Open Access

Editorial

  • Vasilis Vasiliou1
Human Genomics20115:137

https://doi.org/10.1186/1479-7364-5-3-137

Published: 1 March 2011

I would like to welcome you to Volume 5, Issue 3 of Human Genomics. As discussed in Issue 2, we have introduced the open-access opportunity for papers published in the Journal. Our instructions to authors have been revised to reflect this change and to include other modifications that will improve the submission process. The instructions to authors can be found at the end of this issue on p. 208.

Our submission rate has increased and our publication rate is constant to the point that our Impact Factor will be provided by ISI by the summer of 2011.

We have a new addition to our Editorial Board. I therefore welcome and introduce to you, Samir Zakhari, who is Director of the Division of Metabolism and Health Effects of the National Institute on Alcohol Abuse and Alcoholism at the National Institutes of Health, USA.

In this issue, we start with the Research Highlights. Webb, Smith and Cotton then describe the difficulties associated with finding SNPs and related phenotypic data in world wide web resources using simple, uncomplicated search terms and they also provide a suggested solution. This is followed by the Filocamo and Morrone Review of the molecular basis and laboratory testing of lysosomal storage disorders, a group of more than 50 different inherited metabolic diseases. In the Update on Gene Completions and Annotations section, Smathers and Petersen review the human fatty acid-binding protein (FABP) family, a member to the superfamily of intracellular lipid-binding proteins. In this paper, the evolutionary divergences and functions of the FABPs are discussed. In Issue 5.2, Wright and Bruford provided an excellent Review on the nomenclature of non-coding RNAs (pp. 90-98). In the Software Review section of the current issue, Agirre and Eyras discuss databases and resources available for non-coding RNAs (sRNAs). They look at the main issues related to the integration and annotation of sRNA datasets. In the Genome Databases section, Valerio discusses toxicology models and databases as Critical Path toolkits for predicting toxicities early in drug development. Finally, Cassiman reviews the second edition of a book entitled 'Molecular Diagnostics' published by Elsevier (Academic Press) in 2010 and edited by George Patrinos and Wilhelm Ansorge.

Authors’ Affiliations

(1)
Editor, Human Genomics University of Colorado

Copyright

© Henry Stewart Publications 2011

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