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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...
Autores principales: | Andrews, T. Daniel, Jeelall, Yogesh, Talaulikar, Dipti, Goodnow, Christopher C., Field, Matthew A. |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
PeerJ Inc.
2016
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Materias: | |
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 |
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