URL: http://compbio.bccrc.ca/software/jointsnvmix/
Proper Citation: JointSNVMix (RRID:SCR_006804)
Description: Software that implements a probabilistic graphical model to analyze sequence data from tumor / normal pairs. The model draws statistical strength by analysing both genome jointly to more accurately classify germline and somatic mutations. It effectively reduces false positive somatic mutation predictions in tumour-normal pair sequencing data. It is highly recommended to post-process results with mutationSeq in order to filter technical artifacts.
Abbreviations: JointSNVMix
Resource Type: data analysis software, software application, data processing software, software resource
Defining Citation: PMID:22285562
Keywords: tumor, cancer, normal, somatic mutation, mutation
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