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Genome-wide genetic marker discovery and genotyping using next-generation sequencing
Genome-wide genetic marker discovery and genotyping using next-generation sequencing
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Genome-wide genetic marker discovery and genotyping using next-generation sequencing

Davey, John W ; Hohenlohe, Paul A ; Etter, Paul D ; Boone, Jason Q ; Catchen, Julian M ; Blaxter, Mark L

Nature reviews. Genetics, 2011-07, Vol.12 (7), p.499-510 [Periódico revisado por pares]

London: Nature Publishing Group

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2
Predictive functional profiling of microbial communities using 16S rRNA marker gene sequences
Predictive functional profiling of microbial communities using 16S rRNA marker gene sequences
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Predictive functional profiling of microbial communities using 16S rRNA marker gene sequences

Langille, Morgan G I ; Zaneveld, Jesse ; Caporaso, J Gregory ; McDonald, Daniel ; Knights, Dan ; Reyes, Joshua A ; Clemente, Jose C ; Burkepile, Deron E ; Vega Thurber, Rebecca L ; Knight, Rob ; Beiko, Robert G ; Huttenhower, Curtis

Nature biotechnology, 2013-09, Vol.31 (9), p.814-821 [Periódico revisado por pares]

United States: Nature Publishing Group

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3
Rare cell variability and drug-induced reprogramming as a mode of cancer drug resistance
Rare cell variability and drug-induced reprogramming as a mode of cancer drug resistance
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Rare cell variability and drug-induced reprogramming as a mode of cancer drug resistance

Shaffer, Sydney M ; Dunagin, Margaret C ; Torborg, Stefan R ; Torre, Eduardo A ; Emert, Benjamin ; Krepler, Clemens ; Beqiri, Marilda ; Sproesser, Katrin ; Brafford, Patricia A ; Xiao, Min ; Eggan, Elliott ; Anastopoulos, Ioannis N ; Vargas-Garcia, Cesar A ; Singh, Abhyudai ; Nathanson, Katherine L ; Herlyn, Meenhard ; Raj, Arjun

Nature (London), 2017-06, Vol.546 (7658), p.431-435 [Periódico revisado por pares]

England: Nature Publishing Group

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4
Determining the Polymorphism Information Content of a molecular marker
Determining the Polymorphism Information Content of a molecular marker
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Determining the Polymorphism Information Content of a molecular marker

Serrote, Caetano Miguel Lemos ; Reiniger, Lia Rejane Silveira ; Silva, Karol Buuron ; Rabaiolli, Silvia Machado dos Santos ; Stefanel, Charlene Moro

Gene, 2020-02, Vol.726, p.144175-144175, Article 144175 [Periódico revisado por pares]

Netherlands: Elsevier B.V

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5
Metagenomic microbial community profiling using unique clade-specific marker genes
Metagenomic microbial community profiling using unique clade-specific marker genes
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Metagenomic microbial community profiling using unique clade-specific marker genes

Segata, Nicola ; Waldron, Levi ; Ballarini, Annalisa ; Narasimhan, Vagheesh ; Jousson, Olivier ; Huttenhower, Curtis

Nature methods, 2012-08, Vol.9 (8), p.811-814 [Periódico revisado por pares]

United States: Nature Publishing Group

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6
Genomic complexity of multiple myeloma and its clinical implications
Genomic complexity of multiple myeloma and its clinical implications
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Genomic complexity of multiple myeloma and its clinical implications

Manier, Salomon ; Salem, Karma Z ; Park, Jihye ; Landau, Dan A ; Getz, Gad ; Ghobrial, Irene M

Nature reviews. Clinical oncology, 2017-02, Vol.14 (2), p.100-113 [Periódico revisado por pares]

England: Nature Publishing Group

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7
Characterization of Greater Middle Eastern genetic variation for enhanced disease gene discovery
Characterization of Greater Middle Eastern genetic variation for enhanced disease gene discovery
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Characterization of Greater Middle Eastern genetic variation for enhanced disease gene discovery

Scott, Eric M ; Halees, Anason ; Itan, Yuval ; Spencer, Emily G ; He, Yupeng ; Azab, Mostafa Abdellateef ; Gabriel, Stacey B ; Belkadi, Aziz ; Boisson, Bertrand ; Abel, Laurent ; Clark, Andrew G ; Alkuraya, Fowzan S ; Casanova, Jean-Laurent ; Gleeson, Joseph G

Nature genetics, 2016-09, Vol.48 (9), p.1071-1076 [Periódico revisado por pares]

United States: Nature Publishing Group

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8
Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects
Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects
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Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects

Marshall, Christian R ; Wu, Wenting ; Antaki, Danny ; Pinto, Dalila ; Wang, Zhouzhi ; Maile, Michelle S ; Agartz, Ingrid ; Albus, Margot ; Amin, Farooq ; Atkins, Joshua ; Bacanu, Silviu A ; Bergen, Sarah E ; Cairns, Murray J ; Cantor, Rita M ; Carrera, Noa ; Catts, Stanley V ; Chambert, Kimberley D ; Cheng, Wei ; Cormican, Paul ; Craddock, Nick ; Crespo-Facorro, Benedicto ; Crowley, James J ; Davidson, Michael ; DeLisi, Lynn E ; Dikeos, Dimitris ; Donohoe, Gary ; Drapeau, Elodie ; Dudbridge, Frank ; Escott-Price, Valentina ; Freimer, Nelson B ; Friedman, Joseph I ; Georgieva, Lyudmila ; Gershon, Elliot S ; Goldstein, Jacqueline I ; Gratten, Jacob ; de Haan, Lieuwe ; Hansen, Mark ; Huang, Hailiang ; Ikeda, Masashi ; Joa, Inge ; Kalaydjieva, Luba ; Kavanagh, David ; Konte, Bettina ; Lee, S Hong ; Lerer, Bernard ; Magnusson, Patrik K E ; Maher, Brion S ; Mattheisen, Manuel ; McIntosh, Andrew M ; Meier, Sandra ; Milanova, Vihra ; Morris, Derek W ; Müller-Myhsok, Bertram ; Nenadic, Igor ; Nestadt, Gerald ; Nordin, Annelie ; O'Dushlaine, Colm ; Olincy, Ann ; Olsen, Line ; Pantelis, Christos ; Papadimitriou, George N ; Parkhomenko, Elena ; Pocklington, Andrew J ; Purcell, Shaun M ; Reichenberg, Abraham ; Reimers, Mark A ; Ruderfer, Douglas M ; Schulze, Thomas G ; Schwab, Sibylle G ; Scolnick, Edward M ; Scott, Rodney J ; Silverman, Jeremy M ; Söderman, Erik ; Strohmaier, Jana ; Suvisaari, Jaana ; Visscher, Peter M ; Webb, Bradley T ; Williams, Nigel M ; Williams, Stephanie ; Wormley, Brandon K ; Zai, Clement C ; Andreassen, Ole A ; Bramon, Elvira ; Daly, Mark J ; Darvasi, Ariel ; Esko, Tõnu ; Gill, Michael ; Jablensky, Assen V ; Jönsson, Erik G ; Kendler, Kenneth S ; McCarroll, Steven A ; Moran, Jennifer L ; Nöthen, Markus M ; Owen, Michael J ; Pato, Carlos N ; St Clair, David ; Walters, James T R ; O'Donovan, Michael C ; Scherer, Stephen W ; Neale, Benjamin M

Nature genetics, 2017-01, Vol.49 (1), p.27-35 [Periódico revisado por pares]

United States: Nature Publishing Group

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9
A Fast Method that Uses Polygenic Scores to Estimate the Variance Explained by Genome-wide Marker Panels and the Proportion of Variants Affecting a Trait
A Fast Method that Uses Polygenic Scores to Estimate the Variance Explained by Genome-wide Marker Panels and the Proportion of Variants Affecting a Trait
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A Fast Method that Uses Polygenic Scores to Estimate the Variance Explained by Genome-wide Marker Panels and the Proportion of Variants Affecting a Trait

Palla, Luigi ; Dudbridge, Frank

American journal of human genetics, 2015-08, Vol.97 (2), p.250-259 [Periódico revisado por pares]

United States: Elsevier Inc

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10
M-CAP eliminates a majority of variants of uncertain significance in clinical exomes at high sensitivity
M-CAP eliminates a majority of variants of uncertain significance in clinical exomes at high sensitivity
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M-CAP eliminates a majority of variants of uncertain significance in clinical exomes at high sensitivity

Jagadeesh, Karthik A ; Wenger, Aaron M ; Berger, Mark J ; Guturu, Harendra ; Stenson, Peter D ; Cooper, David N ; Bernstein, Jonathan A ; Bejerano, Gill

Nature genetics, 2016-12, Vol.48 (12), p.1581-1586 [Periódico revisado por pares]

United States: Nature Publishing Group

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