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Anchored pseudo-de novo assembly of human genomes identifies extensive sequence variation from unmapped sequence reads
The human genome reference (HGR) completion marked the genomics era beginning, yet despite its utility universal application is limited by the small number of individuals used in its development. This is highlighted by the presence of high-quality sequence reads failing to map within the HGR. Sequen...
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| Yayımlandı: | Hum Genet |
|---|---|
| Asıl Yazarlar: | , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
2016
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4899208/ https://ncbi.nlm.nih.gov/pubmed/27061184 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00439-016-1667-5 |
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