimap_index_transcriptome{
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path "genome_index.mmi", emit: index
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script:
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"""
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minimap2 -t ${params.threads} ${params.minimap_index_opts} -I 1000G -d "genome_index.mmi" ${reference}
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minimap2 -t "${task.cpus}" ${params.minimap_index_opts} -I 1000G -d "genome_index.mmi" "${reference}"
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"""
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}
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@ -123,10 +124,10 @@ process map_transcriptome{
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output:
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tuple val(sample_id), path("${sample_id}_reads_aln_sorted.bam"), emit: bam
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"""
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minimap2 -t ${params.threads} -ax splice -uf -p 1.0 $index $fastq_reads\
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| samtools view -Sb > output.bam
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samtools sort -@ ${params.threads} output.bam -o "${sample_id}"_reads_aln_sorted.bam
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samtools index "${sample_id}"_reads_aln_sorted.bam
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minimap2 -t ${task.cpus} -ax splice -uf -p 1.0 "${index}" "${fastq_reads}" \
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| samtools view -Sb > "output.bam"
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samtools sort -@ ${task.cpus} "output.bam" -o "${sample_id}_reads_aln_sorted.bam"
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samtools index "${sample_id}_reads_aln_sorted.bam"
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"""
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}
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