Hi, I would like to display "Variant Call Format"(http://vcftools.sourceforge.net/specs.html) data in the UCSC Genome Browser, I would like to use "Personal Genome SNP Format", should I write a parser for that or is this something someone else have done before?.
And also, is there any variant calling software out there outputting directly to pgSNP format or at least to a format easy to migrate to pgSNP? Thanks, -- Carlos Borroto Baltimore, MD _______________________________________________ Genome maillist - [email protected] https://lists.soe.ucsc.edu/mailman/listinfo/genome
