Targeted single molecule mutation detection with massively parallel sequencing

Next-generation sequencing (NGS) technologies have transformed genomic research and have the potential to revolutionize clinical medicine. However, the background error rates of sequencing instruments and limitations in targeted read coverage have precluded the detection of rare DNA sequence variant...

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Dades bibliogràfiques
Publicat a:Nucleic Acids Res
Autors principals: Gregory, Mark T., Bertout, Jessica A., Ericson, Nolan G., Taylor, Sean D., Mukherjee, Rithun, Robins, Harlan S., Drescher, Charles W., Bielas, Jason H.
Format: Artigo
Idioma:Inglês
Publicat: Oxford University Press 2016
Matèries:
Methods Online
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC4756847/
https://ncbi.nlm.nih.gov/pubmed/26384417
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/nar/gkv915
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