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Old 11-04-2011, 06:15 AM   #1
kjaja
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Location: NY

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Default variant calling

Are there tools out there that help in processing the variants calling output files from CASAVA? I have all the variant call files (SNPs and Indels) for all the individuals and I am looking into proceeding with analysis (case control study)

I appeciate your help
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Old 11-04-2011, 07:16 AM   #2
m_elena_bioinfo
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Hi! You can use a lot of different pipeline and tools for the variant calling. As free software, you can use samtools or GATK, games and annovar in the final step for the annotation of the identified variants
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