Are you sure you want to leave this community? Leaving the community will revoke any permissions you have been granted in this community.
URL: http://bioinfo.au.tsinghua.edu.cn/software/DSGseq/
Proper Citation: DSGseq (RRID:SCR_001104)
Description: THIS RESOURCE IS NO LONGER IN SERVICE. Documented on August 15,2025. R software program for identifying differentially spliced genes from two groups of RNA-seq samples. It reads the count file and outputs the differences in the relative abundance of the isoforms of each gene in the annotation., THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025.
Abbreviations: DSGseq
Resource Type: software application, software resource, data analysis software, sequence analysis software, data processing software
Defining Citation: PMID:23228854
Keywords: rna seq, isoform, genes, spliced genes, r, genomics, sequence analysis software
Expand Allis listed by |
We found {{ ctrl2.mentions.all_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 DSGseq.
No alerts have been found for DSGseq.
Source: SciCrunch Registry