Lataa...
SEQCHIP: a powerful method to integrate sequence and genotype data for the detection of rare variant associations
Motivation: Next-generation sequencing greatly increases the capacity to detect rare-variant complex-trait associations. However, it is still expensive to sequence a large number of samples and therefore often small datasets are used. Given cost constraints, a potentially more powerful two-step stra...
Tallennettuna:
| Päätekijät: | , |
|---|---|
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Oxford University Press
2012
|
| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3381973/ https://ncbi.nlm.nih.gov/pubmed/22556370 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/bts263 |
| Tagit: |
Lisää tagi
Ei tageja, Lisää ensimmäinen tagi!
|