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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Bibliografiske detaljer
Udgivet i:Nucleic Acids Res
Main Authors: 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
Sprog:Inglês
Udgivet: Oxford University Press 2016
Fag:
Methods Online
Online adgang: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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