Resolving complex duplication variants in autism spectrum disorder using long-read genome sequencing

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Figure 1.
Figure 1.

Families selected for whole genome nanopore sequencing. Pedigrees of the families included in the study. Filled symbols indicate individuals diagnosed with ASD. Individuals selected for sequencing are denoted with an asterisk (*), and individuals previously shown to carry chromosomal rearrangements are marked with a hashtag (#).

This Article

  1. Published in Advance October 29, 2024, doi: 10.1101/gr.279263.124 Genome Res. 34: 1763-1773

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