Re-identification of human genome variations from the 1000 Genomes pilot project.
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SNP: Single Nucleotide Variant SV: Structural Variation.1Re-identified by TASR. Only reads spanning variation within 5 bases of read start/end were counted.2In superscript, genotypes were determined by the 1000 genomes project. This information is not available for SVs.3A/B : A = coverage of reads over the non-deleted portion B = coverage over the deletion breakpoint.4x = ACTAGTGCATTTCAATAATCATG.Underlined are discrepancies between TASR and the genotype calls, all of which are due to insufficient read coverage.
创建时间：
2015-12-02
