Last Posted: Jan-18-2017 4PM
From CDC Information Database
This database includes general CDC public health information on specific diseases and health related topics. When available, the database displays genomic information from various CDC web pages. Users are also encouraged to conduct searches of CDC website for additional information.
- Using whole genome sequencing to transform tuberculosis outbreak detection and surveillance
- AMD Projects: Analyzing Emerging Epidemics
Whole genome sequencing to assess epidemic potential of emerging meningococcal strains and monitor changes in vaccine immunogen and virulence-related genes - Using whole genome sequencing and metagenomics to identify and track tickborne pathogens
- Genome Sequencing in the Clinic – The question is not whether the glass is half-full or half-empty but whether or not the glass is the right tool.
Genomics and Health Impact Blog - When Should We All Have Our Genomes Sequenced?
Genomics and Health Impact Blog - When Should We All Have Our Genomes Sequenced?
Genomics and Health Impact Blog
From CDC-Authored Genomics Publication Database
This database contains CDC-authored publications in public health genomics including infectious diseases, newborn screening, reproductive health, genetic testing, cancer, chronic diseases, birth defects and developmental disabilities, environmental and occupational health as well as laboratory, bioinformatics and statistical methods.
- Laboratory Investigation of <i>Salmonella enterica</i> serovar Poona Outbreak in California: Comparison of Pulsed-Field Gel Electrophoresis (PFGE) and Whole Genome Sequencing (WGS) Results.
Kozyreva Varvara K et al. PLoS currents 2016 Nov - Use of whole-genome sequencing data to analyze 23S rRNA-mediated azithromycin resistance.
Johnson Steven R et al. International journal of antimicrobial agents 2016 Dec - Universal Human Papillomavirus Typing Assay: Whole Genome Sequencing Following Target Enrichment.
Li Tengguo et al. Journal of clinical microbiology 2016 Dec - Development of a multiplex taqMan real-time PCR assay for typing of Mycoplasma pneumoniae based on type-specific indels identified through whole genome sequencing.
Wolff Bernard J et al. Diagnostic microbiology and infectious disease 2016 Nov - Using whole genome sequencing to identify resistance determinants and predict antimicrobial resistance phenotypes for year 2015 invasive pneumococcal disease isolates recovered in the United States.
Metcalf Benjamin J et al. Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases 2016 Aug
From Guideline Database
This database contains updated guidelines, policies and recommendations on genomic research and practice, as provided by professional organizations, federal advisory groups, expert panels and policy groups.
- Informed consent for whole-genome sequencing studies in the clinical setting. Proposed recommendations on essential content and process.
Published 2013 (Expert panel) - Current issues in medically assisted reproduction and genetics in Europe: research, clinical practice, ethics, legal issues and policy. European Society of Human Genetics and European Society of Human Reproduction and Embryology.
Published 2013 (European Society of Human Genetics) (European Society of Human Reproduction and Embryology) (European Union Eurogentest2 Coordination Action Project) - Whole-genome sequencing in newborn screening? A statement on the continued importance of targeted approaches in newborn screening programmes.
Published 2015 (European Society of Human Genetics ) (P3G International Paediatric Platform) (Human Genome Organisation) (PHG Foundation)
From HuGE Literature Finder Database
This database contains published literature on genetic associations and other human genome epidemiology
- Exploring the genetic architecture of inflammatory bowel disease by whole-genome sequencing identifies association at ADCY7.
Nature genetics 2017 Jan .
Luo Yang, de Lange Katrina M, Jostins Luke, Moutsianas Loukas, Randall Joshua, Kennedy Nicholas A, Lamb Christopher A, McCarthy Shane, Ahmad Tariq, Edwards Cathryn, Serra Eva Goncalves, Hart Ailsa, Hawkey Chris, Mansfield John C, Mowat Craig, Newman William G, Nichols Sam, Pollard Martin, Satsangi Jack, Simmons Alison, Tremelling Mark, Uhlig Holm, Wilson David C, Lee James C, Prescott Natalie J, Lees Charlie W, Mathew Christopher G, Parkes Miles, Barrett Jeffrey C, Anderson Carl - Evaluation of the Myocilin Mutation Gln368Stop Demonstrates Reduced Penetrance for Glaucoma in European Populations.
Ophthalmology 2016 Dec .
Nag Abhishek, Lu Han, Arno Matthew, Iglesias Adriana I, Bonnemaijer Pieter, Broer Linda, Uitterlinden Andre G, Klaver Caroline C W, van Duijn Cornelia, Hysi Pirro G, Hammond Christopher - Mutation load in melanoma is affected by MC1R genotype.
Pigment cell & melanoma research 2016 Dec .
Johansson Peter A, Pritchard Antonia, Patch Ann-Marie, Wilmott James S, Pearson John V, Waddell Nicola, Scolyer Richard A, Mann Graham J, Hayward Nicholas - The Genetic Architecture of Major Depressive Disorder in Han Chinese Women.
JAMA psychiatry 2016 Dec .
Peterson Roseann E, Cai Na, Bigdeli Tim B, Li Yihan, Reimers Mark, Nikulova Anna, Webb Bradley T, Bacanu Silviu-Alin, Riley Brien P, Flint Jonathan, Kendler Kenneth - Genetic variation in the miR-708 gene and its binding targets in bipolar disorder.
Bipolar disorders 2016 Nov .
Fiorentino Alessia, O'Brien Niamh Louise, Sharp Sally Isabel, Curtis David, Bass Nicholas James, McQuillin Andr
.png)
No hay comentarios:
Publicar un comentario