Massively parallel sequencing of the mouse exome to accurately identify rare, induced mutations: an immediate source for thousands of new mouse models

Accurate identification of sparse heterozygous single-nucleotide variants (SNVs) is a critical challenge for identifying the causative mutations in mouse genetic screens, human genetic diseases and cancer. When seeking to identify causal DNA variants that occur at such low rates, they are overwhelme...

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Detalles Bibliográficos
Autores principales: Andrews, T. D., Whittle, B., Field, M. A., Balakishnan, B., Zhang, Y., Shao, Y., Cho, V., Kirk, M., Singh, M., Xia, Y., Hager, J., Winslade, S., Sjollema, G., Beutler, B., Enders, A., Goodnow, C. C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2012
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3376740/
https://www.ncbi.nlm.nih.gov/pubmed/22724066
http://dx.doi.org/10.1098/rsob.120061

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3376740/
https://www.ncbi.nlm.nih.gov/pubmed/22724066
http://dx.doi.org/10.1098/rsob.120061

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