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CNV
BCF2 with support symbolic alleles
2012-06-30 11:22:48 -04:00
annotator
Update MD5s with new FS score
2012-08-28 08:06:47 -04:00
beagle
Fixing remaining integration test errors. Adding missing ex2.bcf
2012-06-30 16:23:11 -04:00
bqsr
Bad news folks: BQSR scatter-gather was totally busted; you absolutely cannot trust any BQSR table that was a product of SG (for any version of BQSR). I fixed BQSR-gathering, rewrote (and enabled) the unit test, and confirmed that outputs are now identical whether or not SG is used to create the table.
2012-09-20 14:14:34 -04:00
coverage
number of stashed changes are lurking in here. In order of importance:
2012-08-21 07:08:58 -04:00
diagnostics
Fixing remaining integration test errors. Adding missing ex2.bcf
2012-06-30 16:23:11 -04:00
diffengine
Cleanup of VCF header lines and constants, BCF2 bugfixes
2012-06-21 15:16:31 -04:00
fasta
Several more walkers have been brought up to use the new Allele representation.
2012-07-27 02:14:25 -04:00
filters
Integration test to ensure VariantFiltration makes . -> PASS/FAIL like VQSR
2012-07-25 08:56:39 -04:00
genotyper
Updating MD5s for confidence ref site estimation in IndependentAllelesDiploidExactAFCalc
2012-10-23 06:47:53 -04:00
indels
Allowing the GATK to have non-required outputs
2012-10-15 13:49:08 -04:00
phasing
- Multi-allelic sites are now correctly ignored - Reporting of mendelian violations enhanced - Corrected TP overflow by caping it to Bye.MAX_VALUE
2012-07-17 15:21:10 -04:00
qc
First version of VariantContextBuilder
2011-11-18 11:06:15 -05:00
validation
Allele refactoring checkpoint #3 : all integration tests except for PoolCaller are passing now. Fixed a couple of bugs from old code that popped up during md5 difference review. Added VariantContextUtils.requiresPaddingBase() method for tools that create alleles to use for determining whether or not to add the ref padding base. One of the HaplotypeCaller tests wasn't passing because of RankSumTest differences, so I added a TODO for Ryan to look into this.
2012-07-27 15:48:40 -04:00
varianteval
In AlleleCount stratification, check to make sure the AC (or MLEAC) is valid (i.e. not higher than number of chromosomes) and throw a User Error if it isn't. Added a test for bad AC.
2012-08-14 15:02:30 -04:00
variantrecalibration
Update md5s for VQSR, as VQSLOD is now a double and gets the standard double precision treatment in VCF
2012-08-30 19:41:49 -04:00
variantutils
Updating integration tests for minor changes due to switching to EXACT_INDEPENDENT model by default
2012-10-21 12:43:46 -04:00
BAQIntegrationTest.java
merge master
2011-10-25 16:08:39 -04:00
ClipReadsWalkersIntegrationTest.java
Cleanup of VCF header lines and constants, BCF2 bugfixes
2012-06-21 15:16:31 -04:00
FlagStatIntegrationTest.java
Adding integration test for Flag Stat
2012-04-10 22:40:38 -04:00
PileupWalkerIntegrationTest.java
Done GSA-282: Unindexed traversals crash if a read goes off the end of a contig
2012-09-05 21:10:03 -04:00
PrintReadsIntegrationTest.java
ReadShard are no longer allowed to span multiple contigs
2012-08-30 10:15:11 -04:00
PrintReadsUnitTest.java
Removed the "Walker" suffix from all walkers that had it.
2012-07-20 17:27:11 -04:00