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Variant Detection Statistics for Pooled Sequencing.

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https://figshare.com/articles/dataset/_Variant_Detection_Statistics_for_Pooled_Sequencing_/458665
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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.
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2011-03-30
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