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PMERGE: Computational filtering of paralogous sequences from RAD‐seq data
Restriction‐site associated DNA sequencing (RAD‐seq) can identify and score thousands of genetic markers from a group of samples for population‐genetics studies. One challenge of de novo RAD‐seq analysis is to distinguish paralogous sequence variants (PSVs) from true single‐nucleotide polymorphisms...
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Publicado no: | Ecol Evol |
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Main Authors: | , , , |
Formato: | Artigo |
Idioma: | Inglês |
Publicado em: |
John Wiley and Sons Inc.
2018
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Assuntos: | |
Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6065343/ https://ncbi.nlm.nih.gov/pubmed/30073062 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ece3.4219 |
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