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Old 11-29-2011, 07:15 AM   #1
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Location: uk

Join Date: Jan 2010
Posts: 110
Default Comparing and combining vcf files


I am trying to determine if there is an available solution for comparing vcf files and combining them into a single, non-redundant file?

So for example, if I have two vcf files for two patients, I would like to create one unique list of all the mutated locations observed in their genomes. Is there anything else out there or should I just script something?

Thanks in advance.
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