scholarly journals Ten Simples Rules on How to Organise a Bioinformatics Hackathon

2021 ◽  
Vol 26 ◽  
pp. e983
Author(s):  
Susanne Hollmann ◽  
Babette Regierer ◽  
Teresa K Attwood ◽  
Andreas Gisel ◽  
Jacques Van Helden ◽  
...  

The completion of the human genome sequence triggered worldwide efforts to unravel the secrets hidden in its deceptively simple code. Numerous bioinformatics projects were undertaken to hunt for genes, predict their protein products, function and post-translational modifications, analyse protein-protein interactions, etc. Many novel analytic and predictive computer programmes fully optimised for manipulating human genome sequence data have been developed, whereas considerably less effort has been invested in exploring the many thousands of other available genomes, from unicellular organisms to plants and non-human animals.  Nevertheless, a detailed understanding of these organisms can have a significant impact on human health and well-being.New advances in genome sequencing technologies, bioinformatics, automation, artificial intelligence, etc., enable us to extend the reach of genomic research to all organisms.  To this aim gather, develop and implement new bioinformatics solutions (usually in the form of software) is pivotal. A helpful model, often used by the bioinformatics community, is the so-called hackathon. These are events when all stakeholders beyond their disciplines work together creatively to solve a problem. During its runtime, the consortium of the EU-funded project AllBio - Broadening the Bioinformatics Infrastructure to cellular, animal and plant science - conducted many successful hackathons with researchers from different Life Science areas. Based on this experience, in the following, the authors present a step-by-step and standardised workflow explaining how to organise a bioinformatics hackathon to develop software solutions to biological problems.

Blood ◽  
2010 ◽  
Vol 116 (21) ◽  
pp. SCI-16-SCI-16
Author(s):  
Eric D. Green

Abstract Abstract SCI-16 The Human Genome Project's completion of the human genome sequence in 2003 was a landmark scientific achievement of historic significance. It also signified a critical transition for the field of genomics, as the new foundation of genomic knowledge started to be used in powerful ways by researchers and clinicians to tackle increasingly complex problems in biomedicine. To exploit the opportunities provided by the human genome sequence and to ensure the productive growth of genomics as one of the most vital biomedical disciplines of the 21st century, the National Human Genome Research Institute (NHGRI) is pursuing a broad vision for genomics research beyond the Human Genome Project. This vision includes facilitating and supporting the highest-priority research areas that interconnect genomics to biology, to health, and to society.Current efforts in genomics research are focused on using genomic data, technologies, and insights to acquire a deeper understanding of biology and to uncover the genetic basis of human disease. Some of the most profound advances are being catalyzed by revolutionary new DNA sequencing technologies; these methods are already producing prodigious amounts of DNA sequence data, including from large numbers of individual patients. Such a capability, coupled with better associations between genetic diseases and specific regions of the human genome, are accelerating our understanding of the genetic basis for complex genetic disorders and for drug response. Together, these developments will usher in the era of genomic medicine. Disclosures: No relevant conflicts of interest to declare.


2001 ◽  
Vol 11 (20) ◽  
pp. R808-R811 ◽  
Author(s):  
Stephen W Scherer ◽  
Joseph Cheung

2010 ◽  
Vol 11 (11) ◽  
pp. 309 ◽  
Author(s):  
Amanda M Casto ◽  
Clara Amid

1998 ◽  
Vol 8 (11) ◽  
pp. 1097-1108 ◽  
Author(s):  
The Sanger Centre ◽  
The Washington University Genome Sequencing Cente

2011 ◽  
Vol 17 (2) ◽  
pp. 155-155
Author(s):  
Ewen Kirkness

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