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Prioritisation of structural variant calls in cancer genomes

Sensitivity of short read DNA-sequencing for gene fusion detection is improving, but is hampered by the significant amount of noise composed of uninteresting or false positive hits in the data. In this paper we describe a tiered prioritisation approach to extract high impact gene fusion events from...

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Bibliografische gegevens
Gepubliceerd in:PeerJ
Hoofdauteurs: Ahdesmäki, Miika J., Chapman, Brad A., Cingolani, Pablo, Hofmann, Oliver, Sidoruk, Aleksandr, Lai, Zhongwu, Zakharov, Gennadii, Rodichenko, Mikhail, Alperovich, Mikhail, Jenkins, David, Carr, T. Hedley, Stetson, Daniel, Dougherty, Brian, Barrett, J. Carl, Johnson, Justin H.
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: PeerJ Inc. 2017
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Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC5382922/
https://ncbi.nlm.nih.gov/pubmed/28392986
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.7717/peerj.3166
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