The software and data listed here is partially under NSF and NIH support.
Available Software:
7. Fine mapping and test for sequence association.
Details can be found at:
Shaolong Cao, Huaizhen Qin, Hong-Wen Deng and Yu-Ping Wang, A unified sparse representation for sequence variant identification for complex traits.
Genetic epidemiology, 2014 Dec;38(8):671-9. doi: 10.1002/gepi.21849. Epub 2014 Sep 4.
Our data is also listed
Neuroimaging Informatics Tools and Resources Clearinghouse is currently a free one-stop-shop collaboratory for science researchers that need resources such as neuroimaging analysis software, publicly available data sets, or computing power.
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