Many thanks. I will have a try.
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I genotyped a sample by Illumina SNP array and I sequenced its exome sequencing data. What is the sensitivity of genotype calling from sequencing data? Is there already perl script?
You might want to look at these two tools:
http://vcftools.sourceforge.net/perl_module.html#vcf-compare
http://www.broadinstitute.org/gsa/wiki/index.php/VariantEval
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So which one is more accurate - genotyping or sequencing?