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CAGI4 Crohn’s exome challenge: Marker SNP versus exome variant models for assigning risk of Crohn disease
Understanding the basis of complex trait disease is a fundamental problem in human genetics. The CAGI Crohn’s Exome challenges are providing insight into the adequacy of current disease models by requiring participants to identify which of a set of individuals has been diagnosed with the disease, gi...
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| Udgivet i: | Hum Mutat |
|---|---|
| Main Authors: | , , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
2017
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5576730/ https://ncbi.nlm.nih.gov/pubmed/28512778 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/humu.23256 |
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