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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Hlavní autoři: Shigemizu, Daichi, Fujimoto, Akihiro, Akiyama, Shintaro, Abe, Tetsuo, Nakano, Kaoru, Boroevich, Keith A., Yamamoto, Yujiro, Furuta, Mayuko, Kubo, Michiaki, Nakagawa, Hidewaki, Tsunoda, Tatsuhiko
Médium: Artigo
Jazyk:Inglês
Vydáno: Nature Publishing Group 2013
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Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC3703611/
https://ncbi.nlm.nih.gov/pubmed/23831772
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/srep02161
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