GWAS Central: a comprehensive resource for the discovery and comparison of genotype and phenotype data from genome-wide association studies

por Beck, Tim, Shorter, Tom, Brookes, Anthony J
Publicado 2020

Lower rate of genomic variation identified in the trans-membrane domain of monoamine sub-class of Human G-Protein Coupled Receptors: The Human GPCR-DB Database

por Wahlestedt, Claes, Brookes, Anthony J, Mottagui-Tabar, Salim
Publicado 2004

GWAS Central: an expanding resource for finding and visualising genotype and phenotype data from genome-wide association studies

por Beck, Tim, Rowlands, Thomas, Shorter, Tom, Brookes, Anthony J
Publicado 2022

Data and sample sharing as an enabler for large-scale biomarker research and development: The EPND perspective

por Bose, Niranjan, Brookes, Anthony J., Scordis, Phil, Visser, Pieter Jelle
Publicado 2022

Semantically enabling a genome-wide association study database

por Beck, Tim, Free, Robert C, Thorisson, Gudmundur A, Brookes, Anthony J
Publicado 2012

GWAS Central: a comprehensive resource for the comparison and interrogation of genome-wide association studies

por Beck, Tim, Hastings, Robert K, Gollapudi, Sirisha, Free, Robert C, Brookes, Anthony J
Publicado 2014

VariantValidator: Accurate validation, mapping, and formatting of sequence variation descriptions

por Freeman, Peter J., Hart, Reece K., Gretton, Liam J., Brookes, Anthony J., Dalgleish, Raymond
Publicado 2017

SNPs Meet CNVs in Genome-Wide Association Studies: HGV2007 Meeting Report

por Estivill, Xavier, Cox, Nancy J., Chanock, Stephen J., Kwok, Pui-Yan, Scherer, Stephen W., Brookes, Anthony J.
Publicado 2008

A 129-kb Deletion on Chromosome 12 Confers Substantial Protection Against Rheumatoid Arthritis, Implicating the Gene SLC2A3

por Veal, Colin D, Reekie, Katherine E, Lorentzen, Johnny C, Gregersen, Peter K, Padyukov, Leonid, Brookes, Anthony J
Publicado 2014

HGVbaseG2P: a central genetic association database

por Thorisson, Gudmundur A., Lancaster, Owen, Free, Robert C., Hastings, Robert K., Sarmah, Pallavi, Dash, Debasis, Brahmachari, Samir K., Brookes, Anthony J.
Publicado 2009

Automated design of paralogue ratio test assays for the accurate and rapid typing of copy number variation

por Veal, Colin D., Xu, Hang, Reekie, Katherine, Free, Robert, Hardwick, Robert J., McVey, David, Brookes, Anthony J., Hollox, Edward J., Talbot, Christopher J.
Publicado 2013

Characteristics and longitudinal progression of chronic obstructive pulmonary disease in GOLD B patients

por Lawrence, Philip J., Kolsum, Umme, Gupta, Vandana, Donaldson, Gavin, Singh, Richa, Barker, Bethan, George, Leena, Webb, Adam, Brookes, Anthony J., Brightling, Christopher, Wedzicha, Jadwiga, Singh, Dave
Publicado 2017

Targeted enrichment of genomic DNA regions for next-generation sequencing

por Mertes, Florian, ElSharawy, Abdou, Sauer, Sascha, van Helvoort, Joop M.L.M., van der Zaag, P.J., Franke, Andre, Nilsson, Mats, Lehrach, Hans, Brookes, Anthony J.
Publicado 2011

A mechanistic basis for amplification differences between samples and between genome regions

por Veal, Colin D, Freeman, Peter J, Jacobs, Kevin, Lancaster, Owen, Jamain, Stéphane, Leboyer, Marion, Albanes, Demetrius, Vaghela, Reshma R, Gut, Ivo, Chanock, Stephen J, Brookes, Anthony J
Publicado 2012

Simplifying research access to genomics and health data with Library Cards

por Cabili, Moran N., Carey, Knox, Dyke, Stephanie O. M., Brookes, Anthony J., Fiume, Marc, Jeanson, Francis, Kerry, Giselle, Lash, Alex, Sofia, Heidi, Spalding, Dylan, Tasse, Anne-Marie, Varma, Susheel, Pandya, Ravi
Publicado 2018

Genetic Structures of Copy Number Variants Revealed by Genotyping Single Sperm

por Luo, Minjie, Cui, Xiangfeng, Fredman, David, Brookes, Anthony J., Azaro, Marco A., Greenawalt, Danielle M., Hu, Guohong, Wang, Hui-Yun, Tereshchenko, Irina V., Lin, Yong, Shentu, Yue, Gao, Richeng, Shen, Li, Li, Honghua
Publicado 2009

Data sharing in neurodegenerative disease research: challenges and learnings from the innovative medicines initiative public-private partnership model

por Bradshaw, Angela, Hughes, Nigel, Vallez-Garcia, David, Chokoshvili, Davit, Owens, Andrew, Hansen, Clint, Emmert, Kirsten, Maetzler, Walter, Killin, Lewis, Barnes, Rodrigo, Brookes, Anthony J., Visser, Pieter Jelle, Hofmann-Apitius, Martin, Diaz, Carlos, Steukers, Lennert
Publicado 2023

Blood and sputum eosinophils in COPD; relationship with bacterial load

por Kolsum, Umme, Donaldson, Gavin C., Singh, Richa, Barker, Bethan L., Gupta, Vandana, George, Leena, Webb, Adam J., Thurston, Sarah, Brookes, Anthony J, McHugh, Timothy D., Wedzicha, Jadwiga A., Brightling, Christopher E., Singh, Dave
Publicado 2017

Beacon v2 and Beacon networks: A “lingua franca” for federated data discovery in biomedical genomics, and beyond

por Rambla, Jordi, Baudis, Michael, Ariosa, Roberto, Beck, Tim, Fromont, Lauren A., Navarro, Arcadi, Paloots, Rahel, Rueda, Manuel, Saunders, Gary, Singh, Babita, Spalding, John D., Törnroos, Juha, Vasallo, Claudia, Veal, Colin D., Brookes, Anthony J.
Publicado 2022

A P3G Generic Access Agreement for Population Genomic Studies

por Knoppers, Bartha Maria, Chisholm, Rex L, Kaye, Jane, Cox, David, Thorogood, Adrian, Burton, Paul, Brookes, Anthony J, Fortier, Isabel, Goodwin, Pat, Harris, Jennifer R, Hveem, Kristian, Kent, Alistair, Little, Julian, Riegman, Peter HJ, Ripatti, Samuli, Stolk, Ronald P
Publicado 2013