Variant Detection Statistics for Pooled Sequencing.
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The number in parentheses represents only variants at 5% or lower frequency in the dataset.1- Statistics for variant sites which were sequenced to a depth of 10 or 30 fold per individual in the pooled dataset.2- Variants called in the pooled dataset not present in either HapMap or the 1000 Genome Project. Variants were further classified as being included or absent in dbSNP v130.3- Variants called in the HapMap or 1000 Genome Project that were not called in our pooled dataset.
创建时间：
2015-12-02
