Here we describe a prediction-based framework to analyze omic data and generate models for both disease diagnosis and identification of cellular pathways which are significant in complex diseases. Our framework differs from previous analysis in its use of underlying biology (cellular pathways/gene-sets) to produce predictive feature-disease models. In our study of alcoholism, lung cancer, and schizophrenia, we demonstrate the framework’s ability to robustly analyze omic data of multiple types and sources, identify significant features sets, and produce accurate predictive models
Various tools have been recently developed to integrate such datasets, but there are limited strateg...
Motivation: Gene set enrichment analysis (GSEA) annotates gene microarray data with functional infor...
Most human common diseases are complex traits that are controlled by genetic variants in multiple ge...
textThe completion of the human genome project has led to a flood of new genetic data, that has prov...
High-throughput data have become ubiquitous in the study of biological phenomena. We can now query c...
The development of high-throughput biotechnologies have made data accessible from different platform...
The main challenge for gaining biological insights from genetic associations is identifying which ge...
The main challenge for gaining biological insights from genetic associations is identifying which ge...
Genomic prediction has the potential to contribute to precision medicine. However, to date, the util...
High-confidence prediction of complex traits such as disease risk or drug response is an ultimate go...
Summary: We present MutaGeneSys: a system that uses genomewide genotype data for disease prediction....
Background: Large collections of paraffin-embedded tissue represent a rich resource to test hypothes...
Cancer research, like many areas of science, is adapting to a new era characterized by increasing qu...
BACKGROUND: The identification of genes involved in human complex diseases remains a great challenge...
Background: Over the past decades, approaches for diagnosing and treating cancer have seen significa...
Various tools have been recently developed to integrate such datasets, but there are limited strateg...
Motivation: Gene set enrichment analysis (GSEA) annotates gene microarray data with functional infor...
Most human common diseases are complex traits that are controlled by genetic variants in multiple ge...
textThe completion of the human genome project has led to a flood of new genetic data, that has prov...
High-throughput data have become ubiquitous in the study of biological phenomena. We can now query c...
The development of high-throughput biotechnologies have made data accessible from different platform...
The main challenge for gaining biological insights from genetic associations is identifying which ge...
The main challenge for gaining biological insights from genetic associations is identifying which ge...
Genomic prediction has the potential to contribute to precision medicine. However, to date, the util...
High-confidence prediction of complex traits such as disease risk or drug response is an ultimate go...
Summary: We present MutaGeneSys: a system that uses genomewide genotype data for disease prediction....
Background: Large collections of paraffin-embedded tissue represent a rich resource to test hypothes...
Cancer research, like many areas of science, is adapting to a new era characterized by increasing qu...
BACKGROUND: The identification of genes involved in human complex diseases remains a great challenge...
Background: Over the past decades, approaches for diagnosing and treating cancer have seen significa...
Various tools have been recently developed to integrate such datasets, but there are limited strateg...
Motivation: Gene set enrichment analysis (GSEA) annotates gene microarray data with functional infor...
Most human common diseases are complex traits that are controlled by genetic variants in multiple ge...