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Resource Name
mutationSeq
RRID:SCR_006815 RRID Copied      
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mutationSeq (RRID:SCR_006815)
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Resource Information

URL: http://compbio.bccrc.ca/software/mutationseq/

Proper Citation: mutationSeq (RRID:SCR_006815)

Description: A software suite using feature-based classifiers for somatic mutation prediction from paired tumour/normal next-generation sequencing data. mutationSeq has the advantages of integrating different features (e.g., base qualities, mapping qualities, strand bias, and tailed distance features), and validated somatic mutations to make predictions. Given paired normal/tumour bam files, mutationSeq will output the probability of each candidate site being somatic.

Abbreviations: mutationSeq

Resource Type: software resource

Defining Citation: PMID:22084253

Keywords: next-generation sequencing, somatic mutation, tumor, normal

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This resource

is listed by

OMICtools

is related to

JointSNVMix

has parent organization

BC Cancer Agency

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