wf-transcriptomes-v202/CHANGELOG.md

1.5 KiB

Changelog

All notable changes to this project will be documented in this file.

The format is based on Keep a Changelog, and this project adheres to Semantic Versioning.

[unreleased]

Updated

  • Removed sanitize option

Added

  • Demo differential expression data in repository.
  • Improved DE explanation in docs

Fixed

  • Error if condition sheet and sample sheet don't match.

[v0.1.5]

Added

  • Differential transcript and gene expression subworkflow

[v0.1.4]

Added

  • JAFFAL fusion detection subworkflow

Changed

  • Args parser for fastqingress
  • Set out_dir option type to ensure output is written to correct directory on Windows
  • Skip unnecessary conversion to fasta from fastq
  • Fastqingress metadata map
  • Changed workflow name to wf-transcriptomes

[v0.1.3]

Changed

  • Better help text on cli
  • Use EPI2ME Labs-maintained version of pychopper

[v0.1.2]

Added

  • direct_rna option
  • Some extra error handling
  • Minor report display improvements

[v0.1.1]

Fixed

  • Incorrect numbers and of transcripts caused by merging gff files with same gene and transcript ids
  • Error handling in de novo pipeline. Skip clusters in build_backbones that cause an isONclust2 error
  • Several small fixes in report plotting

[v0.1.0]

Added

  • Added the denovo pipeline

Changed

  • Updates to the report plots

[v0.0.1]

Added