Tandem-genotypes: robust detection of tandem repeat expansions from long DNA reads

Tandemly repeated DNA is highly mutable and causes at least 31 diseases, but it is hard to detect pathogenic repeat expansions genome-wide. Here, we report robust detection of human repeat expansions from careful alignments of long but error-prone (PacBio and nanopore) reads to a reference genome. O...

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Detalles Bibliográficos
Autores principales: Mitsuhashi, Satomi, Frith, Martin C., Mizuguchi, Takeshi, Miyatake, Satoko, Toyota, Tomoko, Adachi, Hiroaki, Oma, Yoko, Kino, Yoshihiro, Mitsuhashi, Hiroaki, Matsumoto, Naomichi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Method
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6425644/
https://www.ncbi.nlm.nih.gov/pubmed/30890163
http://dx.doi.org/10.1186/s13059-019-1667-6

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6425644/
https://www.ncbi.nlm.nih.gov/pubmed/30890163
http://dx.doi.org/10.1186/s13059-019-1667-6

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