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URL: http://sourceforge.net/projects/ngsep/
Proper Citation: NGSEP (RRID:SCR_012827)
Description: Software whose main functionality is the variants detector, which allows to make simultaneous discovery of SNVs, small indels, and CNVs.Accurate variant calling across species and sequencing protocols.Used for analysis of DNA high throughput sequencing data.
Abbreviations: NGSEP
Synonyms: NGSEP3, Next Generation Sequencing Eclipse Plugin, Next Generation Sequencing Experience Platform
Resource Type: data analysis software, data processing software, software application, software resource
Defining Citation: PMID:31099384
Keywords: matlab, variants detector, SNVs discovery, CNVs discovery, variant calling, species, sequencing protocols, bio.tools
Availability: Free, Available for download, Freely available
Resource Name: NGSEP
Resource ID: SCR_012827
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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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