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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
Resource Name: PEMer
Resource ID: SCR_005263
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Source: SciCrunch Registry (RRID:SCR_005400)
Description: Interactive portal for finding and submitting biomedical resources. Resources within SciCrunch have assigned RRIDs which are used to cite resources in scientific manuscripts. SciCrunch Registry, formerly NIF Registry, provides resources catalog. Allows to add new resources. Allows edit existing resources after registration. Curators are tasked with identifying and registering resources, examining data, writing configuration files to index and display data and keeping contents current.
URL: https://rrid.site/rin/sources/SCR_005400
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