Furthering data analysis of next-generation sequencing to facilitate research

Reporting their platform in Genome Biology, scientists say that the new platform--called BioWardrobe--could help biomedical researchers answer questions about both basic biology and disease.

The recent proliferation of next-generation sequencing (NGS)-based methods for analysis of gene expression, chromatin structure and protein-DNA interactions have opened new horizons for molecular biology. These methods include RNA sequencing (RNA-Seq), chromatin immunoprecipitation sequencing (ChIP-Seq), DNase I sequencing (DNase-Seq), micrococcal nuclease sequencing (MNase-Seq), assay for transposase-accessible chromatin sequencing (ATAC-Seq) and others.

The sheer volume of the data obtained from sequencing requires computational data analysis. However, the bioinformatics and programming expertise required for this analysis is usually absent in typical biomedical laboratories, according to the authors. This results in data inaccessibility or delays in applying modern sequencing-based technologies to pressing questions in basic and health-related research.

"Although biologists can perform experiments and obtain the data, they often lack the programming expertise required to perform computational data analysis," says Artem Barski, PhD, senior author and assistant professor in the Divisions of Allergy and Immunology and Human Genetics at Cincinnati Children's. "BioWardrobe aims to empower researchers by bridging this gap between data and knowledge."

Andrey Kartashov, MS and Barski collaboratively developed BioWardrobe to facilitate the analysis and utilization of both newly generated and publically available datasets.

"Huge amounts of published data have been deposited in public databases, such as Gene Expression Omnibus or Short Read Archive, but remain inaccessible to majority of researchers due to lack of bioinformatics expertise," Kartashov said. "BioWardrobe allows biologists to analyze the data without having to learn how to program."