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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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| Publicat a: | PLoS One |
|---|---|
| Autors principals: | , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Public Library of Science
2020
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| Matèries: | |
| Accés en línia: | 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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