The software and data listed here is partially under NSF and NIH support.
Available Software:
5. Copy number variation (CNV) detection from exome sequencing data using a sparse model
Details can be found at:
J. Duan, M. Wan, H.-W. Deng, and Y.-P. Wang, "A sparse model based detection of copy number variations from exome sequencing data," IEEE Trans.
Biomedical Engineering, in review, 2015.
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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