Tranchevent LC

ORCID: 0000-0002-1257-4824 · 6 papers in corpus
2010
Genome medicine ·doi:10.1186/gm137

BackgroundHow to efficiently integrate the daily practice of molecular biologists, geneticists, and clinicians with the emerging computational strategies from systems biology is still much of an open question.DescriptionWe built on the rece…

2010
BMC bioinformatics ·doi:10.1186/1471-2105-11-28

BackgroundText mining has become a useful tool for biologists trying to understand the genetics of diseases. In particular, it can help identify the most interesting candidate genes for a disease for further experimental analysis. Many text…

2010
BMC bioinformatics ·doi:10.1186/1471-2105-11-309

BackgroundThis paper introduces the notion of optimizing different norms in the dual problem of support vector machines with multiple kernels. The selection of norms yields different extensions of multiple kernel learning (MKL) such as L(in…

2009
PLoS genetics ·doi:10.1371/journal.pgen.1000351

Genetic screens are powerful methods for the discovery of gene-phenotype associations. However, a systems biology approach to genetics must leverage the massive amount of "omics" data to enhance the power and speed of functional gene discov…

2009
PloS one ·doi:10.1371/journal.pone.0005526

Genetic studies (in particular linkage and association studies) identify chromosomal regions involved in a disease or phenotype of interest, but those regions often contain many candidate genes, only a few of which can be followed-up for bi…

2008
Nucleic acids research ·doi:10.1093/nar/gkn325

Endeavour (http://www.esat.kuleuven.be/endeavourweb; this web site is free and open to all users and there is no login requirement) is a web resource for the prioritization of candidate genes. Using a training set of genes known to be invol…