VCF2CAPS–A high-throughput CAPS marker design from VCF files and its test-use on a genotyping-by-sequencing (GBS) dataset

Next-generation sequencing (NGS) is a powerful tool for massive detection of DNA sequence variants such as single nucleotide polymorphisms (SNPs), multi-nucleotide polymorphisms (MNPs) and insertions/deletions (indels). For routine screening of numerous samples, these variants are often converted in...

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Detalles Bibliográficos
Autores principales: Wesołowski, Wojciech, Domnicz, Beata, Augustynowicz, Joanna, Szklarczyk, Marek
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2021
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8186816/
https://www.ncbi.nlm.nih.gov/pubmed/34014924
http://dx.doi.org/10.1371/journal.pcbi.1008980

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8186816/
https://www.ncbi.nlm.nih.gov/pubmed/34014924
http://dx.doi.org/10.1371/journal.pcbi.1008980

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