Laddar...
Mapping short DNA sequencing reads and calling variants using mapping quality scores
New sequencing technologies promise a new era in the use of DNA sequence. However, some of these technologies produce very short reads, typically of a few tens of base pairs, and to use these reads effectively requires new algorithms and software. In particular, there is a major issue in efficiently...
Sparad:
| Huvudupphovsmän: | , , |
|---|---|
| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
Cold Spring Harbor Laboratory Press
2008
|
| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2577856/ https://ncbi.nlm.nih.gov/pubmed/18714091 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1101/gr.078212.108 |
| Taggar: |
Lägg till en tagg
Inga taggar, Lägg till första taggen!
|