phewas.mc.vanderbilt.edu

PheWAS

Phenome-wide association studies (PheWAS). Analyze many phenotypes compared to a single genetic variant (or other attribute). This method was originally described using electronic medical record (EMR) data from EMR-linked in the Vanderbilt DNA biobank, BioVU, but can also be applied to other richly phenotyped sets. The PheWAS catalog contains the PheWAS results for 3,144 single-nucleotide polymorphisms (SNPs) present in the NHGRI GWAS Catalog. View the PheWAS Catalog. More Information on PheWAS. Denny JC...

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PheWAS | phewas.mc.vanderbilt.edu Reviews

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Phenome-wide association studies (PheWAS). Analyze many phenotypes compared to a single genetic variant (or other attribute). This method was originally described using electronic medical record (EMR) data from EMR-linked in the Vanderbilt DNA biobank, BioVU, but can also be applied to other richly phenotyped sets. The PheWAS catalog contains the PheWAS results for 3,144 single-nucleotide polymorphisms (SNPs) present in the NHGRI GWAS Catalog. View the PheWAS Catalog. More Information on PheWAS. Denny JC...

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PheWAS | phewas.mc.vanderbilt.edu Reviews

https://phewas.mc.vanderbilt.edu

Phenome-wide association studies (PheWAS). Analyze many phenotypes compared to a single genetic variant (or other attribute). This method was originally described using electronic medical record (EMR) data from EMR-linked in the Vanderbilt DNA biobank, BioVU, but can also be applied to other richly phenotyped sets. The PheWAS catalog contains the PheWAS results for 3,144 single-nucleotide polymorphisms (SNPs) present in the NHGRI GWAS Catalog. View the PheWAS Catalog. More Information on PheWAS. Denny JC...

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PheWAS - Phenome Wide Association Studies

https://phewas.mc.vanderbilt.edu/datatable

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PheWAS - Phenome Wide Association Studies

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phekb.org

Resources | PheKB

https://www.phekb.org/resources

Skip to main content. Tips for using PheKB. Public Phenotypes- Phenotypes that are finalized (status set to Final), and are ready to be shared publically. Often these phenotypes have associated publications to them. Phenotypes in development, testing, or validation stages are not viewable publically and can only be viewed when a user is logged and the phenotype has been shared with the user via a Collaborative group. How to Use PheKB. How to Share Phenotypes on PheKB. How to Share Data on PheKB. Is avail...

genetrail2.bioinf.uni-sb.de

GeneTrail2

http://genetrail2.bioinf.uni-sb.de/start.html

Https:/ genetrail2.bioinf.uni-sb.de. Https:/ regulatortrail.bioinf.uni-sb.de. Ötzi the Iceman (ORA). Integrative / Comparative analysis. Wilms' tumors (mRNA miRNA). Statistical analysis of molecular signatures. Please insert your username or email address. Data and perform enrichment analysis based on gene sets derived from popular databases like GO. Data and perform enrichment analysis based on protein datasets like SMPDB. Or map proteins to corresponding genes and perform a gene set analysis.

emerge.mc.vanderbilt.edu

welcome to eMerge > Collaborate

https://emerge.mc.vanderbilt.edu/index.php

Number of network publications. Number of phenotypes developed. Number of participants in the Network Cohort. EMERGE is a national network organized and funded by the National Human Genome Research Institute (NHGRI) that combines DNA biorepositories with electronic medical record (EMR) systems for large scale, high-throughput genetic research in support of implementing genomic medicine. Popular tools (click on a button below). Addiction biology. 2016 Nov;21(6):1217-1232. To view a list of eMERGE-specific...

emerge.mc.vanderbilt.edu

welcome to eMerge

https://emerge.mc.vanderbilt.edu/index.php?page_id=244

Number of network publications. Number of phenotypes developed. Number of participants in the Network Cohort. EMERGE Representation at ASHG 2016 in Vancouver, British Columbia, Canada. October 18, 2016 - 01:43PM - by kaylamhowell. Safe travels to our eMERGE investigators as they head to Vancouver this week to participate in ASHG 2016. Click here. To view a list of eMERGE-specific presentations and here. For general eMERGE representation. For more information about ASHG 2016, click here. PheKB is a collab...

pic-sure.org

Blog & News | PIC-SURE

http://pic-sure.org/blog

Skip to main content. Patient-centered Information Commons: Standardized Unification of Research Elements. A BD2K Center of Excellence. Nine-Week Summer Institute for Undergrads Now Accepting Applications. January 5, 2017. April 15, 2016. John Brownstein described various new modes of data acquisition. FeverPrint iOS app to understand baseline temperature over large populations: https:/ itunes.apple.com/us/app/feverprints-study-about-body/id108741198. Read more about Digital Phenotype. New Big Data Tools.

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phewas.mc.vanderbilt.edu

PheWAS

Phenome-wide association studies (PheWAS). Analyze many phenotypes compared to a single genetic variant (or other attribute). This method was originally described using electronic medical record (EMR) data from EMR-linked in the Vanderbilt DNA biobank, BioVU, but can also be applied to other richly phenotyped sets. The PheWAS catalog contains the PheWAS results for 3,144 single-nucleotide polymorphisms (SNPs) present in the NHGRI GWAS Catalog. View the PheWAS Catalog. More Information on PheWAS. Denny JC...

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