Cargando…

NCBI’s Database of Genotypes and Phenotypes: dbGaP

The Database of Genotypes and Phenotypes (dbGap, http://www.ncbi.nlm.nih.gov/gap) is a National Institutes of Health-sponsored repository charged to archive, curate and distribute information produced by studies investigating the interaction of genotype and phenotype. Information in dbGaP is organiz...

Descripción completa

Detalles Bibliográficos
Autores principales:	Tryka, Kimberly A., Hao, Luning, Sturcke, Anne, Jin, Yumi, Wang, Zhen Y., Ziyabari, Lora, Lee, Moira, Popova, Natalia, Sharopova, Nataliya, Kimura, Masato, Feolo, Michael
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Oxford University Press 2014
Materias:	VI. Genomic variation, diseases and drugs
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3965052/ https://www.ncbi.nlm.nih.gov/pubmed/24297256 http://dx.doi.org/10.1093/nar/gkt1211

Ejemplares similares

DriverDB: an exome sequencing database for cancer driver gene identification
por: Cheng, Wei-Chung, et al.
Publicado: (2014)

Rail-dbGaP: analyzing dbGaP-protected data in the cloud with Amazon Elastic MapReduce
por: Nellore, Abhinav, et al.
Publicado: (2016)

The dbGaP data browser: a new tool for browsing dbGaP controlled-access genomic data
por: Wong, Kira M., et al.
Publicado: (2017)

Precision annotation of digital samples in NCBI’s gene expression omnibus
por: Hadley, Dexter, et al.
Publicado: (2017)

Identifying Datasets for Cross-Study Analysis in dbGaP using PhenX
por: Pan, Huaqin, et al.
Publicado: (2022)

The ChEMBL bioactivity database: an update
por: Bento, A. Patrícia, et al.
Publicado: (2014)

dbGaPCheckup: pre-submission checks of dbGaP-formatted subject phenotype files
por: Heinsberg, Lacey W., et al.
Publicado: (2023)

NCBI’s Virus Discovery Hackathon: Engaging Research Communities to Identify Cloud Infrastructure Requirements
por: Connor, Ryan, et al.
Publicado: (2019)

canSAR: updated cancer research and drug discovery knowledgebase
por: Bulusu, Krishna C., et al.
Publicado: (2014)

Therapeutic target database update 2014: a resource for targeted therapeutics
por: Qin, Chu, et al.
Publicado: (2014)

rSNPBase: a database for curated regulatory SNPs
por: Guo, Liyuan, et al.
Publicado: (2014)

CAMP: Collection of sequences and structures of antimicrobial peptides
por: Waghu, Faiza Hanif, et al.
Publicado: (2014)

HMDD v2.0: a database for experimentally supported human microRNA and disease associations
por: Li, Yang, et al.
Publicado: (2014)

NECTAR: a database of codon-centric missense variant annotations
por: Gong, Sungsam, et al.
Publicado: (2014)

The IUPHAR/BPS Guide to PHARMACOLOGY: an expert-driven knowledgebase of drug targets and their ligands
por: Pawson, Adam J., et al.
Publicado: (2014)

DECIPHER: database for the interpretation of phenotype-linked plausibly pathogenic sequence and copy-number variation
por: Bragin, Eugene, et al.
Publicado: (2014)

The Database of Genomic Variants: a curated collection of structural variation in the human genome
por: MacDonald, Jeffrey R., et al.
Publicado: (2014)

Progenetix: 12 years of oncogenomic data curation
por: Cai, Haoyang, et al.
Publicado: (2014)

The Human Phenotype Ontology project: linking molecular biology and disease through phenotype data
por: Köhler, Sebastian, et al.
Publicado: (2014)

DrugBank 4.0: shedding new light on drug metabolism
por: Law, Vivian, et al.
Publicado: (2014)

The Transformer database: biotransformation of xenobiotics
por: Hoffmann, Michael F., et al.
Publicado: (2014)

InvFEST, a database integrating information of polymorphic inversions in the human genome
por: Martínez-Fundichely, Alexander, et al.
Publicado: (2014)

The NHGRI GWAS Catalog, a curated resource of SNP-trait associations
por: Welter, Danielle, et al.
Publicado: (2014)

Developments in FINDbase worldwide database for clinically relevant genomic variation allele frequencies
por: Papadopoulos, Petros, et al.
Publicado: (2014)

bNAber: database of broadly neutralizing HIV antibodies
por: Eroshkin, Alexey M., et al.
Publicado: (2014)

SuperPain—a resource on pain-relieving compounds targeting ion channels
por: Gohlke, Björn O., et al.
Publicado: (2014)

AVPdb: a database of experimentally validated antiviral peptides targeting medically important viruses
por: Qureshi, Abid, et al.
Publicado: (2014)

Updates on the web-based VIOLIN vaccine database and analysis system
por: He, Yongqun, et al.
Publicado: (2014)

Updates of the HbVar database of human hemoglobin variants and thalassemia mutations
por: Giardine, Belinda, et al.
Publicado: (2014)

PubChem BioAssay: 2014 update
por: Wang, Yanli, et al.
Publicado: (2014)

ClinVar: public archive of relationships among sequence variation and human phenotype
por: Landrum, Melissa J., et al.
Publicado: (2014)

Lynx: a database and knowledge extraction engine for integrative medicine
por: Sulakhe, Dinanath, et al.
Publicado: (2014)

SAbDab: the structural antibody database
por: Dunbar, James, et al.
Publicado: (2014)

The NEI/NCBI dbGAP database: Genotypes and haplotypes that may specifically predispose to risk of neovascular age-related macular degeneration
por: Zhang, Hong, et al.
Publicado: (2008)

NCBI’s Virus Discovery Codeathon: Building “FIVE” —The Federated Index of Viral Experiments API Index
por: Martí-Carreras, Joan, et al.
Publicado: (2020)

Precise diagnosis of three top cancers using dbGaP data
por: Liu, Xu-Qing, et al.
Publicado: (2021)

Extending TCGA queries to automatically identify analogous genomic data from dbGaP
por: Wagner, Erin K., et al.
Publicado: (2017)

“METAGENOTE: a simplified web platform for metadata annotation of genomic samples and streamlined submission to NCBI’s sequence read archive”
por: Quiñones, Mariam, et al.
Publicado: (2020)

Briefing session - International Day of Women and Girls in Science
por: Bouvier, Marie Beatrice, et al.
Publicado: (2019)

Conférence pour les guides CERN
por: Rossi, Lucio
Publicado: (2019)

Cannot write session to /tmp/vufind_sessions/sess_lvf6q4httpefpv7k3s1cd69ng0