Identified SNVs by MutAid pipeline.
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资源简介：
SNVs were called using four variant callers (for each mapping result) with a minimum read coverage of 20, minimum variant allele coverage of 4 and a base quality of at least 20. The percentage given in brackets is the fraction of SNVs having an entry in the Single Nucleotide Polymorphism Database (dbSNP) version 137.
创建时间：
2016-02-03
