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Minimum error correction-based haplotype assembly: Considerations for long read data
The single nucleotide polymorphism (SNP) is the most widely studied type of genetic variation. A haplotype is defined as the sequence of alleles at SNP sites on each haploid chromosome. Haplotype information is essential in unravelling the genome-phenotype association. Haplotype assembly is a well-k...
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| Yayımlandı: | PLoS One |
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| Asıl Yazarlar: | , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Public Library of Science
2020
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7292361/ https://ncbi.nlm.nih.gov/pubmed/32530974 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0234470 |
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