Australian open source drag-and-drop GUI boosts genomic DNA research

| No Comments
| More

Western Australia's Murdoch University has pioneered an open source project designed to build drag-and-drop style web-based user interfaces suitable for supercomputers.

While the particle physicist, computer science and computational physics communities are all comparatively adept when it comes to juggling command line level code operation, the same skills do not typically translate over to the men in white coats tasked with looking after comparative genomics research.

NOTE: news-medical.net defines Genomics as: the study of the genomes of organisms -- the field includes efforts to determine the entire deoxyribonucleic acid (DNA) sequence of organisms and fine-scale genetic mapping efforts. The human biological data contained in a genome is encoded in its DNA structures, which is then subdivided into 'discrete units' called genes.

Scientists at Murdoch University set out to build Yabi to simplify access to supercomputing infrastructures for end users.

Genomics_GTL_Pictorial_Program.jpg

Free image: Wikimedia Commons

"Yabi has radically transformed the way we process and analyse 2nd generation DNA sequence data. Through a user-friendly dynamic HTML interface we can design a simple pipeline that sorts, trims and queries sequence data against databases -- we put raw data in one end and obtain meaningful outputs at the end of the pipeline. Put simply, Yabi has enabled us to spend more time analysing the actual data and less time 'fighting' it," said Dr Michael Bunce, ARC Future Fellow, Ancient DNA Lab, School of Biological Sciences and Biotechnology, Murdoch University.

In related news...

Graphical Processing Unit (GPU) specialist Nvidia has detailed updates concerning news that the world's largest genomics institute is launching a cloud-based next-generation sequencing (NGS) bioinformatics research service accelerated by Nvidia hardware.

China-based BGI has combined automated pipeline analysis with software and tools to be integrated with the industry's largest sequencing platform. The intention is to provide information for biologists, bioinformaticists and physicians to submit and receive an automated analysis of DNA sequencing data.

The question remains -- how many bioinformaticists, particle physicists and computational physics specialists does it take to change a light bulb?

Leave a comment

(You will need either to sign in or enter a valid email address to comment.)

About this Entry

This page contains a single entry by Adrian Bridgwater published on April 30, 2012 9:47 AM.

IBM plays nice with Red Hat and SUSE on Linux, Canonical not in the gang was the previous entry in this blog.

Kanban (カンバン) Toyota Just-In-Time techniques for social coding is the next entry in this blog.

Find recent content on the main index or look in the archives to find all content.

Categories

Archives

-- Advertisement --