Thanks Ashutosh, tabix will do exactly what I'm looking for.
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Hi all,
Could anyone suggest how to extract variability within a range, i.e. candidate regions, from multiple vcf files?
I have exome data from a number of samples, as well as SNP array data, and I'm looking for recessive variability from the exome data within generated runs of homozygosity.
Thanks for your time
Tabix can help you if you are looking for variants in a given genomic region (http://samtools.sourceforge.net/tabix.shtml)
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