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CHANGELOG.md

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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.

[v0.0.9]

Fixed

  • VCF outputs are malformed if only one variant is called, this is now corrected

Changed

  • Increased maximum allowed total size of global variables in QDNAseq Rscript

Note

  • wf-cnv is now deprecated and will no longer receive updates, please use wf-human-variation

[v0.0.8]

Changed

  • --genome parameter no longer required (determined from reference or BAM)
  • Updated CI command to produce improved report
  • Report updated to use histogram function from ezcharts

[v0.0.7]

Added

  • Workflow can now take BAM as input, as well as FASTQ

Fixed

  • sample_sheet format in schema to expect a file

Changed

  • Documentation update

[v0.0.6]

Changed

  • Updated description in manifest
  • Documentation update

[v0.0.5]

Changed

  • Documentation update

[v0.0.4]

Fixed

  • --sample_sheet is now a path in the schema

Changed

  • --map_threads default is now 8 cores
  • Docs update

[v0.0.3]

Changed

  • QDNAseq R script no longer carries out separate female sample analysis

[v0.0.2]

Fixed

  • Prevented running with conda profile

Changed

  • Docs update
  • nextflow config fix
  • Increased memory from 8G -> 16G
  • CPU limit for alignment

[v0.0.1]

Added

  • CNV calling with QDNAseq