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Phasing of single DNA molecules by massively parallel barcoding

High-throughput sequencing platforms mainly produce short-read data, resulting in a loss of phasing information for many of the genetic variants analysed. For certain applications, it is vital to know which variant alleles are connected to each individual DNA molecule. Here we demonstrate a method f...

詳細記述

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書誌詳細
出版年:Nat Commun
主要な著者: Borgström, Erik, Redin, David, Lundin, Sverker, Berglund, Emelie, Andersson, Anders F., Ahmadian, Afshin
フォーマット: Artigo
言語:Inglês
出版事項: Nature Pub. Group 2015
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC4468844/
https://ncbi.nlm.nih.gov/pubmed/26055759
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ncomms8173
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