نتائج البحث - Ryan M. Layer
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Vcfanno: fast, flexible annotation of genetic variants حسب Brent S. Pedersen, Ryan M. Layer, Aaron R. Quinlan
منشور في 2016Artigo -
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Regulation of several androgen-induced genes through the repression of the miR-99a/let-7c/miR-125b-2 miRNA cluster in prostate cancer cells حسب Dongxiao Sun, Ryan M. Layer, Adam C. Mueller, Magdalena A. Cichewicz, Masahiko Negishi, Bryce M. Paschal, Anindya Dutta
منشور في 2013Artigo -
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Breakpoint profiling of 64 cancer genomes reveals numerous complex rearrangements spawned by homology-independent mechanisms حسب Ankit Malhotra, Michael Lindberg, Gregory G. Faust, Mitchell L. Leibowitz, Royden A. Clark, Ryan M. Layer, Aaron R. Quinlan, Ira M. Hall
منشور في 2013Artigo -
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SV-plaudit: A cloud-based framework for manually curating thousands of structural variants حسب Jonathan R. Belyeu, T. Nicholas, Brent S. Pedersen, Thomas A. Sasani, James M. Havrilla, Stephanie N. Kravitz, Megan E. Conway, Brian K. Lohman, Aaron R. Quinlan, Ryan M. Layer
منشور في 2018Artigo -
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Whole-genome analysis for effective clinical diagnosis and gene discovery in early infantile epileptic encephalopathy حسب 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
منشور في 2018Artigo -
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Mapping and characterization of structural variation in 17,795 human genomes حسب 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
منشور في 2020Artigo -
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The structural variation landscape in 492 Atlantic salmon genomes حسب 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
منشور في 2020Artigo -
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Combating subclonal evolution of resistant cancer phenotypes حسب 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
منشور في 2017Artigo -
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A complete reference genome improves analysis of human genetic variation حسب 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
منشور في 2021Pré-impressão -
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A complete reference genome improves analysis of human genetic variation حسب 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
منشور في 2022Artigo
أدوات البحث:
موضوعات ذات صلة
Biology
Gene
Genetics
Genome
Computational biology
Structural variation
Computer science
Human genome
Artificial intelligence
Medicine
Cancer
Cell biology
Evolutionary biology
False positive paradox
Gene expression
Human genetics
MyoD
Myocyte
Myogenesis
Phenotype
Population
Reference genome
Transcription factor
Annotation
Breakpoint
Cancer research
Cellular differentiation
Chromosomal translocation
Coding region
Copy-number variation