Thousands of human mutation clusters are explained by short-range template switching

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Figure 7.
Figure 7.

Complex gnomAD MNV explained by a single TSM. (A) Wang et al. (2020) identified 15 SNVs within a 29-bp interval in Chromosome 12. (B) All the differences (top, marked with asterisks) can be explained with a TSM inverting a 39-bp-long fragment in place (middle, bottom).

This Article

  1. Published in Advance June 27, 2022, doi: 10.1101/gr.276478.121 Genome Res. 32: 1437-1447

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