Hello, I have a several samples analyzed with 50K beadchip. I want to extract a subset of 100 SNPs based on quality parameter and MAF, equally distributed by cromosome. Please there is some istruction to do it in Plink? Regards
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Question: extract a SNPs set based on polimorfism in Plink
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landivincenzo • 0 wrote:
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modified 15 months ago
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Jennifer Hillman Jackson ♦ 25k
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15 months ago by
landivincenzo • 0
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Jennifer Hillman Jackson ♦ 25k wrote:
Hello,
The Plink tool wrapped for Galaxy could be installed and used in a local, docker or cloud Galaxy for most of the filtering.
First, filter per-chromosome/quality/maf with Plink. From there you can select how many SNPs from each per-chromosome filtered dataset to retain using the tool NGS: VCF Manipulation > VCFrandomSample or the tool Text Manipulation > Select random lines from a file (for the second, use a VCF without a header during line filtering, then add it back after if wanted). Merge the final results together using VCFcombine.
Hope this helps, Jen, Galaxy team
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