URL: https://github.com/mroosmalen/nanosv
Proper Citation: NanoSV (RRID:SCR_024127)
Description: Software package that can be used to identify structural genomic variations in long-read sequencing data, such as data produced by Oxford Nanopore Technologies� MinION, GridION or PromethION instruments, or Pacific Biosciences RSII or Sequel sequencers.
Synonyms: nanosv
Resource Type: software toolkit, software resource
Defining Citation: PMID:29109544
Keywords: identify structural genomic variations, long-read sequencing data, Oxford Nanopore Technologies� MinION, GridION, PromethION, Pacific Biosciences RSII, Sequel sequencers.
Expand Allis listed by |
We found {{ ctrl2.mentions.total_count }} mentions in open access literature.
We have not found any literature mentions for this resource.
We are searching literature mentions for this resource.
Most recent articles:
{{ mention._source.dc.creators[0].familyName }} {{ mention._source.dc.creators[0].initials }}, et al. ({{ mention._source.dc.publicationYear }}) {{ mention._source.dc.title }} {{ mention._source.dc.publishers[0].name }}, {{ mention._source.dc.publishers[0].volume }}({{ mention._source.dc.publishers[0].issue }}), {{ mention._source.dc.publishers[0].pagination }}. (PMID:{{ mention._id.replace('PMID:', '') }})
A list of researchers who have used the resource and an author search tool
A list of researchers who have used the resource and an author search tool. This is available for resources that have literature mentions.
No rating or validation information has been found for NanoSV.
No alerts have been found for NanoSV.
Source: SciCrunch Registry