URL: http://sv.gersteinlab.org/pemer/
Proper Citation: PEMer (RRID:SCR_005263)
Description: Software package as computational framework with simulation-based error models for inferring genomic structural variants from massive paired-end sequencing data. Package is composed of three modules, PEMer workflow, SV-Simulation and BreakDB. PEMer workflow is a sensitive software for detecting SVs from paired-end sequence reads. SV-Simulation randomly introduces SVs into a given genome and generates simulated paired-end reads from novel genome.
Synonyms: Paired-End Mapper
Resource Type: software resource
Defining Citation: PMID:19236709
Keywords: structural variation, genome, next-generation sequencing, bio.tools, bio.tools
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