T2T-CHM13 improves read mapping and detection of clinically relevant genetic variation in the Swedish population

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Figure 7.
Figure 7.

Summaries of several per-individual variant call statistics. Statistics included only variants passing filters. (A) Number of overall variants. (B) Number of SNVs and indels. (C) Fraction of SNVs and indels of called variants. (D) Number of singletons. (E) Number of LoF variants.

This Article

  1. Published in Advance September 16, 2025, doi: 10.1101/gr.279320.124 Genome Res. 35: 2377-2388

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