- Peter-Bram 't Hoen, Leiden University Medical Center
- Shane C Burgess, University of Arizona
- David Burt, University of Edinburgh
- John K Colbourne, The University of Birmingham
- Gustavo Goldman, FCFRP-Universidade de Sao Paulo
- Ivo G Gut, Centro Nacional de Analisis Genomico, Barcelona
- Scott E Hemby, Wake Forest University
- Hans Lehrach, Max Planck Institute for Molecular Genetics
- David Lightfoot, Southern Illinois University at Carbondale
- Paul Pavlidis, University of British Columbia
- Leonard Schalkwyk, King's College London
- Theo Smits, Zürich University for Applied Sciences
- Fabiano Thompson, UFRJ
- Stefan Wiemann, German Cancer Research Center
- Derek Anane, BioMed Central
Next Generation Sequencing provides a powerful tool in the elucidation of genomic content of organisms. QuickNGS utilises fully automated data analysis workflows to handle the large and complex datasets involved.
BMC Genomics 2015, 16:568
BMC Genomics is an open access, peer-reviewed journal that considers articles on all aspects of genome-scale analysis, functional genomics, and proteomics.
BMC Genomics is part of the BMC series which publishes subject-specific journals focused on the needs of individual research communities across all areas of biology and medicine. We offer an efficient, fair and friendly peer review service, and are committed to publishing all sound science, provided that there is some advance in knowledge presented by the work.
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Volume 16 Suppl 8 (18 June 2015)
VarI-SIG 2014: Identification and annotation of genetic variants in the context of structure, function and disease
Boston, MA, USA. 12 July 2014
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Selected articles from the International Conference on Intelligent Biology and Medicine (ICIBM) 2014: Genomics
San Antonio, TX, USA. 4-6 December 2014
Volume 16 Suppl 6 (1 June 2015)
Rome, Italy. 26-28 February 2014