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...

Descripción completa

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

Internet

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

Ejemplares similares