DeepSNVMiner: a sequence analysis tool to detect emergent, rare mutations in subsets of cell populations

Background. Massively parallel sequencing technology is being used to sequence highly diverse populations of DNA such as that derived from heterogeneous cell mixtures containing both wild-type and disease-related states. At the core of such molecule tagging techniques is the tagging and identificati...

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Detalles Bibliográficos
Autores principales: Andrews, T. Daniel, Jeelall, Yogesh, Talaulikar, Dipti, Goodnow, Christopher C., Field, Matthew A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PeerJ Inc. 2016
Materias:
Bioinformatics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4888318/
https://www.ncbi.nlm.nih.gov/pubmed/27257550
http://dx.doi.org/10.7717/peerj.2074

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4888318/
https://www.ncbi.nlm.nih.gov/pubmed/27257550
http://dx.doi.org/10.7717/peerj.2074

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