URL: https://github.com/baneslab/iScanVCFMerge
Proper Citation: iScanVCFMerge (RRID:SCR_021193)
Description: Software Python package to merge cross species Illumina iScan genotype data with reference set of data from pre existing source.
Resource Type: data processing software, software application, software resource
Keywords: Illumina, iScan, Infinium, BeadArray, BeadChip, bead chip, SNP chip, genotyping, Illumina iScan genotype data, data reference set, merge cross species
Expand AllWe 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 iScanVCFMerge.
No alerts have been found for iScanVCFMerge.
Source: SciCrunch Registry