Postmortem genetic screening for the identification, verification, and reporting of genetic variants contributing to the sudden death of the young

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Figure 2.
Figure 2.

Workflow of genetic variant screening. All quality annotated SNVs and indel variants were filtered in order to classify variants as pathogenic in SD.

This Article

  1. Published in Advance July 19, 2016, doi: 10.1101/gr.195800.115 Genome Res. 26: 1170-1177

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