Vyzkoušejte nový nástroj s podporou AI
Summon Research Assistant
BETA
Reanalysis of Trio Whole-Genome Sequencing Data Doubles the Yield in Autism Spectrum Disorder: De Novo Variants Present in Half
Bar, Omri, Vahey, Elizabeth, Mintz, Mark, Frye, Richard E., Boles, Richard G.
Published in International journal of molecular sciences (01.01.2024)
Published in International journal of molecular sciences (01.01.2024)
Get full text
Journal Article
Copy Number Variation Identification on 3,800 Alzheimer’s Disease Whole Genome Sequencing Data from the Alzheimer’s Disease Sequencing Project
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
Published in Frontiers in genetics (04.11.2021)
Published in Frontiers in genetics (04.11.2021)
Get full text
Journal Article
Rainbow: a tool for large-scale whole-genome sequencing data analysis using cloud computing
Zhao, Shanrong, Prenger, Kurt, Smith, Lance, Messina, Thomas, Fan, Hongtao, Jaeger, Edward, Stephens, Susan
Published in BMC genomics (27.06.2013)
Published in BMC genomics (27.06.2013)
Get full text
Journal Article
Investigation of short tandem repeats in major depression using whole-genome sequencing data
Yu, Chenglong, Baune, Bernhard T., Wong, Ma-Li, Licinio, Julio
Published in Journal of affective disorders (01.05.2018)
Published in Journal of affective disorders (01.05.2018)
Get full text
Journal Article
Whole genome sequencing data of Leptospira weilii and Leptospira kirschneri isolated from human subjects of Sri Lanka
Senavirathna, Indika, Jayasundara, Dinesha, Warnasekara, Janith, Matthias, Michael A., Vinetz, Joseph M., Agampodi, Suneth
Published in Data in brief (01.02.2024)
Published in Data in brief (01.02.2024)
Get full text
Journal Article
A dual-clustering framework for association screening with whole genome sequencing data and longitudinal traits
Liu, Ying, Huang, ChienHsun, Hu, Inchi, Lo, Shaw-Hwa, Zheng, Tian
Published in BMC proceedings (17.06.2014)
Published in BMC proceedings (17.06.2014)
Get full text
Journal Article
Accelerating Medicines Partnership: Parkinson's Disease. Genetic Resource
Iwaki, Hirotaka, Leonard, Hampton L., Makarious, Mary B., Bookman, Matt, Landin, Barry, Vismer, David, Casey, Bradford, Gibbs, J. Raphael, Hernandez, Dena G., Blauwendraat, Cornelis, Vitale, Daniel, Song, Yeajin, Kumar, Dinesh, Dalgard, Clifton L., Sadeghi, Mahdiar, Dong, Xianjun, Misquitta, Leonie, Scholz, Sonja W., Scherzer, Clemens R., Nalls, Mike A., Biswas, Shameek, Singleton, Andrew B.
Published in Movement disorders (01.08.2021)
Published in Movement disorders (01.08.2021)
Get full text
Journal Article
A cost-effective, high-throughput, highly accurate genotyping method for outbred populations
Chen, Denghui, Chitre, Apurva S, Nguyen, Khai-Minh H, Cohen, Katerina A, Peng, Beverly F, Ziegler, Kendra S, Okamoto, Faith, Lin, Bonnie, Johnson, Benjamin B, Sanches, Thiago M, Cheng, Riyan, Polesskaya, Oksana, Palmer, Abraham A
Published in G3 : genes - genomes - genetics (05.02.2025)
Published in G3 : genes - genomes - genetics (05.02.2025)
Get full text
Journal Article
Long‐Read Sequencing Resolves a Complex Structural Variant in PRKN Parkinson's Disease
Daida, Kensuke, Funayama, Manabu, Billingsley, Kimberley J., Malik, Laksh, Miano‐Burkhardt, Abigail, Leonard, Hampton L., Makarious, Mary B., Iwaki, Hirotaka, Ding, Jinhui, Gibbs, J. Raphael, Ishiguro, Mayu, Yoshino, Hiroyo, Ogaki, Kotaro, Oyama, Genko, Nishioka, Kenya, Nonaka, Risa, Akamatsu, Wado, Blauwendraat, Cornelis, Hattori, Nobutaka
Published in Movement disorders (01.12.2023)
Published in Movement disorders (01.12.2023)
Get full text
Journal Article
Large-scale differentiation of iPSC-derived motor neurons from ALS and control subjects
Workman, Michael J., Lim, Ryan G., Wu, Jie, Frank, Aaron, Ornelas, Loren, Panther, Lindsay, Galvez, Erick, Perez, Daniel, Meepe, Imara, Lei, Susan, Valencia, Viviana, Gomez, Emilda, Liu, Chunyan, Moran, Ruby, Pinedo, Louis, Tsitkov, Stanislav, Ho, Ritchie, Kaye, Julia A., Thompson, Terri, Rothstein, Jeffrey D., Finkbeiner, Steven, Fraenkel, Ernest, Sareen, Dhruv, Thompson, Leslie M., Svendsen, Clive N.
Published in Neuron (Cambridge, Mass.) (19.04.2023)
Published in Neuron (Cambridge, Mass.) (19.04.2023)
Get full text
Journal Article
A library of induced pluripotent stem cells from clinically well-characterized, diverse healthy human individuals
Schaniel, Christoph, Dhanan, Priyanka, Hu, Bin, Xiong, Yuguang, Raghunandan, Teeya, Gonzalez, David M., Dariolli, Rafael, D'Souza, Sunita L., Yadaw, Arjun S., Hansen, Jens, Jayaraman, Gomathi, Mathew, Bino, Machado, Moara, Berger, Seth I., Tripodi, Joseph, Najfeld, Vesna, Garg, Jalaj, Miller, Marc, Surlyn, Colleen S., Michelis, Katherine C., Tangirala, Neelima C., Weerahandi, Himali, Thomas, David C., Beaumont, Kristin G., Sebra, Robert, Mahajan, Milind, Schadt, Eric, Vidovic, Dusica, Schürer, Stephan C., Goldfarb, Joseph, Azeloglu, Evren U., Birtwistle, Marc R., Sobie, Eric A., Kovacic, Jason C., Dubois, Nicole C., Iyengar, Ravi
Published in Stem cell reports (14.12.2021)
Published in Stem cell reports (14.12.2021)
Get full text
Journal Article
Genome sequencing of the extinct Eurasian wild aurochs, Bos primigenius, illuminates the phylogeography and evolution of cattle
Park, Stephen D E, Magee, David A., McGettigan, Paul A., Teasdale, Matthew D., Edwards, Ceiridwen J., Lohan, Amanda J., Murphy, Alison, Braud, Martin, Donoghue, Mark T., Liu, Yuan, Chamberlain, Andrew T., Rue-Albrecht, Kévin, Schroeder, Steven, Spillane, Charles, Tai, Shuaishuai, Bradley, Daniel G., Sonstegard, Tad S., Loftus, Brendan J., MacHugh, David E.
Published in Genome Biology (26.10.2015)
Published in Genome Biology (26.10.2015)
Get full text
Journal Article
Low-Frequency Synonymous Coding Variation in CYP2R1 Has Large Effects on Vitamin D Levels and Risk of Multiple Sclerosis
Manousaki, Despoina, Dudding, Tom, Haworth, Simon, Hsu, Yi-Hsiang, Liu, Ching-Ti, Medina-Gómez, Carolina, Voortman, Trudy, van der Velde, Nathalie, Melhus, Håkan, Robinson-Cohen, Cassianne, Cousminer, Diana L., Nethander, Maria, Vandenput, Liesbeth, Noordam, Raymond, Forgetta, Vincenzo, Greenwood, Celia M.T., Biggs, Mary L., Psaty, Bruce M., Rotter, Jerome I., Zemel, Babette S., Mitchell, Jonathan A., Taylor, Bruce, Lorentzon, Mattias, Karlsson, Magnus, Jaddoe, Vincent V.W., Tiemeier, Henning, Campos-Obando, Natalia, Franco, Oscar H., Utterlinden, Andre G., Broer, Linda, van Schoor, Natasja M., Ham, Annelies C., Ikram, M. Arfan, Karasik, David, de Mutsert, Renée, Rosendaal, Frits R., den Heijer, Martin, Wang, Thomas J., Lind, Lars, Orwoll, Eric S., Mook-Kanamori, Dennis O., Michaëlsson, Karl, Kestenbaum, Bryan, Ohlsson, Claes, Mellström, Dan, de Groot, Lisette C.P.G.M., Grant, Struan F.A., Kiel, Douglas P., Zillikens, M. Carola, Rivadeneira, Fernando, Sawcer, Stephen, Timpson, Nicholas J., Richards, J. Brent
Published in American journal of human genetics (03.08.2017)
Published in American journal of human genetics (03.08.2017)
Get full text
Journal Article
Structural variation detection and association analysis of whole‐genome‐sequence data from 16,543 Alzheimer's disease sequencing project subjects
Wang, Hui, Dombroski, Beth A., Cheng, Po‐Liang, Tucci, Albert, Si, Ya‐Qin, Farrell, John J., Tzeng, Jung‐Ying, Leung, Yuk Yee, Malamon, John S., Wang, Li‐San, Vardarajan, Badri N., Farrer, Lindsay A., Schellenberg, Gerard D., Lee, Wan‐Ping
Published in Alzheimer's & dementia (01.06.2025)
Published in Alzheimer's & dementia (01.06.2025)
Get full text
Journal Article