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Novoalign used in the FAVR pipeline to determine rare genetic variants http://t.co/aR7qYXrPcq http://t.co/ClerFXCR9H
Novoalign used in the FAVR pipeline to determine rare genetic variants http://t.co/aR7qYXrPcq http://t.co/ClerFXCR9H
FAVR (Filtering and Annotation of Variants that are Rare): methods for analysis of rare variants http://t.co/ByPeO243Pe #bmcbioinformatics
RT @SAGRudd: FAVR: methods to facilitate analysis of rare germline genetic variants from #NGSeq = #magnificent @ http://t.co/yXKmnKRFb4
FAVR: methods to facilitate analysis of rare germline genetic variants from #NGSeq datasets = #magnificent @ http://t.co/vlsQaDSoNM