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Private Identified CNVs from whole exome sequencing data of BRCA1/2 negative breast c...
This dataset offers a comprehensive analysis of Copy Number Variations (CNVs) identified in Whole Exome Sequencing (WES) data from patients with breast cancer who tested... -
A hybrid approach for PPI
We propose a new framework that can exploit topological and biological information to predict protein-protein interactions. The algorithm relies on the underlying hypothesis... -
EpiCID: A framework for discovering interactions between SNPs
Epistatic interactions (EIs) of gene loci often determine complex trait phenotypes. EIs may indicate the underlying molecular mechanisms of multifactorial traits and diseases....