evs.gs.washington.edu

Exome Variant Server

NHLBI Exome Sequencing Project (ESP). Data Usage and Release. The goal of the NHLBI GO Exome Sequencing Project (ESP). The groups participating and collaborating in the NHLBI GO ESP include:. Seattle GO - University of Washington, Seattle, WA. Broad GO - Broad Institute of MIT and Harvard, Cambridge, MA. WHISP GO - Ohio State University Medical Center, Columbus, OH. Lung GO - University of Washington, Seattle, WA. WashU GO - Washington University, St. Louis, MO. Women's Health Initiative (WHI). COPD Gene...

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NHLBI Exome Sequencing Project (ESP). Data Usage and Release. The goal of the NHLBI GO Exome Sequencing Project (ESP). The groups participating and collaborating in the NHLBI GO ESP include:. Seattle GO - University of Washington, Seattle, WA. Broad GO - Broad Institute of MIT and Harvard, Cambridge, MA. WHISP GO - Ohio State University Medical Center, Columbus, OH. Lung GO - University of Washington, Seattle, WA. WashU GO - Washington University, St. Louis, MO. Women's Health Initiative (WHI). COPD Gene...

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2 data browser

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4 what's new

5 contact and faq

6 downloads

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8 cleveland clinic genebank

9 target

10 gene hugo

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Exome Variant Server | evs.gs.washington.edu Reviews

https://evs.gs.washington.edu

NHLBI Exome Sequencing Project (ESP). Data Usage and Release. The goal of the NHLBI GO Exome Sequencing Project (ESP). The groups participating and collaborating in the NHLBI GO ESP include:. Seattle GO - University of Washington, Seattle, WA. Broad GO - Broad Institute of MIT and Harvard, Cambridge, MA. WHISP GO - Ohio State University Medical Center, Columbus, OH. Lung GO - University of Washington, Seattle, WA. WashU GO - Washington University, St. Louis, MO. Women's Health Initiative (WHI). COPD Gene...

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genome.plantregulome.org

UCSC Genome Browser: News Archives

http://genome.plantregulome.org/goldenPath/newsarch.html

19 December 2014 - New Cow (bosTau8) Assembly Now Available in the Genome Browser. We are pleased to announce the release of a Genome Browser for the June 2014 assembly of cow, Bos taurus. Bos taurus UMD 3.1.1, UCSC version bosTau8). This updated cow assembly was provided by the UMD Center for Bioinformatics and Computational Biology. Bulk downloads of the sequence and annotation data are available via the Genome Browser FTP server. Page These data have specific conditions for use. Dm6) browser annotatio...

gastroenterology.blueprintgenetics.com

Genetic testing for Pancreatitis - Gastroenterology

http://gastroenterology.blueprintgenetics.com/panels/pancreatitis-panel

Blueprint Genetics - Gastroenterology. Ear Nose and Throat. Whole Genome Del/Dup (CNV). Our Sequence Analysis is based on a proprietary targeted sequencing method OS-Seq and offers panels targeted for genes associated with certain phenotypes. A standard way to analyze NGS data for finding the genetic cause for Mendelian disorders. Results in 21 days. Targeted Del/Dup (CNV) analysis is used to detect bigger disease causing deletions or duplications from the disease-associated genes. Results in 21 days.

ajpcell.physiology.org

Nonsynonymous single nucleotide polymorphisms of NHE3 differentially decrease NHE3 transporter activity | Cell Physiology

http://ajpcell.physiology.org/content/308/9/C758

Skip to main content. Other Journals from APS. Search for this keyword. Nonsynonymous single nucleotide polymorphisms of NHE3 differentially decrease NHE3 transporter activity. John R. Horton. American Journal of Physiology - Cell Physiology. Published 1 May 2015. Department of Medicine, Division of Gastroenterology and Hepatology, Center of Cardiovascular Sciences, Albany Medical Center, Albany, New York;. Find this author on Google Scholar. Find this author on PubMed. Search for this author on this site.

droog.gs.washington.edu

Nickerson Lab - Tools and Data

http://droog.gs.washington.edu/datatools.html

Genome Variation Server (GVS). Last update December 2015.

genomena.com

Rare variants, disease, and population size – Genomena

http://genomena.com/genomes-and-health/rare-variants-disease-and-population-size

As genomes evolve, so does the world. Three small steps toward genomically sensible healthcare. Harmful by any other name: On clinical variant classification. The Shock of the New: What we can say about HeLa’s novel variants. Harmful by any other name: On clinical variant classification. Genetics, evolution, and policy. TedMed 2010 Your moderator interprets Ozzy Osbourne’s genome. Really. NOVA: Cracking Your Genetic Code Helping explain the prospect of genomically personalized healthcare. Bolstered by th...

biomedicinahoy.com

Biomedicina Hoy: enero 2013

http://www.biomedicinahoy.com/2013_01_01_archive.html

Biomedicine - Биомедицина - Biomedizin - Biomédecine - الطب الحيوي. Martes, 15 de enero de 2013. Participa como voluntario en Estudios de Biodisponibilidad de fármacos. El Centro de Investigaciones Farmacológicas y Toxicológicas (IFT) de la Universidad de Chile invita a praticipar como voluntario en Estudios de Biodisponibilidad de farmacos. Los estudios se realizan de acuerdo a estrictos controles médicos y éticos y de acuerdo a las normativas nacionales e internacionales. Edad entre 21 y 55 años. Cualq...

growthgenetics.com

The Growth Genetics Consortium

http://www.growthgenetics.com/dispatch.fcgi/c_f/gene/GHRHR

Click anywhere in this box to dismiss it.). Clicking on the arrow adjacent to each ID# will allow access to molecular, clinical and biochemical information concerning this specific gene defect. Is based upon a 5-class system, as described in: Wallis, et al: Practice guidelines for the evaluation of pathogenicity and the reporting of sequence variants in clinical molecular genetics. Approved by the Association of Clinical Genetic science, September, 2013. The minor allele frequency. Submit A New Case.

growthgenetics.com

The Growth Genetics Consortium

http://www.growthgenetics.com/dispatch.fcgi/c_f/gene/GHR

Click anywhere in this box to dismiss it.). Clicking on the arrow adjacent to each ID# will allow access to molecular, clinical and biochemical information concerning this specific gene defect. Is based upon a 5-class system, as described in: Wallis, et al: Practice guidelines for the evaluation of pathogenicity and the reporting of sequence variants in clinical molecular genetics. Approved by the Association of Clinical Genetic science, September, 2013. The minor allele frequency. Submit A New Case.

dnastar.com

DNASTAR- Variant Analysis Software | DNASTAR

http://www.dnastar.com/t-sub-solutions-genome-solutions-snp-analysis.aspx

Protein Sequence and Structure. Metagenomic Assembly with Host Removal. Reference Guided Genome Alignment. 1 in NGS Accuracy. DbNSFP Gene Level Annotations. Variant analysis software provides tools to simplify the discovery and analysis of variants in multiplexed data generated by all major next-gen sequencing platforms including Roche 454. Our variant analysis software enables you to:. Utilize DNASTAR's new human variant annotation database, which bundles together data from dbNSFP. Fluidigm Access Array...

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Dla nauki i rozrywki. Firma EVS Education powstała w 2008 roku. Tworzymy dynamiczny i kreatywny zespół, który przez "edukację" rozumie proces kształcenia własnego umysłu. Jednym z pierwszych projektów firmy było stworzenie wyjątkowej gry planszowej Prime Suspect. Projekt ten spełnia potrzebę, która w czasopiśmie Scientific American Mind. Scientific American Mind 40, 1 (2009): 22-29). Kolejne projekty firmy obejmują rozwój nauki języków obcych z użyciem internetu.

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evs.gs.washington.edu

Exome Variant Server

NHLBI Exome Sequencing Project (ESP). Data Usage and Release. The goal of the NHLBI GO Exome Sequencing Project (ESP). The groups participating and collaborating in the NHLBI GO ESP include:. Seattle GO - University of Washington, Seattle, WA. Broad GO - Broad Institute of MIT and Harvard, Cambridge, MA. WHISP GO - Ohio State University Medical Center, Columbus, OH. Lung GO - University of Washington, Seattle, WA. WashU GO - Washington University, St. Louis, MO. Women's Health Initiative (WHI). COPD Gene...

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IBackup EVS - Encrypted and versioned file system (EVS) - for Online Backup, Sync and more

Design, develop, customize and release secure applications for cloud store. Less Code, Faster Apps. With Command Line utility. Cloud Storage designed with Encryption, Versioning and Block Level Incremental Transfers. We built IBackup on our APIs. You could build your apps too! Our flagship online backup application for small businesses is developed entirely based on the APIs. IBackup supports desktop applications for Windows. And access via iOS platform. To customize, develop, store and access data.

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IDrive EVS - Encrypted and versioned file system (EVS) - for Online Backup, Cloud Storage and more

Design, develop, customize and release secure applications for cloud store. Less Code, Faster Apps. With Command Line utility. Cloud Storage designed with Encryption, Versioning and Block Level Incremental Transfers. We built IDrive on our APIs. You could build your apps too! Our flagship online backup application for consumers and small businesses is developed entirely based on the APIs. IDrive supports desktop applications for Windows. And access via iOS platform. Windows, Mac, Linux).

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