Making the most of RNA-seq: Pre-processing sequencing data with Opossum for reliable SNP variant detection [version 2; referees: 2 approved, 1 approved with reservations]
Identifying variants from RNA-seq (transcriptome sequencing) data is a cost-effective and versatile complement to whole-exome (WES) and whole-genome sequencing (WGS) analysis. RNA-seq (transcriptome sequencing) is primarily considered a method of gene expression analysis but it can also be used to d...
| Main Authors: | , |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
Wellcome
2017-03-01
|
| Series: | Wellcome Open Research |
| Subjects: | |
| Online Access: | https://wellcomeopenresearch.org/articles/2-6/v2 |