Here is an example metrics output from a very tiny region:
Allele Frequency Metrics (LOD >= 5)
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Total loci : 14704
Total called with confidence : 10920 (74.27%)
Number of Variants : 16 (0.15%) (1/682)
Fraction of variant sites in dbSNP : 100.00%
Missing:
Microarray(hapmap) concordance, tp/fp.
Optional:
Histograms of depth of coverage, LOD, observed allele frequency, etc.
Still to implement:
Propagate command line argument N (number of chromosomes) into walker to enable pooled calling.
Take allele frequency priors as input.
git-svn-id: file:///humgen/gsa-scr1/gsa-engineering/svn_contents/trunk@133 348d0f76-0448-11de-a6fe-93d51630548a
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| core/java/src/org/broadinstitute/sting | ||
| doc | ||
| playground | ||
| settings | ||
| testdata | ||
| build.xml | ||
| ivy.xml | ||