ClipCrop: a tool for detecting structural variations with single-base resolution using soft-clipping information

BACKGROUND: Structural variations (SVs) change the structure of the genome and are therefore the causes of various diseases. Next-generation sequencing allows us to obtain a multitude of sequence data, some of which can be used to infer the position of SVs. METHODS: We developed a new method and imp...

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Detalles Bibliográficos
Autores principales: Suzuki, Shin, Yasuda, Tomohiro, Shiraishi, Yuichi, Miyano, Satoru, Nagasaki, Masao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Proceedings
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3287472/
https://www.ncbi.nlm.nih.gov/pubmed/22373054
http://dx.doi.org/10.1186/1471-2105-12-S14-S7

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3287472/
https://www.ncbi.nlm.nih.gov/pubmed/22373054
http://dx.doi.org/10.1186/1471-2105-12-S14-S7

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