Low-coverage sequencing cost-effectively detects known and novel variation in underrepresented populations
Genetic studies in underrepresented populations identify disproportionate numbers of novel associations. However, most genetic studies use genotyping arrays and sequenced reference panels that best capture variation most common in European ancestry populations. To compare data generation strategies...
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Veröffentlicht in: | American journal of human genetics 2021-04, Vol.108 (4), p.656-668 |
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Sprache: | eng |
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