USeq Source Code

Brought to you by: biotelerock, bmilash, elainegee, scourdy, tmosbruger

Source Code Commit Log

Commit	Date
[r200] by biotelerock Added indel support to the VCFSpliceAnnotator	2013-12-30 22:08:30	Tree
[r199] by biotelerock * Added a catch to skip calculating stats on bins with only one value * Fixed bug with the ordering of the bins in the ggplot	2013-12-23 17:22:25	Tree
[r198] by biotelerock Added new SamSVFilter app to build	2013-12-20 17:21:53	Tree
[r197] by biotelerock	2013-12-20 17:19:48	Tree
[r196] by biotelerock Backed out Darrens changes until these are optional	2013-12-20 17:16:28	Tree
[r195] by tmosbruger	2013-12-18 00:00:59	Tree
[r194] by tmosbruger MultiSampleVCFFilter: Bug fix, the behavior of -M was incorrect.	2013-12-16 17:32:59	Tree
[r193] by monkeymanstan Added code to call Picard's SortSam and MarkDuplicates at start of NBP	2013-12-16 16:22:36	Tree
[r192] by tmosbruger VCFSample: Mark samples with no depth information as no-calls	2013-12-11 18:45:14	Tree
[r191] by biotelerock DefinedRegionDifferentialSeq * Changed the default minimum read count threshold to 20 from 10. This lower number was allowing too many low hit genes into the multiple testing correct and causing the FDRs to be significantly lower than necessary. VCFComparator * Added checks to convert 0\|1 genotypes to 0/1, and 1/0 calls to 0/1; these are needed to standardize the calls and enable genotype matching with the NIST key SamTranscriptomeParser * Bug fix for merging paired alignments where an insertion occurred immediately before the start of the second read	2013-12-10 22:50:48	Tree

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