## Abstract Copy number variations (CNVs) in the human genome provide exciting candidates for functional polymorphisms. Hence, we now assess association between CNV carrier status and diseases status by evaluating the signal intensity of SNP genotyping assays. Here, we present a novel statistical m
Bayesian data mining, with application to benchmarking and credit scoring
✍ Scribed by Paolo Giudici
- Publisher
- John Wiley and Sons
- Year
- 2001
- Tongue
- English
- Weight
- 128 KB
- Volume
- 17
- Category
- Article
- ISSN
- 1524-1904
- DOI
- 10.1002/asmb.425
No coin nor oath required. For personal study only.
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