Commit | Date | |
---|---|---|
[r297]
by
biotelerock
Sam2USeq: Fixed an issue where chromData from the MergePairedAlignments app fail to calc read coverage with b37 no "chr" data. Now must match the bed file with the alignments. PoReCNV: change the way loaded data is saved to enable per sample loading for additional runs. VCF mods to support parsing of LoFreq's crazy vcf format New app for converting a bed file to a gene table by intersecting it with another gene table. |
2015-06-06 14:29:23 | Tree |
[r296]
by
biotelerock
OK: |
2015-05-27 17:04:00 | Tree |
[r295]
by
dnephi
Made a number of changes as I'm writing the read pair flattener for barcoded reads. |
2015-05-15 23:00:56 | Tree |
[r294]
by
tmosbruger
Read lengths are calculated using the reported sequence vs perfect cigar. This avoids crashes when there are very few reads. |
2015-04-21 23:12:12 | Tree |
[r293]
by
biotelerock
Added functionality to PoReCNV to join adjacent passing exons into larger CNV block. |
2015-04-15 21:38:06 | Tree |
[r292]
by
biotelerock
Fixed an issue with PoReCNV where the last chromosome of data wasn't being processed when batching R calls. |
2015-04-03 15:23:29 | Tree |
2015-04-01 17:06:11 | Tree | |
[r290]
by
tmosbruger
Sam2USeq: Prepend chr to bed regions, if it isn't there already. |
2015-04-01 14:30:26 | Tree |
[r289]
by
biotelerock
Dropped support for unsorted sam.gz files, this was causing issues with files that had no phiX |
2015-03-17 20:20:17 | Tree |
[r288]
by
biotelerock
Lots of mods to the individual VCF parsers to standardize them for merging with Somatic variant analysis. More mods to the PoReCNV app. Fixed an issue with the CollectBamStats where changes to the default thresholds were being overwritten. |
2015-03-17 16:55:08 | Tree |