URL: https://github.com/Illumina/manta
Proper Citation: Manta (RRID:SCR_022997)
Description: Software tool for rapid detection of structural variants and indels for germline and cancer sequencing applications. Used to call structural variants and indels from mapped paired end sequencing reads.
Resource Type: data analysis software, data processing software, sequence analysis software, software application, software resource
Defining Citation: PMID:26647377
Keywords: rapid detection, structural variants and indels, mapped paired end sequencing reads, structural variant, indel
Availability: Free, Available for download, Freely available
Resource Name: Manta
Resource ID: SCR_022997
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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
