-- Now the only use for update0, calculating the number of processed loci, is centrally tracked in the walker itself not the evaluations.
-- This allows us to avoid calling update0 are every genomic base in 100ks of evaluates when there are a lot of stratifications.
-- No need to modify the integration tests, this optimization doesn't change the result of the calculation
* added empirical quality counts to allow quantization during on-the-fly recalibration to any level
* added number of observations and errors to all tables to enable plotting of all covariates
* restructured BQSR to report recalibrated tables.
* implemented empirical quality calculation to the BQSR stage (instead of on-the-fly recalibration)
* linked quality score quantization to the BQSR stage, outputting a quantization histogram
* included the arguments used in BQSR to the GATK Report
* included all three tables (RG, QUAL and COVARIATES) to the GATK Report with empirical qualities
On-the-fly recalibration with GATK Report
* loads all tables from the GATKReport using existing infrastructure (with minor updates)
* implemented initialiazation of the covariates using BQSR's argument list
* reduced memory usage significantly by loading only the empirical quality and estimated quality reported for each bit set key
* applied quality quantization to the base recalibration
* excluded low quality bases from on-the-fly recalibration for mismatches, insertions or deletions
-- Still need to deal with the need to have a gold-standard track that isn't a stratification but is actually just provided as is for use to eval modules. This is currently stopping us from computing the % gold standard calls discovered, and the % of gold standard calls in the call set.
-- This behavior, which isn't obviously valuable at all, continued to grab and rethrow exceptions in the HMS that, if run without NT, would show up as more meaningful errors. Now HMS simply checks whether the throwable it received on error was a RuntimeException. If so, it is stored and rethrow without wrapping later. If it isn't, only in this case is the exception wrapped in a ReviewedStingException.
-- Added a QC walker ErrorThrowingWalker that will throw a UserException, ReviewedStingException, and NullPointerException from map as specified on the command line
-- Added IT that ensures that all three types are thrown properly (i.e., you catch a NullPointerException when you ask for one to be thrown) with and without threading enabled.
-- I believe this will finally put to rest all of these annoying HMS captures.
-- Use a LinkedHashMap not a TreeMap so iteration is faster.
-- Note that with a lot of stratifications the update0 is taking up a lot of time. For example, with 822 samples and functional class and sample on there are 100K contexts and 30% of the runtime is just in the update0 call
-- All new IndelSummary features used by default with variantCallQC.R script with PostCallingQC.scala
-- This includes many new per sample and per AC indel QC metrics.
-- Better plotting style throughout, with nice histograms, white backgrounds, etc
-- PostCallingQC is super easy to use now, just give it --evalvcfs and go. Tell it to run with 8 threads to finish quick. It's really easy and produces beautiful new figures (will replace with one attached)
-- 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)