Systematic analysis of paralogous regions in 41,755 exomes uncovers clinically relevant variation
As part of the study "Systematic analysis of paralogous regions in 41,755 exomes uncovers clinically relevant variation" we wanted to identiffy the SNVs that are located in STRC and which ones in STRCP1. For this we applied targeted long-read sequencing.
- 7 samples
- DAC: EGAC00001003397
- Technology: Ion Torrent Proton
STRC long-read sequencing for validation purposes in the Chameleolyser study
Sequencing data is available for researchers under controlled access
Studies are experimental investigations of a particular phenomenon, e.g., case-control studies on a particular trait or cancer research projects reporting matching cancer normal genomes from patients.
| Study ID | Study Title | Study Type |
|---|---|---|
| Other |