GWAS Central
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GWAS Central
metasource: Fairsharing.org
version: FAIRsharing.org: GWAS Central; GWAS Central; DOI: https://doi.org/10.25504/FAIRsharing.vkr57k; Last edited: June 15, 2021, 1:42 p.m.; Last accessed: Jan 03 2022 7:08 p.m.
metasource: bio.tools
version: extracted_at: 2022-11-04T11:29:47.117686
GWAS_Central
metasource: bio.tools
version: extracted_at: 2022-11-04T11:29:47.117686
Names
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GWAS Central
metasource: Fairsharing.orgversion: FAIRsharing.org: GWAS Central; GWAS Central; DOI: https://doi.org/10.25504/FAIRsharing.vkr57k; Last edited: June 15, 2021, 1:42 p.m.; Last accessed: Jan 03 2022 7:08 p.m.
metasource: bio.tools
version: extracted_at: 2022-11-04T11:29:47.117686
GWAS_Central
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:29:47.117686
Names
More detailed information about this field from each metasource.
GWAS Central
metasource: Fairsharing.orgversion: FAIRsharing.org: GWAS Central; GWAS Central; DOI: https://doi.org/10.25504/FAIRsharing.vkr57k; Last edited: June 15, 2021, 1:42 p.m.; Last accessed: Jan 03 2022 7:08 p.m.
metasource: bio.tools
version: extracted_at: 2022-11-04T11:29:47.117686
GWAS_Central
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:29:47.117686
GWAS Central stores genome-wide association study data. The database content comprises direct submissions received from GWAS authors and consortia in addition to actively gathered data sets from various public sources. GWAS data are discoverable from the perspective of genetic markers, genes, genome regions or phenotypes, via graphical visualizations and detailed downloadable data reports.
Description
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GWAS Central stores genome-wide association study data. The database content comprises direct submissions received from GWAS authors and consortia in addition to actively gathered data sets from various public sources. GWAS data are discoverable from the perspective of genetic markers, genes, genome regions or phenotypes, via graphical visualizations and detailed downloadable data reports.
metasource: Fairsharing.orgversion: FAIRsharing.org: GWAS Central; GWAS Central; DOI: https://doi.org/10.25504/FAIRsharing.vkr57k; Last edited: June 15, 2021, 1:42 p.m.; Last accessed: Jan 03 2022 7:08 p.m.
a comprehensive resource for the discovery and comparison of genotype and phenotype data from genome-wide association studies. A database for human genetic variants identified by genome-wide association studies. Enter a study id, dbSNP id, MeSH/HPO phenotype term, keywords, author names, HGNC gene symbols, chromosomal regions or PUBMED identifier. The NHGRI-EBI GWAS Catalog: a curated collection of all published genome-wide association studies, produced by a collaboration between EMBL-EBI and NHGRI. GWAS CENTRAL - INDIA : A Genotype - Phenotype Association Database. GWAS Central - India (previously the Human Genome Variation database of Genotype-to-Phenotype information) is a database of summary level findings from genetic association studies, both large and small. GWAS Central provides a complete Study metadata file for use in data citation research, tracking researcher contributions, data discovery projects, etc
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:29:47.117686
Webpage:
https://www.gwascentral.org/Webpage
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https://www.gwascentral.org/
metasource: Fairsharing.orgversion: FAIRsharing.org: GWAS Central; GWAS Central; DOI: https://doi.org/10.25504/FAIRsharing.vkr57k; Last edited: June 15, 2021, 1:42 p.m.; Last accessed: Jan 03 2022 7:08 p.m.
https://www.gwascentral.org
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:29:47.117686
Licence:
Name: GWAS Central DisclaimerLicence name
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GWAS Central Disclaimer
metasource: Fairsharing.orgversion: FAIRsharing.org: GWAS Central; GWAS Central; DOI: https://doi.org/10.25504/FAIRsharing.vkr57k; Last edited: June 15, 2021, 1:42 p.m.; Last accessed: Jan 03 2022 7:08 p.m.
Licence URL
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https://help.gwascentral.org/disclaimer/
metasource: Fairsharing.orgversion: FAIRsharing.org: GWAS Central; GWAS Central; DOI: https://doi.org/10.25504/FAIRsharing.vkr57k; Last edited: June 15, 2021, 1:42 p.m.; Last accessed: Jan 03 2022 7:08 p.m.
Publications:
Publications
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HGVbaseG2P: a central genetic association database
PMID: 18948288
metasource: Fairsharing.org
version: FAIRsharing.org: GWAS Central; GWAS Central; DOI: https://doi.org/10.25504/FAIRsharing.vkr57k; Last edited: June 15, 2021, 1:42 p.m.; Last accessed: Jan 03 2022 7:08 p.m.
GWAS Central: a comprehensive resource for the discovery and comparison of genotype and phenotype data from genome-wide association studies
PMID: 31612961
metasource: Fairsharing.org
version: FAIRsharing.org: GWAS Central; GWAS Central; DOI: https://doi.org/10.25504/FAIRsharing.vkr57k; Last edited: June 15, 2021, 1:42 p.m.; Last accessed: Jan 03 2022 7:08 p.m.
metasource: bio.tools
version: extracted_at: 2022-11-04T11:29:47.117686
Publications
More detailed information about this field from each metasource.
HGVbaseG2P: a central genetic association database
PMID: 18948288
metasource: Fairsharing.org
version: FAIRsharing.org: GWAS Central; GWAS Central; DOI: https://doi.org/10.25504/FAIRsharing.vkr57k; Last edited: June 15, 2021, 1:42 p.m.; Last accessed: Jan 03 2022 7:08 p.m.
GWAS Central: a comprehensive resource for the discovery and comparison of genotype and phenotype data from genome-wide association studies
PMID: 31612961
metasource: Fairsharing.org
version: FAIRsharing.org: GWAS Central; GWAS Central; DOI: https://doi.org/10.25504/FAIRsharing.vkr57k; Last edited: June 15, 2021, 1:42 p.m.; Last accessed: Jan 03 2022 7:08 p.m.
metasource: bio.tools
version: extracted_at: 2022-11-04T11:29:47.117686
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HGVbaseG2P: a central genetic association database
PubMed citations: 37.
37 articles citing: HGVbaseG2P: a central genetic association database
MAGPEL: an autoMated pipeline for inferring vAriant-driven Gene PanEls from the full-length biomedical literature. PMID:32703994
eGARD: Extracting associations between genomic anomalies and drug responses from text. PMID:29261751
DiMeX: A Text Mining System for Mutation-Disease Association Extraction. PMID:27073839
Genetic Variation in the Human SORBS1 Gene is Associated With Blood Pressure Regulation and Age at Onset of Hypertension: A SAPPHIRe Cohort Study. PMID:26962801
Primary Immunodeficiencies and Inflammatory Disease: A Growing Genetic Intersection. PMID:26791050
Genetic polymorphisms of PCSK2 are associated with glucose homeostasis and progression to type 2 diabetes in a Chinese population. PMID:26607656
Transcriptomic identification of ADH1B as a novel candidate gene for obesity and insulin resistance in human adipose tissue in Mexican Americans from the Veterans Administration Genetic Epidemiology Study (VAGES). PMID:25830378
Personal genomes, participatory genomics and the anonymity-privacy conundrum. PMID:25572254
Hybrid curation of gene-mutation relations combining automated extraction and crowdsourcing. PMID:25246425
The ontology of genetic susceptibility factors (OGSF) and its application in modeling genetic susceptibility to vaccine adverse events. PMID:24963371
GRASP: analysis of genotype-phenotype results from 1390 genome-wide association studies and corresponding open access database. PMID:24931982
LincSNP: a database of linking disease-associated SNPs to human large intergenic non-coding RNAs. PMID:24885522
Worm variation made accessible: Take your shopping cart to store, link, and investigate! PMID:24843834
GWAS Central: a comprehensive resource for the comparison and interrogation of genome-wide association studies. PMID:24301061
WormQTLHD--a web database for linking human disease to natural variation data in C. elegans. PMID:24217915
RAvariome: a genetic risk variants database for rheumatoid arthritis based on assessment of reproducibility between or within human populations. PMID:24158836
Prediction of disease causing non-synonymous SNPs by the Artificial Neural Network Predictor NetDiseaseSNP. PMID:23935863
The GenoChip: a new tool for genetic anthropology. PMID:23666864
Single nucleotide polymorphisms in Mycobacterium tuberculosis and the need for a curated database. PMID:23266261
Semantically enabling a genome-wide association study database. PMID:23244533
The 2013 Nucleic Acids Research Database Issue and the online molecular biology database collection. PMID:23203983
Phenotypic overlap in the contribution of individual genes to CNV pathogenicity revealed by cross-species computational analysis of single-gene mutations in humans, mice and zebrafish. PMID:23104991
Introducing the medical bioinformatics in Journal of Translational Medicine. PMID:23013487
MSV3d: database of human MisSense Variants mapped to 3D protein structure. PMID:22491796
UASIS: Universal Automatic SNP Identification System. PMID:22369494
Target selection for structural genomics based on combining fold recognition and crystallisation prediction methods: application to the human proteome. PMID:22354707
AnnotCompute: annotation-based exploration and meta-analysis of genomics experiments. PMID:22190598
GWASdb: a database for human genetic variants identified by genome-wide association studies. PMID:22139925
DistiLD Database: diseases and traits in linkage disequilibrium blocks. PMID:22058129
Assessing and managing risk when sharing aggregate genetic variant data. PMID:21921928
The case for locus-specific databases. PMID:21540879
The MOLGENIS toolkit: rapid prototyping of biosoftware at the push of a button. PMID:21210979
IGVBrowser--a genomic variation resource from diverse Indian populations. PMID:20843867
Varietas: a functional variation database portal. PMID:20671203
Phenotype ontologies for mouse and man: bridging the semantic gap. PMID:20427557
Models for financial sustainability of biological databases and resources. PMID:20157490
Improved mutation tagging with gene identifiers applied to membrane protein stability prediction. PMID:19758467 -
GWAS Central: a comprehensive resource for the discovery and comparison of genotype and phenotype data from genome-wide association studies
PubMed citations: 22.
22 articles citing: GWAS Central: a comprehensive resource for the discovery and comparison of genotype and phenotype data from genome-wide association studies
Artificial intelligence and machine-learning approaches in structure and ligand-based discovery of drugs affecting central nervous system. PMID:35819579
StarGazer: A Hybrid Intelligence Platform for Drug Target Prioritization and Digital Drug Repositioning Using Streamlit. PMID:35711912
PiER: web-based facilities tailored for genetic target prioritisation harnessing human disease genetics, functional genomics and protein interactions. PMID:35610036
Deep phenotyping: symptom annotation made simple with SAMS. PMID:35524573
Diseases 2.0: a weekly updated database of disease-gene associations from text mining and data integration. PMID:35348648
Auto-CORPus: A Natural Language Processing Tool for Standardizing and Reusing Biomedical Literature. PMID:35243479
Metabolomics and the Multi-Omics View of Cancer. PMID:35208228
STAT3-mediated allelic imbalance of novel genetic variant Rs1047643 and B-cell-specific super-enhancer in association with systemic lupus erythematosus. PMID:35188103
Genetic Determinants of Plasma Low-Density Lipoprotein Cholesterol Levels: Monogenicity, Polygenicity, and "Missing" Heritability. PMID:34829957
A spotter's guide to SNPtic exons: The common splice variants underlying some SNP-phenotype correlations. PMID:34708937
Recent innovations and in-depth aspects of post-genome wide association study (Post-GWAS) to understand the genetic basis of complex phenotypes. PMID:34689168
Knowledge Representation and Management: Interest in New Solutions for Ontology Curation. PMID:34479390
Intra-Ramanome Correlation Analysis Unveils Metabolite Conversion Network from an Isogenic Population of Cells. PMID:34465024
Seeing the forest through the trees: prioritising potentially functional interactions from Hi-C. PMID:34454581
Joint disease-specificity at the regulatory base-pair level. PMID:34230488
Novel susceptibility loci identified in a genome-wide association study of type 2 diabetes complications in population of Latvia. PMID:33430853
PheLiGe: an interactive database of billions of human genotype-phenotype associations. PMID:33245779
LincSNP 3.0: an updated database for linking functional variants to human long non-coding RNAs, circular RNAs and their regulatory elements. PMID:33219661
Data-Driven Modeling of Knowledge Assemblies in Understanding Comorbidity Between Type 2 Diabetes Mellitus and Alzheimer's Disease. PMID:32925069
The Dawn of the Age of Multi-Parent MAGIC Populations in Plant Breeding: Novel Powerful Next-Generation Resources for Genetic Analysis and Selection of Recombinant Elite Material. PMID:32824319
Multi-layered epigenetic regulation of IRS2 expression in the liver of obese individuals with type 2 diabetes. PMID:32710190
The 27th annual Nucleic Acids Research database issue and molecular biology database collection. PMID:31906604
Tags:
Tags
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gene
metasource: Fairsharing.org
version: FAIRsharing.org: GWAS Central; GWAS Central; DOI: https://doi.org/10.25504/FAIRsharing.vkr57k; Last edited: June 15, 2021, 1:42 p.m.; Last accessed: Jan 03 2022 7:08 p.m.
genetic marker
metasource: Fairsharing.org
version: FAIRsharing.org: GWAS Central; GWAS Central; DOI: https://doi.org/10.25504/FAIRsharing.vkr57k; Last edited: June 15, 2021, 1:42 p.m.; Last accessed: Jan 03 2022 7:08 p.m.
genome-wide association study
metasource: Fairsharing.org
version: FAIRsharing.org: GWAS Central; GWAS Central; DOI: https://doi.org/10.25504/FAIRsharing.vkr57k; Last edited: June 15, 2021, 1:42 p.m.; Last accessed: Jan 03 2022 7:08 p.m.
genotype
metasource: Fairsharing.org
version: FAIRsharing.org: GWAS Central; GWAS Central; DOI: https://doi.org/10.25504/FAIRsharing.vkr57k; Last edited: June 15, 2021, 1:42 p.m.; Last accessed: Jan 03 2022 7:08 p.m.
phenotype
metasource: Fairsharing.org
version: FAIRsharing.org: GWAS Central; GWAS Central; DOI: https://doi.org/10.25504/FAIRsharing.vkr57k; Last edited: June 15, 2021, 1:42 p.m.; Last accessed: Jan 03 2022 7:08 p.m.
gwas study
metasource: bio.tools
version: extracted_at: 2022-11-04T11:29:47.117686
genotype and phenotype
metasource: bio.tools
version: extracted_at: 2022-11-04T11:29:47.117686
human genetics
metasource: bio.tools
version: extracted_at: 2022-11-04T11:29:47.117686
dna polymorphism
metasource: bio.tools
version: extracted_at: 2022-11-04T11:29:47.117686
mapping
metasource: bio.tools
version: extracted_at: 2022-11-04T11:29:47.117686
Tags
More detailed information about this field from each metasource.
gene
metasource: Fairsharing.orgversion: FAIRsharing.org: GWAS Central; GWAS Central; DOI: https://doi.org/10.25504/FAIRsharing.vkr57k; Last edited: June 15, 2021, 1:42 p.m.; Last accessed: Jan 03 2022 7:08 p.m.
genetic marker
metasource: Fairsharing.orgversion: FAIRsharing.org: GWAS Central; GWAS Central; DOI: https://doi.org/10.25504/FAIRsharing.vkr57k; Last edited: June 15, 2021, 1:42 p.m.; Last accessed: Jan 03 2022 7:08 p.m.
genome-wide association study
metasource: Fairsharing.orgversion: FAIRsharing.org: GWAS Central; GWAS Central; DOI: https://doi.org/10.25504/FAIRsharing.vkr57k; Last edited: June 15, 2021, 1:42 p.m.; Last accessed: Jan 03 2022 7:08 p.m.
genotype
metasource: Fairsharing.orgversion: FAIRsharing.org: GWAS Central; GWAS Central; DOI: https://doi.org/10.25504/FAIRsharing.vkr57k; Last edited: June 15, 2021, 1:42 p.m.; Last accessed: Jan 03 2022 7:08 p.m.
phenotype
metasource: Fairsharing.orgversion: FAIRsharing.org: GWAS Central; GWAS Central; DOI: https://doi.org/10.25504/FAIRsharing.vkr57k; Last edited: June 15, 2021, 1:42 p.m.; Last accessed: Jan 03 2022 7:08 p.m.
gwas study
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:29:47.117686
genotype and phenotype
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:29:47.117686
human genetics
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:29:47.117686
dna polymorphism
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:29:47.117686
mapping
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:29:47.117686
gene genetic marker genome-wide association study genotype phenotype gwas study genotype and phenotype human genetics dna polymorphism mapping
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