SNVMix: predicting single nucleotide variants from next-generation sequencing of tumors

Motivation: Next-generation sequencing (NGS) has enabled whole genome and transcriptome single nucleotide variant (SNV) discovery in cancer. NGS produces millions of short sequence reads that, once aligned to a reference genome sequence, can be interpreted for the presence of SNVs. Although tools ex...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Päätekijät: Goya, Rodrigo, Sun, Mark G.F., Morin, Ryan D., Leung, Gillian, Ha, Gavin, Wiegand, Kimberley C., Senz, Janine, Crisan, Anamaria, Marra, Marco A., Hirst, Martin, Huntsman, David, Murphy, Kevin P., Aparicio, Sam, Shah, Sohrab P.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Oxford University Press 2010
Aiheet:
Original Papers
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC2832826/
https://ncbi.nlm.nih.gov/pubmed/20130035
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/btq040
Tagit: Lisää tagi
Ei tageja, Lisää ensimmäinen tagi!

Samankaltaisia teoksia