Optimized detection of insertions/deletions (INDELs) in whole-exome sequencing data

Insertion and deletion (INDEL) mutations, the most common type of structural variance, are associated with several human diseases. The detection of INDELs through next-generation sequencing (NGS) is becoming more common due to the decrease in costs, the increase in efficiency, and sensitivity improv...

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Detalles Bibliográficos
Autores principales: Kim, Bo-Young, Park, Jung Hoon, Jo, Hye-Yeong, Koo, Soo Kyung, Park, Mi-Hyun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5549930/
https://www.ncbi.nlm.nih.gov/pubmed/28792971
http://dx.doi.org/10.1371/journal.pone.0182272

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5549930/
https://www.ncbi.nlm.nih.gov/pubmed/28792971
http://dx.doi.org/10.1371/journal.pone.0182272

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