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Coverage required for Sanger based SNP detection and Genotyping
Does anyone know of an established acceptable figure in terms of times coverage required for SNP/calling and genotyping with Sanger sequences?
I know 20x is generally recommended for NGS but this is obviously a different scenario. |
many papers using the Sanger sequences ,but didn't give a criteria . maybe 10x is enough.
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We take 2x coverage for SNP calling in our lab.
Ventner's genome was done to 7.5x (http://www.nature.com/nrg/journal/v1...df/nrg2626.pdf) Cheers Paul |
Did you get a good result ? what's FP and FN ?
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