Wordt geladen...
PSE-HMM: genome-wide CNV detection from NGS data using an HMM with Position-Specific Emission probabilities
BACKGROUND: Copy Number Variation (CNV) is envisaged to be a major source of large structural variations in the human genome. In recent years, many studies apply Next Generation Sequencing (NGS) data for the CNV detection. However, still there is a necessity to invent more accurate computational too...
Bewaard in:
| Gepubliceerd in: | BMC Bioinformatics |
|---|---|
| Hoofdauteurs: | , , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
BioMed Central
2016
|
| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5445519/ https://ncbi.nlm.nih.gov/pubmed/27809781 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12859-016-1296-y |
| Tags: |
Voeg label toe
Geen labels, Wees de eerste die dit record labelt!
|