Analysing 454 amplicon resequencing experiments using the modular and database oriented Variant Identification Pipeline

BACKGROUND: Next-generation amplicon sequencing enables high-throughput genetic diagnostics, sequencing multiple genes in several patients together in one sequencing run. Currently, no open-source out-of-the-box software solution exists that reliably reports detected genetic variations and that can...

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Hlavní autoři: De Schrijver, Joachim M, De Leeneer, Kim, Lefever, Steve, Sabbe, Nick, Pattyn, Filip, Van Nieuwerburgh, Filip, Coucke, Paul, Deforce, Dieter, Vandesompele, Jo, Bekaert, Sofie, Hellemans, Jan, Van Criekinge, Wim
Médium: Artigo
Jazyk:Inglês
Vydáno: BioMed Central 2010
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On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC2880033/
https://ncbi.nlm.nih.gov/pubmed/20487544
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2105-11-269
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