Next-generation sequencing (NGS) is a key technology in understanding the causes and consequences of human genetic variability. In this context, the validity of NGSinferred single-nucleotide variants (SNVs) is of paramount importance. We therefore developed a statistical framework to assess the fide
The Fourth Annual Meeting of the International Genetic Epidemiology Society, June 20–22, 1995, Snowbird, Utah
✍ Scribed by Melissa A. Austin
- Publisher
- John Wiley and Sons
- Year
- 1996
- Tongue
- English
- Weight
- 244 KB
- Volume
- 13
- Category
- Article
- ISSN
- 0741-0395
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