Next Generation Sequencing Newsletter June 2013

Next Generation Sequencing Newsletter

June 2013

NextGenSeq@nature.com provides a feel for the current state of the art in next generation sequencing technologies and how these platforms are changing the face of biomedical research. The page hosts a collection of original research, commentary and reviews published by Nature Publishing Group. Sign up for monthly e-alerts from Next Generation Sequencing.

Highlighted articles Access these articles for FREE by visiting NextGenSeq@nature.com   Comparative analysis of RNA sequencing methods for degraded or low-input samples FREE Xian Adiconis, Diego Borges-Rivera, Rahul Satija, David S DeLuca, Michele A Busby, Aaron M Berlin, Andrey Sivachenko, Dawn Anne Thompson, Alec Wysoker, Timothy Fennell, Andreas Gnirke, Nathalie Pochet, Aviv Regev & Joshua Z Levin Nature Methods doi:10.1038/nmeth.2483   The use of next-generation sequencing in clinical diagnosis of familial hypercholesterolemia FREE Jana Vandrovcova, Ellen R.A. Thomas, Santosh S Atanur, Penny J. Norsworthy, Clare Neuwirth, Yvonne Tan, Dalia Kasperaviciute, Jennifer Biggs, Laurence Game, Michael Mueller, Anne K. Soutar & Timothy J. Aitman Genetics in Medicine doi:10.1038/gim.2013.55   Exome sequencing as a diagnostic tool to identify a causal mutation in genetically highly heterogeneous limb-girdle muscular dystrophy FREE Tohru Matsuura, Tatsuaki Kurosaki, Yoshio Omote, Narihiro Minami, Yukiko K Hayashi, Ichizo Nishino & Koji Abe Journal of Human Genetics doi:10.1038/jhg.2013.33   Commercial prospects for genomic sequencing technologies FREE Sharmarke Mohamed & Basharut A. Syed Nature Reviews Drug Discovery doi:10.1038/nrd4006 NPG journal-based collections of interest   Applications of next–generation sequencing (Series in Nature Reviews Genetics)   Focus on Next-Generation Sequencing (Supplement from Nature Biotechnology) Recent articles from NPG Access these articles by visiting NextGenSeq@nature.com   Panel-based next generation sequencing as a reliable and efficient technique to detect mutations in unselected patients with retinal dystrophies Nicola Glöckle, Susanne Kohl, Julia Mohr, Tim Scheurenbrand, Andrea Sprecher, Nicole Weisschuh, Antje Bernd, Günther Rudolph, Max Schubach, Charlotte Poloschek, Eberhart Zrenner, Saskia Biskup, Wolfgang Berger, Bernd Wissinger & John Neidhardt European Journal of Human Genetics doi:10.1038/ejhg.2013.72   Cancer genome-sequencing study design Jill C. Mwenifumbo & Marco A. Marra Nature Reviews Genetics doi:10.1038/nrg3445   Molecular genetic testing and the future of clinical genomics Sara Huston Katsanis & Nicholas Katsanis Nature Reviews Genetics doi:10.1038/nrg3493   Whole-genome sequencing in health care Carla G van El, Martina C Cornel, Pascal Borry, Ros J Hastings, Florence Fellmann, Shirley V Hodgson, Heidi C Howard, Anne Cambon-Thomsen, Bartha M Knoppers, Hanne Meijers-Heijboer, Hans Scheffer, Lisbeth Tranebjaerg, Wybo Dondorp & Guido M W R de Wert European Journal of Human Genetics doi:10.1038/ejhg.2013.46   Epigenomic strategies at the interface of genetic and environmental risk factors for autism Janine M LaSalle Journal of Human Genetics doi:10.1038/jhg.2013.49   Genome-Wide Epigenetics Brian C Capell & Shelley L Berger Journal of Investigative Dermatology doi:10.1038/jid.2013.173

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