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URL: http://compbio.cs.sfu.ca/software-novelseq
Proper Citation: NovelSeq (RRID:SCR_003136)
Description: Software pipeline to detect novel sequence insertions using high throughput paired-end whole genome sequencing data.
Abbreviations: NovelSeq
Synonyms: NovelSeq: Novel Sequence Insertion Detection
Resource Type: software resource
Defining Citation: PMID:20385726
Keywords: sequence, insertion, genome sequencing, genome, next-generation sequencing, illumina, unix, linux, c, bio.tools
Availability: Free, Available for download, Freely available
Resource Name: NovelSeq
Resource ID: SCR_003136
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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
