Tracking human population structure through time from whole genome sequences

por Wang, Ke, Mathieson, Iain, O’Connell, Jared, Schiffels, Stephan
Publicado 2020

NxRepair: error correction in de novo sequence assembly using Nextera mate pairs

por Murphy, Rebecca R., O’Connell, Jared, Cox, Anthony J., Schulz-Trieglaff, Ole
Publicado 2015

Nuclear genome-wide associations with mitochondrial heteroplasmy

por Nandakumar, Priyanka, Tian, Chao, O’Connell, Jared, Hinds, David, Paterson, Andrew D., Sondheimer, Neal
Publicado 2021

Haplotype estimation for biobank scale datasets

por O’Connell, Jared, Sharp, Kevin, Shrine, Nick, Wain, Louise, Hall, Ian, Tobin, Martin, Zagury, Jean-Francois, Delaneau, Olivier, Marchini, Jonathan
Publicado 2016

An Ensemble Penalized Regression Method for Multi-ancestry Polygenic Risk Prediction

por Zhang, Jingning, Zhan, Jianan, Jin, Jin, Ma, Cheng, Zhao, Ruzhang, O’ Connell, Jared, Jiang, Yunxuan, Koelsch, Bertram L., Zhang, Haoyu, Chatterjee, Nilanjan
Publicado 2023

A population-specific reference panel for improved genotype imputation in African Americans

por O’Connell, Jared, Yun, Taedong, Moreno, Meghan, Li, Helen, Litterman, Nadia, Kolesnikov, Alexey, Noblin, Elizabeth, Chang, Pi-Chuan, Shastri, Anjali, Dorfman, Elizabeth H., Shringarpure, Suyash, Auton, Adam, Carroll, Andrew, McLean, Cory Y.
Publicado 2021

MUSSEL: Enhanced Bayesian Polygenic Risk Prediction Leveraging Information across Multiple Ancestry Groups

por Jin, Jin, Zhan, Jianan, Zhang, Jingning, Zhao, Ruzhang, O’Connell, Jared, Jiang, Yunxuan, Buyske, Steven, Gignoux, Christopher, Haiman, Christopher, Kenny, Eimear E., Kooperberg, Charles, North, Kari, Koelsch, Bertram L., Wojcik, Genevieve, Zhang, Haoyu, Chatterjee, Nilanjan
Publicado 2023

The UK Biobank resource with deep phenotyping and genomic data

por Bycroft, Clare, Freeman, Colin, Petkova, Desislava, Band, Gavin, Elliott, Lloyd T., Sharp, Kevin, Motyer, Allan, Vukcevic, Damjan, Delaneau, Olivier, O’Connell, Jared, Cortes, Adrian, Welsh, Samantha, Young, Alan, Effingham, Mark, McVean, Gil, Leslie, Stephen, Allen, Naomi, Donnelly, Peter, Marchini, Jonathan
Publicado 2018

Multicohort analysis of the maternal age effect on recombination

por Martin, Hilary C., Christ, Ryan, Hussin, Julie G., O'Connell, Jared, Gordon, Scott, Mbarek, Hamdi, Hottenga, Jouke-Jan, McAloney, Kerrie, Willemsen, Gonnecke, Gasparini, Paolo, Pirastu, Nicola, Montgomery, Grant W., Navarro, Pau, Soranzo, Nicole, Toniolo, Daniela, Vitart, Veronique, Wilson, James F., Marchini, Jonathan, Boomsma, Dorret I., Martin, Nicholas G., Donnelly, Peter
Publicado 2015

Influence of autozygosity on common disease risk across the phenotypic spectrum

por Malawsky, Daniel S., van Walree, Eva, Jacobs, Benjamin M., Heng, Teng Hiang, Huang, Qin Qin, Sabir, Ataf H., Rahman, Saadia, Sharif, Saghira Malik, Khan, Ahsan, Mirkov, Maša Umićević, Kuwahara, Hiroyuki, Gao, Xin, Alkuraya, Fowzan S., Posthuma, Danielle, Newman, William G., Griffiths, Christopher J., Mathur, Rohini, van Heel, David A., Finer, Sarah, O’Connell, Jared, Martin, Hilary C.
Publicado 2023

A General Approach for Haplotype Phasing across the Full Spectrum of Relatedness

por O'Connell, Jared, Gurdasani, Deepti, Delaneau, Olivier, Pirastu, Nicola, Ulivi, Sheila, Cocca, Massimiliano, Traglia, Michela, Huang, Jie, Huffman, Jennifer E., Rudan, Igor, McQuillan, Ruth, Fraser, Ross M., Campbell, Harry, Polasek, Ozren, Asiki, Gershim, Ekoru, Kenneth, Hayward, Caroline, Wright, Alan F., Vitart, Veronique, Navarro, Pau, Zagury, Jean-Francois, Wilson, James F., Toniolo, Daniela, Gasparini, Paolo, Soranzo, Nicole, Sandhu, Manjinder S., Marchini, Jonathan
Publicado 2014

Novel insights into the genetics of smoking behaviour, lung function, and chronic obstructive pulmonary disease (UK BiLEVE): a genetic association study in UK Biobank

por Wain, Louise V, Shrine, Nick, Miller, Suzanne, Jackson, Victoria E, Ntalla, Ioanna, Artigas, María Soler, Billington, Charlotte K, Kheirallah, Abdul Kader, Allen, Richard, Cook, James P, Probert, Kelly, Obeidat, Ma'en, Bossé, Yohan, Hao, Ke, Postma, Dirkje S, Paré, Peter D, Ramasamy, Adaikalavan, Mägi, Reedik, Mihailov, Evelin, Reinmaa, Eva, Melén, Erik, O'Connell, Jared, Frangou, Eleni, Delaneau, Olivier, Freeman, Colin, Petkova, Desislava, McCarthy, Mark, Sayers, Ian, Deloukas, Panos, Hubbard, Richard, Pavord, Ian, Hansell, Anna L, Thomson, Neil C, Zeggini, Eleftheria, Morris, Andrew P, Marchini, Jonathan, Strachan, David P, Tobin, Martin D, Hall, Ian P
Publicado 2015

The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease

por Astle, William J., Elding, Heather, Jiang, Tao, Allen, Dave, Ruklisa, Dace, Mann, Alice L., Mead, Daniel, Bouman, Heleen, Riveros-Mckay, Fernando, Kostadima, Myrto A., Lambourne, John J., Sivapalaratnam, Suthesh, Downes, Kate, Kundu, Kousik, Bomba, Lorenzo, Berentsen, Kim, Bradley, John R., Daugherty, Louise C., Delaneau, Olivier, Freson, Kathleen, Garner, Stephen F., Grassi, Luigi, Guerrero, Jose, Haimel, Matthias, Janssen-Megens, Eva M., Kaan, Anita, Kamat, Mihir, Kim, Bowon, Mandoli, Amit, Marchini, Jonathan, Martens, Joost H.A., Meacham, Stuart, Megy, Karyn, O’Connell, Jared, Petersen, Romina, Sharifi, Nilofar, Sheard, Simon M., Staley, James R., Tuna, Salih, van der Ent, Martijn, Walter, Klaudia, Wang, Shuang-Yin, Wheeler, Eleanor, Wilder, Steven P., Iotchkova, Valentina, Moore, Carmel, Sambrook, Jennifer, Stunnenberg, Hendrik G., Di Angelantonio, Emanuele, Kaptoge, Stephen, Kuijpers, Taco W., Carrillo-de-Santa-Pau, Enrique, Juan, David, Rico, Daniel, Valencia, Alfonso, Chen, Lu, Ge, Bing, Vasquez, Louella, Kwan, Tony, Garrido-Martín, Diego, Watt, Stephen, Yang, Ying, Guigo, Roderic, Beck, Stephan, Paul, Dirk S., Pastinen, Tomi, Bujold, David, Bourque, Guillaume, Frontini, Mattia, Danesh, John, Roberts, David J., Ouwehand, Willem H., Butterworth, Adam S., Soranzo, Nicole
Publicado 2016