Učitavanje...
SVM(2): an improved paired-end-based tool for the detection of small genomic structural variations using high-throughput single-genome resequencing data
Several bioinformatics methods have been proposed for the detection and characterization of genomic structural variation (SV) from ultra high-throughput genome resequencing data. Recent surveys show that comprehensive detection of SV events of different types between an individual resequenced genome...
Spremljeno u:
| Glavni autori: | , , |
|---|---|
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
Oxford University Press
2012
|
| Teme: | |
| Online pristup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3467043/ https://ncbi.nlm.nih.gov/pubmed/22735696 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/nar/gks606 |
| Oznake: |
Dodaj oznaku
Bez oznaka, Budi prvi tko označuje ovaj zapis!
|