-- Now you always get SNP and indel metrics with VariantEval!
-- Includes Number of SNPs, Number of singleton SNPs, Number of Indels, Number of singleton Indels, Percent of indel sites that are multi-allelic, SNP to indel ratio, Singleton SNP to indel ratio, Indel novelty rate, 1 to 2 bp indel ratio, 1 to 3 bp indel ratio, 2 to 3 bp indel ratio, 1 and 2 to 3 bp indel ratio, Frameshift percent, Insertion to deletion ratio, Insertion to deletion ratio for 1 bp events, Number of indels in protein-coding regions labeled as frameshift, Number of indels in protein-coding regions not labeled as frameshift, Het to hom ratio for SNPs, Het to hom ratio for indels, a Histogram of indel lengths, Number of large (>10 bp) deletions, Number of large (>10 bp) insertions, Ratio of large (>10 bp) insertions to deletions
-- Updated VE integration tests as appropriate
-- Moved a variety of useful formatting routines for ratios, percentages, etc, into VariantEvalator.java so everyone can share. Code updated to use these routines where appropriate
-- Added variantWasSingleton() to VariantEvaluator, which can be used to determine if a site, even after subsetting to specific samples, was a singleton in the original full VCF
-- TableType, which used to be an interface, is now an abstract class, allowing us to implement some generally functionality and avoid duplication.
-- This included creating a getRowName() function that used to be hardcoded as "row" but how can be overridden.
-- #### This allows us implement molten tables, which are vastly easier to use than multi-row data sets. See IndelHistogram class (in later commit) for example of molten VE output
-- No more IndelLengthHistogram (superceded by IndelSummary in subsequent commit)
-- No more SamplePreviousGenotypes or PhaseStats
-- No more MultiallelicAFs
-- instead of using y = rbind(x, y), which is O(n^2) in a loop when processing lines into a data structure in R, preallocate a matrix and explicitly assign each row to x. This results in a radical performance improvement when reading large tables into R. It's possible with this optimization to read in a 70MB table for variantQCReport.R with 200K lines for 800 samples.
* fixed BadCigarFilter to filter out reads starting/ending in deletion and that have adjacent I/D events.
* added Unit tests for BadCigarFilter
* updated all exceptions in LocusIteratorByState to tell the user that he can instead run with -rf BadCigar
* added the BadCigar filter to ReduceReads and RealignTargetCreator (if your walker blows up with these malformed reads, you may want to add it too)
- Updated the documentation on the code
- Made the table.write() method private and updated necessary files.
- Added a constructor to GATKReport that takes GATKReportTables
- Optimized my code
Signed-off-by: Mauricio Carneiro <carneiro@broadinstitute.org>
This is important for quick turnaround in the analysis cycle of the new covariates. Also added a dummy unit test that doesn't really test anything (disabled), but helps in debugging.
Mark DePristo
Menachem Fromer
Guillermo del Angel
Eric Banks
Ryan Poplin
Mauricio Carneiro
Khalid Shakir
Roger Zurawicki