检索结果 - Ryan M. Layer
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Whole-genome analysis for effective clinical diagnosis and gene discovery in early infantile epileptic encephalopathy 由 Betsy Ostrander, Russell J. Butterfield, Brent S. Pedersen, Andrew Farrell, Ryan M. Layer, Alistair Ward, Chase Miller, Tonya DiSera, Francis Filloux, Meghan Candee, Tara Newcomb, Joshua L. Bonkowsky, Gábor Marth, Aaron R. Quinlan
出版 2018Artigo -
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Mapping and characterization of structural variation in 17,795 human genomes 由 Haley Abel, David E. Larson, Allison Regier, Colby Chiang, Indraniel Das, Krishna Kanchi, Ryan M. Layer, Benjamin M. Neale, William Salerno, Catherine Reeves, Steven Buyske, Tara C. Matise, Donna M. Muzny, Michael C. Zody, Eric S. Lander, Susan K. Dutcher, Nathan O. Stitziel, Ira M. Hall
出版 2020Artigo -
17
The structural variation landscape in 492 Atlantic salmon genomes 由 Alicia C. Bertolotti, Ryan M. Layer, Manu Kumar Gundappa, Michael D. Gallagher, Ege Pehlivanoglu, Torfinn Nome, Diego Robledo, Matthew Kent, Line L. Røsæg, Matilde Mengkrog Holen, Teshome Mulugeta, Thomas J. Ashton, Kjetil Hindar, Harald Sægrov, Bjørn Florø‐Larsen, Jaakko Erkinaro, Craig R. Primmer, Louis Bernatchez, Samuel Martín, Ian A. Johnston, Simen R. Sandve, Sigbjørn Lien, Daniel J. Macqueen
出版 2020Artigo -
18
Combating subclonal evolution of resistant cancer phenotypes 由 Samuel W. Brady, Jasmine A. McQuerry, 義行 高橋, Stephen Piccolo, Gajendra Shrestha, David F. Jenkins, Ryan M. Layer, Brent S. Pedersen, R.H. Miller, Amanda Esch, Sara R. Selitsky, Joel S. Parker, Layla A. Anderson, Brian K. Dalley, Rachel E. Factor, Chakravarthy B. Reddy, Jonathan Boltax, Dean Y. Li, Philip J. Moos, Joe W. Gray, Laura M. Heiser, Saundra S. Buys, Adam L. Cohen, W. Evan Johnson, Aaron R. Quinlan, Gábor Marth, Theresa L. Werner, Andrea H. Bild
出版 2017Artigo -
19
A complete reference genome improves analysis of human genetic variation 由 Sergey Aganezov, Stephanie M. Yan, Daniela C. Soto, Melanie Kirsche, Samantha Zarate, Pavel Avdeyev, Dylan J. Taylor, Kishwar Shafin, Alaina Shumate, Chunlin Xiao, Justin Wagner, Jennifer McDaniel, Nathan D. Olson, Michael Sauria, Mitchell R. Vollger, Arang Rhie, Melissa Meredith, Skylar Martin, Joyce Lee, Sergey Koren, Jeffrey Rosenfeld, Benedict Paten, Ryan M. Layer, Chen-Shan Chin, Fritz J. Sedlazeck, Nancy F. Hansen, Danny E. Miller, Adam M. Phillippy, Karen H. Miga, Rajiv C. McCoy, Megan Y. Dennis, Justin M. Zook, Michael C. Schatz
出版 2021Pré-impressão -
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A complete reference genome improves analysis of human genetic variation 由 Sergey Aganezov, Stephanie M. Yan, Daniela C. Soto, Melanie Kirsche, Samantha Zarate, Pavel Avdeyev, Dylan J. Taylor, Kishwar Shafin, Alaina Shumate, Chunlin Xiao, Justin Wagner, Jennifer McDaniel, Nathan D. Olson, Michael Sauria, Mitchell R. Vollger, Arang Rhie, Melissa Meredith, Skylar Martin, Joyce Lee, Sergey Koren, Jeffrey Rosenfeld, Benedict Paten, Ryan M. Layer, Chen-Shan Chin, Fritz J. Sedlazeck, Nancy F. Hansen, Danny E. Miller, Adam M. Phillippy, Karen H. Miga, Rajiv C. McCoy, Megan Y. Dennis, Justin M. Zook, Michael C. Schatz
出版 2022Artigo
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Biology
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Structural variation
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Human genome
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Cell biology
Evolutionary biology
False positive paradox
Gene expression
Human genetics
MyoD
Myocyte
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Phenotype
Population
Reference genome
Transcription factor
Annotation
Breakpoint
Cancer research
Cellular differentiation
Chromosomal translocation
Coding region
Copy-number variation