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URL: https://software.broadinstitute.org/software/discovar/blog/
Proper Citation: Discovar assembler (RRID:SCR_016755)
Description: Software tool for variant calling with reference and de novo assembly of genomes. The heart of DISCOVAR is a de novo genome assembler which can generate de novo assemblies for both large and small genomes.
Abbreviations: Discovar
Synonyms: Discovar de novo, Discovar
Resource Type: data analysis software, data processing software, sequence analysis software, software application, software resource
Defining Citation: PMID:25326702
Keywords: variant, calling, reference, de novo, assembly, genome, genetic, human, sequence, analysis
Funding: NHGRI R01 HG003474; NHGRI U54 HG003067; NIAID HHSN272200900018C
Availability: Free, Available for download, Freely available
Resource Name: Discovar assembler
Resource ID: SCR_016755
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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