A practical method to detect SNVs and indels from whole genome and exome sequencing data

The recent development of massively parallel sequencing technology has allowed the creation of comprehensive catalogs of genetic variation. However, due to the relatively high sequencing error rate for short read sequence data, sophisticated analysis methods are required to obtain high-quality varia...

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Detalles Bibliográficos
Autores principales: Shigemizu, Daichi, Fujimoto, Akihiro, Akiyama, Shintaro, Abe, Tetsuo, Nakano, Kaoru, Boroevich, Keith A., Yamamoto, Yujiro, Furuta, Mayuko, Kubo, Michiaki, Nakagawa, Hidewaki, Tsunoda, Tatsuhiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2013
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3703611/
https://www.ncbi.nlm.nih.gov/pubmed/23831772
http://dx.doi.org/10.1038/srep02161

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3703611/
https://www.ncbi.nlm.nih.gov/pubmed/23831772
http://dx.doi.org/10.1038/srep02161

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