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» Closest Pairs Data Selection for Support Vector Machines
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BMCBI
2008
99views more  BMCBI 2008»
13 years 7 months ago
Exhaustive prediction of disease susceptibility to coding base changes in the human genome
Background: Single Nucleotide Polymorphisms (SNPs) are the most abundant form of genomic variation and can cause phenotypic differences between individuals, including diseases. Ba...
Vinayak Kulkarni, Mounir Errami, Robert Barber, Ha...
MICCAI
2010
Springer
13 years 5 months ago
Biomarkers for Identifying First-Episode Schizophrenia Patients Using Diffusion Weighted Imaging
Recent advances in diffusion weighted MR imaging (dMRI) has made it a tool of choice for investigating white matter abnormalities of the brain and central nervous system. In this w...
Yogesh Rathi, James G. Malcolm, Oleg V. Michailovi...