gwascentral.org

GWAS Central - Home

Enter a study id, dbSNP id, MeSH/HPO phenotype term, keywords, author names, HGNC gene symbols, chromosomal regions or PUBMED identifier. GWAS Central provides a centralized compilation of summary level findings from genetic association studies, both large and small. We actively gather datasets from public domain projects, and encourage direct data submission from the community. See more. Use GWAS Central as a data source. GWAS Central data release November 2017 Read more.

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GWAS Central - Home | gwascentral.org Reviews

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Enter a study id, dbSNP id, MeSH/HPO phenotype term, keywords, author names, HGNC gene symbols, chromosomal regions or PUBMED identifier. GWAS Central provides a centralized compilation of summary level findings from genetic association studies, both large and small. We actively gather datasets from public domain projects, and encourage direct data submission from the community. See more. Use GWAS Central as a data source. GWAS Central data release November 2017 Read more.

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GWAS Central - Home | gwascentral.org Reviews

https://gwascentral.org

Enter a study id, dbSNP id, MeSH/HPO phenotype term, keywords, author names, HGNC gene symbols, chromosomal regions or PUBMED identifier. GWAS Central provides a centralized compilation of summary level findings from genetic association studies, both large and small. We actively gather datasets from public domain projects, and encourage direct data submission from the community. See more. Use GWAS Central as a data source. GWAS Central data release November 2017 Read more.

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gwascentral.org

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GWAS Central - Studies

https://www.gwascentral.org/studies

Search studies using keywords. Enter study ID, authors, pubmed ID, other terms. Log p ≥ 0. Log p ≥ 1. Log p ≥ 2. Log p ≥ 3. Log p ≥ 4. Log p ≥ 5. Log p ≥ 6. Log p ≥ 7. Log p ≥ 8. Log p ≥ 9. Log p ≥ 10. Studies in the database containing data with -log p ≥ 0. Number of markers (ascending). Number of markers (descending). Export these results as. Choose a format -. Choose a canned query-. Retrieve p-values for studies. Retrieve genes for studies. Add data sets to Browser. GWAS of Sleep latency. Amin N et al.

2

GWAS Central - Browser

https://www.gwascentral.org/browser

Use the Browser to integrate and interrogate data sets graphically. To add new data to the Browser use the Studies. Or upload your own data sets using the Upload. You have not added any Studies or Phenotypes or uploaded any data sets.

3

GWAS Central - Markers

https://www.gwascentral.org/markers

Search markers using identifiers. Enter dbSNP rsID/GWAS Central IDs (space separated). Log p ≥ 0. Log p ≥ 1. Log p ≥ 2. Log p ≥ 3. Log p ≥ 4. Log p ≥ 5. Log p ≥ 6. Log p ≥ 7. Log p ≥ 8. Log p ≥ 9. Log p ≥ 10. With associations above threshold.

4

GWAS Central - Phenotypes

https://www.gwascentral.org/phenotypes/tree

Using a MeSH/HPO term. By browsing phenotype trees. Medical Subject Headings (MeSH). Human Phenotype Ontology (HPO). Only the MeSH headings used in the annotation of phenotypes are displayed. The numbers refer to the number of study phenotype methods annotated to that heading (at zero threshold) and all child headings where they exist. The "OR" search operator is used when multiple headings are checked. Collapse tree and uncheck all. Created by U.S. National Library of Medicine.

5

GWAS Central - Home

https://www.gwascentral.org/index

Enter a study id, dbSNP id, MeSH/HPO phenotype term, keywords, author names, HGNC gene symbols, chromosomal regions or PUBMED identifier. GWAS Central provides a centralized compilation of summary level findings from genetic association studies, both large and small. We actively gather datasets from public domain projects, and encourage direct data submission from the community. See more. Use GWAS Central as a data source. GWAS Central data release January 2016 Read more.

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toppgene.cchmc.org

Links

https://toppgene.cchmc.org/navigation/links.jsp

A one-stop portal for gene list enrichment analysis and candidate gene prioritization. Based on functional annotations and protein interactions network. ToppGene Suite would not be possible without the efforts and contributions to the scientific community of the following institutions. A database for gene annotations. European Molecular Biology Laboratory. The Gene Ontology project provides a controlled vocabulary to describe gene and gene product attributes in any organism. GWAS Central (previously the ...

humanas.org.ar

Fundación Humanas | Sitios de Interés

http://humanas.org.ar/sitios-de-interes

Cine y Salud Mental. 8211; Quiénes somos? 8211; Atención Profesional. 8211; Cómo llegar? 8211; Cursos y Carreras. 8211; Cine y Salud Mental. 8211; Medicina Familiar. 8211; Consultorios Externos. National Human Genome Research Institute. National Institutes of Health. Organización Mundial de la Salud. Organización Panamericana de la Salud. Academia Nacional de Medicina. Biblioteca Virtual de Salud y Desastres. Nature Precedings: Pre-publication Research and Preliminary Findings. The Whole Brain Atlas.

genenames.org

All links | HUGO Gene Nomenclature Committee

http://www.genenames.org/useful/all-links

Use * to search with a root symbol (eg ZNF*). Old gene families archive. Statistics and downloads help. Genome Databases and Browsers. Human Genome Databases, Browsers and Variation Resources. Other Vertebrate Genome Databases and Browsers. Non-Vertebrate Genome Databases and Browsers. Orthology and Comparative Genomics Resources. Other gene and nucleic acid resources. General gene and nucleic acid resources. Genome Databases and Browsers. Human Genome Databases, Browsers and Variation Resources. A commu...

hildeschjerven.net

HildeSchjerven.net - Links

http://www.hildeschjerven.net/links.html

A list of links to external useful websites are provided for your convenience. HHMI Educational pages (biointeractive page). Public Broadcasting Services. They provide free educational resources. The official website for the Nobel Prize. To search for published scientific papers listed in the NCBI PubMed library. National Institute of Health. The USA national medical research agency with on-site research and funding programs. Web-bases software for primer design. ENCODE (Official NIH link). Free access D...

gwas.biosciencedbc.jp

HLA Database

http://gwas.biosciencedbc.jp/cgi-bin/hladb/hla_top.cgi

HGVRD data sharing policy. National Institute of Genetics. University of Tokyo Hospital. CRL, Hitachi, LTD. This HLA database (HLA DB) is a repository system and has been constructed to achieve permanent data management and information sharing of HLA data. HLA-DB contains HLA haplotype data and disease-related information. We greatly appreciate your HLA data submission. This work has been supported by the Ministry of Education, Culture, Sports, Science and Technology. Multiple alignment Japanese Haplotype.

gwas.biosciencedbc.jp

Human Variation Database

http://gwas.biosciencedbc.jp/cgi-bin/hvdb/hv_top.cgi

About Human Variation DB. HGVRD data sharing policy. National Institute of Genetics. University of Tokyo Hospital. CRL, Hitachi, LTD. About Human genome variation database. This work has been supported by the Japan science and Technology Agency. Search by gene name. Search by disease name. Search by genomic position. Search by SNP number. Browse by disease name. Browse by gene name. Overview of SNP density. Summary of all diseases.

gwas.biosciencedbc.jp

Case Control GWAS (Genome Wide Association Study) Database

http://gwas.biosciencedbc.jp/cgi-bin/gwasdb/gwas_top.cgi

HGVRD data sharing policy. National Institute of Genetics. University of Tokyo Hospital. CRL, Hitachi, LTD. About Case Control GWAS Database. This work has been supported by the Ministry of Education, Culture, Sports, Science and Technology. Case control GWAS search. Browse GWAS results from disease name list. Disease related gene list.

gwas.biosciencedbc.jp

SNP control database

http://gwas.biosciencedbc.jp/snpdb/snp_top.php

About SNP Control DB. HGVRD data sharing policy. National Institute of Genetics. University of Tokyo Hospital. CRL, Hitachi, LTD. About SNP Control Database.

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GWAS Central - Home

Enter a study id, dbSNP id, MeSH/HPO phenotype term, keywords, author names, HGNC gene symbols, chromosomal regions or PUBMED identifier. GWAS Central provides a centralized compilation of summary level findings from genetic association studies, both large and small. We actively gather datasets from public domain projects, and encourage direct data submission from the community. See more. How do I find phenotypes of interest? How do I find genes/regions of interest? How do I find markers of interest?

gwascentral.org

GWAS Central - Home

Enter a study id, dbSNP id, MeSH/HPO phenotype term, keywords, author names, HGNC gene symbols, chromosomal regions or PUBMED identifier. GWAS Central provides a centralized compilation of summary level findings from genetic association studies, both large and small. We actively gather datasets from public domain projects, and encourage direct data submission from the community. See more. Use GWAS Central as a data source. GWAS Central data release November 2017 Read more.

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