Skip to content

v1.1

Latest
Compare
Choose a tag to compare
@mfoll mfoll released this 23 May 07:21
· 2 commits to master since this release
9d8d7b8

Full Changelog

Implemented enhancements:

  • add needlestack logo in log.info #182
  • add INFO field containing allelic frequency #174
  • Add an option to only plot somatic mutations #149
  • Make the main 3 processes pipe-friendly to avoid intermediate outputs #147
  • Re-write pileup2baseindel.pl in C++ #146
  • Flag possible cross-sample contamination of normal DNA in tumor samples #138
  • Put ./. genotype when there is no power to identify a variant #137
  • Implement Tumor-Normal pair somatic variant calling #133
  • Add alignment plot in the PDF #73
  • Make a script that would run needlestack without nextflow #72

Fixed bugs:

  • max_dp default value in readme is wrong #176
  • --help should exit 0 #161
  • Manage bed specification for both bed and region #157
  • Using renamed symlinks as input BAM files doesn't work with --use_file_name option #152

Closed issues:

  • How to identify each sample? #166
  • Github readme != Docker readme #159