Učitavanje...
GapFiller: a de novo assembly approach to fill the gap within paired reads
BACKGROUND: Next Generation Sequencing technologies are able to provide high genome coverages at a relatively low cost. However, due to limited reads' length (from 30 bp up to 200 bp), specific bioinformatics problems have become even more difficult to solve. De novo assembly with short reads,...
Spremljeno u:
| Glavni autori: | , , |
|---|---|
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
BioMed Central
2012
|
| Teme: | |
| Online pristup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3439727/ https://ncbi.nlm.nih.gov/pubmed/23095524 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2105-13-S14-S8 |
| Oznake: |
Dodaj oznaku
Bez oznaka, Budi prvi tko označuje ovaj zapis!
|