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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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Detalles Bibliográficos
Autores principales:	Nadukkalam Ravindran, Praveen, Bentzen, Paul, Bradbury, Ian R., Beiko, Robert G.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	John Wiley and Sons Inc. 2018
Materias:	Original Research
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6065343/ https://www.ncbi.nlm.nih.gov/pubmed/30073062 http://dx.doi.org/10.1002/ece3.4219

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