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

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Figure 5.
Figure 5.

Number of genes with predicted LoF variants shared among assemblies.

This Article

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

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