日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

SAIGE-GPU: accelerating genome- and phenome-wide association studies using GPUs

SAIGE-GPU:利用GPU加速全基因组和全表型关联研究

Rodriguez, Alex; Kim, Youngdae; Nandi, Tarak Nath; Keat, Karl; Kumar, Rachit; Conery, Mitchell; Bhukar, Rohan; Liu, Molei; Hessington, John; Maheshwari, Ketan; Begoli, Edmon; Tourassi, Georgia; Muralidhar, Sumitra; Natarajan, Pradeep; Voight, Benjamin F; Cho, Kelly; Gaziano, John Michael; Damrauer, Scott M; Liao, Katherine P; Zhou, Wei; Huffman, Jennifer E; Verma, Anurag; Madduri, Ravi K

Common-variant and rare-variant genetic architecture of heart failure across the allele-frequency spectrum

心力衰竭的常见变异和罕见变异遗传结构在等位基因频率谱中的分布

Lee, David S M; Cardone, Kathleen M; Zhang, David Y; Tsao, Noah L; Abramowitz, Sarah; Sharma, Pranav; DePaolo, John S; Conery, Mitchell; Aragam, Krishna G; Biddinger, Kiran; Dikilitas, Ozan; Hoffman-Andrews, Lily; Judy, Renae L; Khan, Atlas; Kullo, Iftikhar J; Puckelwartz, Megan J; Reza, Nosheen; Satterfield, Benjamin A; Singhal, Pankhuri; Arany, Zoltan; Cappola, Thomas P; Carruth, Eric D; Day, Sharlene M; Do, Ron; Haggerty, Christopher M; Joseph, Jacob; McNally, Elizabeth M; Nadkarni, Girish; Owens, Anjali T; Rader, Daniel J; Ritchie, Marylyn D; Sun, Yan V; Voight, Benjamin F; Levin, Michael G; Damrauer, Scott M

GWAS-informed data integration and non-coding CRISPRi screen illuminate genetic etiology of bone mineral density.

GWAS 信息数据整合和非编码 CRISPRi 筛选揭示骨矿物质密度的遗传病因。

Conery Mitchell, Pippin James A, Wagley Yadav, Trang Khanh, Pahl Matthew C, Villani David A, Favazzo Lacey J, Ackert-Bicknell Cheryl L, Zuscik Michael J, Katsevich Eugene, Wells Andrew D, Zemel Babette S, Voight Benjamin F, Hankenson Kurt D, Chesi Alessandra, Grant Struan F A

Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program

多样性和规模:退伍军人事务部百万退伍军人计划中2068个性状的遗传结构

Verma, Anurag; Huffman, Jennifer E; Rodriguez, Alex; Conery, Mitchell; Liu, Molei; Ho, Yuk-Lam; Kim, Youngdae; Heise, David A; Guare, Lindsay; Panickan, Vidul Ayakulangara; Garcon, Helene; Linares, Franciel; Costa, Lauren; Goethert, Ian; Tipton, Ryan; Honerlaw, Jacqueline; Davies, Laura; Whitbourne, Stacey; Cohen, Jeremy; Posner, Daniel C; Sangar, Rahul; Murray, Michael; Wang, Xuan; Dochtermann, Daniel R; Devineni, Poornima; Shi, Yunling; Nandi, Tarak Nath; Assimes, Themistocles L; Brunette, Charles A; Carroll, Robert J; Clifford, Royce; Duvall, Scott; Gelernter, Joel; Hung, Adriana; Iyengar, Sudha K; Joseph, Jacob; Kember, Rachel; Kranzler, Henry; Kripke, Colleen M; Levey, Daniel; Luoh, Shiuh-Wen; Merritt, Victoria C; Overstreet, Cassie; Deak, Joseph D; Grant, Struan F A; Polimanti, Renato; Roussos, Panos; Shakt, Gabrielle; Sun, Yan V; Tsao, Noah; Venkatesh, Sanan; Voloudakis, Georgios; Justice, Amy; Begoli, Edmon; Ramoni, Rachel; Tourassi, Georgia; Pyarajan, Saiju; Tsao, Philip; O'Donnell, Christopher J; Muralidhar, Sumitra; Moser, Jennifer; Casas, Juan P; Bick, Alexander G; Zhou, Wei; Cai, Tianxi; Voight, Benjamin F; Cho, Kelly; Gaziano, J Michael; Madduri, Ravi K; Damrauer, Scott; Liao, Katherine P

Common- and rare-variant genetic architecture of heart failure across the allele frequency spectrum

心力衰竭常见和罕见变异的遗传结构在等位基因频率谱中的分布

Lee, David S M; Cardone, Kathleen M; Zhang, David Y; Tsao, Noah L; Abramowitz, Sarah; Sharma, Pranav; DePaolo, John S; Conery, Mitchell; Aragam, Krishna G; Biddinger, Kiran; Dilitikas, Ozan; Hoffman-Andrews, Lily; Judy, Renae L; Khan, Atlas; Kulo, Iftikhar; Puckelwartz, Megan J; Reza, Nosheen; Satterfield, Benjamin A; Singhal, Pankhuri; Arany, Zoltan P; Cappola, Thomas P; Carruth, Eric; Day, Sharlene M; Do, Ron; Haggarty, Christopher M; Joseph, Jacob; McNally, Elizabeth M; Nadkarni, Girish; Owens, Anjali T; Rader, Daniel J; Ritchie, Marylyn D; Sun, Yan V; Voight, Benjamin F; Levin, Michael G; Damrauer, Scott M

Accelerating Genome- and Phenome-Wide Association Studies using GPUs - A case study using data from the Million Veteran Program

利用GPU加速全基因组和全表型关联研究——以百万退伍军人计划的数据为例

Rodriguez, Alex; Kim, Youngdae; Nandi, Tarak Nath; Keat, Karl; Kumar, Rachit; Bhukar, Rohan; Conery, Mitchell; Liu, Molei; Hessington, John; Maheshwari, Ketan; Schmidt, Drew; Begoli, Edmon; Tourassi, Georgia; Muralidhar, Sumitra; Natarajan, Pradeep; Voight, Benjamin F; Cho, Kelly; Gaziano, J Michael; Damrauer, Scott M; Liao, Katherine P; Zhou, Wei; Huffman, Jennifer E; Verma, Anurag; Madduri, Ravi K

Regularized sequence-context mutational trees capture variation in mutation rates across the human genome

规则化的序列上下文突变树能够捕捉人类基因组中突变率的变化

Adams, Christopher J; Conery, Mitchell; Auerbach, Benjamin J; Jensen, Shane T; Mathieson, Iain; Voight, Benjamin F

Human height: a model common complex trait

人类身高:一种常见的复杂性状

Conery, Mitchell; Grant, Struan F A

Diversity and Scale: Genetic Architecture of 2,068 Traits in the VA Million Veteran Program.

多样性和规模:退伍军人事务部百万退伍军人计划中 2,068 个性状的遗传结构

Verma Anurag, Huffman Jennifer E, Rodriguez Alex, Conery Mitchell, Liu Molei, Ho Yuk-Lam, Kim Youngdae, Heise David A, Guare Lindsay, Panickan Vidul Ayakulangara, Garcon Helene, Linares Franciel, Costa Lauren, Goethert Ian, Tipton Ryan, Honerlaw Jacqueline, Davies Laura, Whitbourne Stacey, Cohen Jeremy, Posner Daniel C, Sangar Rahul, Murray Michael, Wang Xuan, Dochtermann Daniel R, Devineni Poornima, Shi Yunling, Nandi Tarak Nath, Assimes Themistocles L, Brunette Charles A, Carroll Robert J, Clifford Royce, Duvall Scott, Gelernter Joel, Hung Adriana, Iyengar Sudha K, Joseph Jacob, Kember Rachel, Kranzler Henry, Levey Daniel, Luoh Shiuh-Wen, Merritt Victoria C, Overstreet Cassie, Deak Joseph D, Grant Struan F A, Polimanti Renato, Roussos Panos, Sun Yan V, Venkatesh Sanan, Voloudakis Georgios, Justice Amy, Begoli Edmon, Ramoni Rachel, Tourassi Georgia, Pyarajan Saiju, Tsao Philip S, O'Donnell Christopher J, Muralidhar Sumitra, Moser Jennifer, Casas Juan P, Bick Alexander G, Zhou Wei, Cai Tianxi, Voight Benjamin F, Cho Kelly, Gaziano Michael J, Madduri Ravi K, Damrauer Scott M, Liao Katherine P

Copy Number Variation Identification on 3,800 Alzheimer's Disease Whole Genome Sequencing Data from the Alzheimer's Disease Sequencing Project

对来自阿尔茨海默病测序项目的3800例阿尔茨海默病全基因组测序数据进行拷贝数变异鉴定

Lee, Wan-Ping; Tucci, Albert A; Conery, Mitchell; Leung, Yuk Yee; Kuzma, Amanda B; Valladares, Otto; Chou, Yi-Fan; Lu, Wenbin; Wang, Li-San; Schellenberg, Gerard D; Tzeng, Jung-Ying