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Published April 15, 2025 | Version v1.7.0

epi2me-labs/wf-transcriptomes: v1.7.0

  • 1. @Birkbeck
  • 2. Oxford Nanopore Technologies
  • 3. @nanoporetech
  • 4. @nanoporetech, @epi2me-labs

Description

Changed

  • split_bam and build_minimap_index_transcriptome process memory allocation increased.
  • Updated recommended memory requirement.
  • Updated project description.
  • A common user issue is providing a ref_annotation and ref_genome parameter that have mismatched reference IDs, which causes the DE_analysis to fail. The workflow will now do an upfront check and give an error message if no overlap is found or a warning if some IDs are present in one file but not in the other.
  • Reconciled workflow with wf-template v5.5.0.
  • Sort the columns and rows of the gene and transcript count files.
  • DE_analysis alignment summary stats table no longer includes MAPQ or quality scores. MAPQ is not relevant for transcript alignment and quality scores are already available in the read summary section of the report.

Fixed

  • all_gene_counts.tsv contained the DE counts results.
  • Reduced memory usage of the report workflow process.
  • Output BAM alignments in all cases unless the workflow is run with transcriptome_source set to precomputed.
  • Corrected the demo command in the README.md.
  • The merged transcriptome generated for differential expression analysis now only contains the exons and not the full genomic sequence.
  • Output the gene name annotated differential expression analysis count files only.
  • Only use full length reads in the differential expression analysis.

Files

epi2me-labs/wf-transcriptomes-v1.7.0.zip

Files (124.4 MB)

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Additional details

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