DE_analysis params change input types to numeric
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@ -175,7 +175,7 @@ docker-run:
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--ref_genome differential_expression_mouse/GRCm39.genome.fa.gz \
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--ref_annotation differential_expression_mouse/gencode.vM33.annotation.gtf \
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--direct_rna --ref_transcriptome differential_expression_mouse/gencode.vM33.transcripts.fa.gz \
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--transcriptome_assembly false --sample_sheet test_data/sample_sheet.csv \
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--transcriptome_assembly false --sample_sheet differential_expression_mouse/sample_sheet.csv \
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-c demo.nextflow.config"
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NF_IGNORE_PROCESSES: >
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preprocess_reads,merge_transcriptomes,assemble_transcripts,decompress_annotation,
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@ -4,6 +4,11 @@ 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/1.1.0/),
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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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### Fixed
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- Differential expression failing with 10 or more samples.
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- Regression causing the DE analysis numeric parameters to not be evaluated correctly.
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## [v1.1.0]
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### Changed
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- Improve documentation around filtering of transcripts done before DTU analysis.
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@ -5,10 +5,10 @@ suppressMessages(library("GenomicFeatures"))
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suppressMessages(library("edgeR"))
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args <- commandArgs(trailingOnly=TRUE)
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ref_annotation <- args[1]
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min_samps_gene_expr <- args[2]
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min_samps_feature_expr <- args[3]
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min_gene_expr <- args[4]
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min_feature_expr <- args[5]
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min_samps_gene_expr <- as.numeric(args[2])
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min_samps_feature_expr <- as.numeric(args[3])
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min_gene_expr <- as.numeric(args[4])
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min_feature_expr <- as.numeric(args[5])
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annotation_type <- args[6]
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strip_version <- args[7]
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