Loading...
TIDDIT, an efficient and comprehensive structural variant caller for massive parallel sequencing data
Reliable detection of large structural variation ( > 1000 bp) is important in both rare and common genetic disorders. Whole genome sequencing (WGS) is a technology that may be used to identify a large proportion of the genomic structural variants (SVs) in an individual in a single experiment. Eve...
Na minha lista:
| Udgivet i: | F1000Res |
|---|---|
| Main Authors: | , , , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
F1000Research
2017
|
| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5521161/ https://ncbi.nlm.nih.gov/pubmed/28781756 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.12688/f1000research.11168.2 |
| Tags: |
Tilføj Tag
Ingen Tags, Vær først til at tagge denne postø!
|