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. 2019 Jul 5;35(14):i242–i248. doi: 10.1093/bioinformatics/btz329

Table 2.

Phasing completeness and accuracy on whole-genome Strand-seq data for NA12878

Method SNVs phased (%) Switch error rate (%) Mismatch error rate (%) Absolute error rate (%)
Reads only 71.38 0.091 0.268 0.905
Integrated phasing 94.56 0.0364 0.134 0.868

Note: Results are shown for data on chromosome 20 only. Switch and mismatch error rates were calculated by comparison to Platinum Genomes haplotypes for NA12878.