URL: http://genetics.cs.ucla.edu/harsh/
Proper Citation: HARSH (RRID:SCR_010792)
Description: Software that provides a method to infer the haplotype using haplotype reference panel and high throughput sequencing data.
Abbreviations: HARSH
Synonyms: HAplotype inference using Reference and Sequencing tecHnology
Resource Type: software resource
Keywords: bio.tools
Expand Allis listed by |
|
is listed by |
|
is listed by |
|
has parent organization |
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:', '') }})
Check
for all resource mentions.
A list of researchers who have used the resource and an author search tool
Find mentions based on location
{{ ctrl2.mentions.errors.location }}
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 HARSH.
No alerts have been found for HARSH.
Source: SciCrunch Registry
