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Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program
Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program
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Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program

Taliun, Daniel ; Kessler, Michael D ; Carlson, Jedidiah ; Taliun, Sarah A Gagliano ; Kang, Hyun Min ; Tian, Xiaowen ; Browning, Brian L ; Clarke, Wayne E ; Loesch, Douglas P ; Shetty, Amol C ; Blackwell, Thomas W ; Smith, Albert V ; Liu, Xiaoming ; Conomos, Matthew P ; Bobo, Dean M ; Aguet, François ; Arking, Dan E ; Aslibekyan, Stella ; Auer, Paul L ; Barnard, John ; Barr, R Graham ; Barwick, Lucas ; Becker, Lewis C ; Bielak, Lawrence F ; Bowden, Donald W ; Brody, Jennifer A ; Burchard, Esteban G ; Cade, Brian E ; Chasman, Daniel I ; Chen, Yii-Der Ida ; Choi, Seung Hoan ; Chung, Mina K ; Correa, Adolfo ; Curran, Joanne E ; Custer, Brian ; Daya, Michelle ; DeMeo, Dawn L ; Ellinor, Patrick T ; Eng, Celeste ; Fingerlin, Tasha ; Forer, Lukas ; Fullerton, Stephanie M ; Germer, Soren ; Gottlieb, Daniel J ; Guo, Xiuqing ; He, Jiang ; Heckbert, Susan R ; Kelly, Tanika ; Kelly, Shannon ; Kenny, Eimear E ; Klemmer, Robert ; Konkle, Barbara A ; Kooperberg, Charles ; Köttgen, Anna ; Lasky-Su, Jessica ; Levy, Daniel ; Lin, Xihong ; Liu, Chunyu ; Lubitz, Steven A ; Mak, Angel C Y ; Manichaikul, Ani ; Manning, Alisa K ; Mathias, Rasika A ; McManus, David D ; Meigs, James B ; Meyers, Deborah A ; Montasser, May E ; Montgomery, Courtney ; Morrison, Alanna C ; Murabito, Joanne M ; Nelson, Sarah C ; North, Kari E ; Peloso, Gina M ; Peyser, Patricia A ; Post, Wendy S ; Rao, D C ; Redline, Susan ; Roden, Dan ; Sarnowski, Chloé ; Schwartz, David A ; Sheehan, Vivien A ; Smith, Nicholas L ; Smith, Jennifer A ; Sotoodehnia, Nona ; Tang, Weihong ; Taylor, Kent D ; Telen, Marilyn ; Tracy, Russell P ; Vasan, Ramachandran S ; Viaud-Martinez, Karine A ; Vrieze, Scott ; Weeks, Daniel E ; Weiss, Scott T ; Gan, Weiniu ; Nickerson, Deborah A ; Browning, Sharon R ; Wilson, James G ; Laurie, Cathy C ; Hernandez, Ryan D ; Abecasis, Gonçalo R

Nature (London), 2021-02, Vol.590 (7845), p.290-299 [Periódico revisado por pares]

England: Nature Publishing Group

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2
Sequencing of human genomes with nanopore technology
Sequencing of human genomes with nanopore technology
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Sequencing of human genomes with nanopore technology

Bowden, Rory ; Davies, Robert W ; Heger, Andreas ; Pagnamenta, Alistair T ; de Cesare, Mariateresa ; Oikkonen, Laura E ; Parkes, Duncan ; Freeman, Colin ; Dhalla, Fatima ; Patel, Smita Y ; Popitsch, Niko ; Ip, Camilla L C ; Roberts, Hannah E ; Salatino, Silvia ; Lockstone, Helen ; Lunter, Gerton ; Taylor, Jenny C ; Buck, David ; Simpson, Michael A ; Donnelly, Peter

Nature communications, 2019-04, Vol.10 (1), p.1869-9, Article 1869 [Periódico revisado por pares]

England: Nature Publishing Group

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3
Opportunities and challenges in long-read sequencing data analysis
Opportunities and challenges in long-read sequencing data analysis
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Opportunities and challenges in long-read sequencing data analysis

Amarasinghe, Shanika L ; Su, Shian ; Dong, Xueyi ; Zappia, Luke ; Ritchie, Matthew E ; Gouil, Quentin

Genome Biology, 2020-02, Vol.21 (1), p.30-30, Article 30 [Periódico revisado por pares]

England: BioMed Central Ltd

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4
SMOOTH-seq: single-cell genome sequencing of human cells on a third-generation sequencing platform
SMOOTH-seq: single-cell genome sequencing of human cells on a third-generation sequencing platform
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SMOOTH-seq: single-cell genome sequencing of human cells on a third-generation sequencing platform

Fan, Xiaoying ; Yang, Cheng ; Li, Wen ; Bai, Xiuzhen ; Zhou, Xin ; Xie, Haoling ; Wen, Lu ; Tang, Fuchou

Genome Biology, 2021-06, Vol.22 (1), p.195-195, Article 195 [Periódico revisado por pares]

England: BioMed Central Ltd

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5
Whole genome sequencing reveals that genetic conditions are frequent in intensively ill children
Whole genome sequencing reveals that genetic conditions are frequent in intensively ill children
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Whole genome sequencing reveals that genetic conditions are frequent in intensively ill children

French, Courtney E. ; Delon, Isabelle ; Dolling, Helen ; Sanchis-Juan, Alba ; Shamardina, Olga ; Mégy, Karyn ; Abbs, Stephen ; Austin, Topun ; Bowdin, Sarah ; Branco, Ricardo G. ; Firth, Helen ; Rowitch, David H. ; Raymond, F. Lucy

Intensive care medicine, 2019-05, Vol.45 (5), p.627-636 [Periódico revisado por pares]

Berlin/Heidelberg: Springer Berlin Heidelberg

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6
Global mapping of cancers: The Cancer Genome Atlas and beyond
Global mapping of cancers: The Cancer Genome Atlas and beyond
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Global mapping of cancers: The Cancer Genome Atlas and beyond

Ganini, Carlo ; Amelio, Ivano ; Bertolo, Riccardo ; Bove, Pierluigi ; Buonomo, Oreste Claudio ; Candi, Eleonora ; Cipriani, Chiara ; Di Daniele, Nicola ; Juhl, Hartmut ; Mauriello, Alessandro ; Marani, Carla ; Marshall, John ; Melino, Sonia ; Marchetti, Paolo ; Montanaro, Manuela ; Natale, Maria Emanuela ; Novelli, Flavia ; Palmieri, Giampiero ; Piacentini, Mauro ; Rendina, Erino Angelo ; Roselli, Mario ; Sica, Giuseppe ; Tesauro, Manfredi ; Rovella, Valentina ; Tisone, Giuseppe ; Shi, Yufang ; Wang, Ying ; Melino, Gerry

Molecular oncology, 2021-11, Vol.15 (11), p.2823-2840 [Periódico revisado por pares]

United States: John Wiley & Sons, Inc

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7
Rapid, Sensitive, Full-Genome Sequencing of Severe Acute Respiratory Syndrome Coronavirus 2
Rapid, Sensitive, Full-Genome Sequencing of Severe Acute Respiratory Syndrome Coronavirus 2
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Rapid, Sensitive, Full-Genome Sequencing of Severe Acute Respiratory Syndrome Coronavirus 2

Paden, Clinton R ; Tao, Ying ; Queen, Krista ; Zhang, Jing ; Li, Yan ; Uehara, Anna ; Tong, Suxiang

Emerging infectious diseases, 2020-10, Vol.26 (10), p.2401-2405 [Periódico revisado por pares]

United States: U.S. National Center for Infectious Diseases

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8
Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole-genome sequencing studies at scale
Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole-genome sequencing studies at scale
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Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole-genome sequencing studies at scale

Li, Xihao ; Li, Zilin ; Zhou, Hufeng ; Gaynor, Sheila M ; Liu, Yaowu ; Chen, Han ; Sun, Ryan ; Dey, Rounak ; Arnett, Donna K ; Aslibekyan, Stella ; Ballantyne, Christie M ; Bielak, Lawrence F ; Blangero, John ; Boerwinkle, Eric ; Bowden, Donald W ; Broome, Jai G ; Conomos, Matthew P ; Correa, Adolfo ; Cupples, L Adrienne ; Curran, Joanne E ; Freedman, Barry I ; Guo, Xiuqing ; Hindy, George ; Irvin, Marguerite R ; Kardia, Sharon L R ; Kathiresan, Sekar ; Khan, Alyna T ; Kooperberg, Charles L ; Laurie, Cathy C ; Liu, X Shirley ; Mahaney, Michael C ; Manichaikul, Ani W ; Martin, Lisa W ; Mathias, Rasika A ; McGarvey, Stephen T ; Mitchell, Braxton D ; Montasser, May E ; Moore, Jill E ; Morrison, Alanna C ; O'Connell, Jeffrey R ; Palmer, Nicholette D ; Pampana, Akhil ; Peralta, Juan M ; Peyser, Patricia A ; Psaty, Bruce M ; Redline, Susan ; Rice, Kenneth M ; Rich, Stephen S ; Smith, Jennifer A ; Tiwari, Hemant K ; Tsai, Michael Y ; Vasan, Ramachandran S ; Wang, Fei Fei ; Weeks, Daniel E ; Weng, Zhiping ; Wilson, James G ; Yanek, Lisa R ; Neale, Benjamin M ; Sunyaev, Shamil R ; Abecasis, Gonçalo R ; Rotter, Jerome I ; Willer, Cristen J ; Peloso, Gina M ; Natarajan, Pradeep ; Lin, Xihong

Nature genetics, 2020-09, Vol.52 (9), p.969-983 [Periódico revisado por pares]

United States: Nature Publishing Group

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9
Stakeholder views on secondary findings in whole-genome and whole-exome sequencing: a systematic review of quantitative and qualitative studies
Stakeholder views on secondary findings in whole-genome and whole-exome sequencing: a systematic review of quantitative and qualitative studies
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Stakeholder views on secondary findings in whole-genome and whole-exome sequencing: a systematic review of quantitative and qualitative studies

Mackley, Michael P. ; Fletcher, Benjamin ; Parker, Michael ; Watkins, Hugh ; Ormondroyd, Elizabeth

Genetics in medicine, 2017-03, Vol.19 (3), p.283-293 [Periódico revisado por pares]

United States: Elsevier Inc

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10
Real-Time Whole-Genome Sequencing for Surveillance of Listeria monocytogenes, France
Real-Time Whole-Genome Sequencing for Surveillance of Listeria monocytogenes, France
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Real-Time Whole-Genome Sequencing for Surveillance of Listeria monocytogenes, France

Moura, Alexandra ; Tourdjman, Mathieu ; Leclercq, Alexandre ; Hamelin, Estelle ; Laurent, Edith ; Fredriksen, Nathalie ; Van Cauteren, Dieter ; Bracq-Dieye, Hélène ; Thouvenot, Pierre ; Vales, Guillaume ; Tessaud-Rita, Nathalie ; Maury, Mylène M ; Alexandru, Andreea ; Criscuolo, Alexis ; Quevillon, Emmanuel ; Donguy, Marie-Pierre ; Enouf, Vincent ; de Valk, Henriette ; Brisse, Sylvain ; Lecuit, Marc

Emerging infectious diseases, 2017-09, Vol.23 (9), p.1462-1470 [Periódico revisado por pares]

United States: U.S. National Center for Infectious Diseases

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