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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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| Gepubliceerd in: | PeerJ |
|---|---|
| Hoofdauteurs: | , , , , , , , , , , , , , , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
PeerJ Inc.
2017
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| Onderwerpen: | |
| 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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