Indel sensitive and comprehensive variant/mutation detection from RNA sequencing data for precision medicine

BACKGROUND: RNA-seq is the most commonly used sequencing application. Not only does it measure gene expression but it is also an excellent media to detect important structural variants such as single nucleotide variants (SNVs), insertion/deletion (Indels) or fusion transcripts. However, detection of...

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Detalles Bibliográficos
Autores principales: Prodduturi, Naresh, Bhagwate, Aditya, Kocher, Jean-Pierre A., Sun, Zhifu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6157028/
https://www.ncbi.nlm.nih.gov/pubmed/30255803
http://dx.doi.org/10.1186/s12920-018-0391-5

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6157028/
https://www.ncbi.nlm.nih.gov/pubmed/30255803
http://dx.doi.org/10.1186/s12920-018-0391-5

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