Laddar...
Rare variants analysis using penalization methods for whole genome sequence data
BACKGROUND: Availability of affordable and accessible whole genome sequencing for biomedical applications poses a number of statistical challenges and opportunities, particularly related to the analysis of rare variants and sparseness of the data. Although efforts have been devoted to address these...
Sparad:
| I publikationen: | BMC Bioinformatics |
|---|---|
| Huvudupphovsmän: | , , |
| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
BioMed Central
2015
|
| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4670502/ https://ncbi.nlm.nih.gov/pubmed/26637205 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12859-015-0825-4 |
| Taggar: |
Lägg till en tagg
Inga taggar, Lägg till första taggen!
|