نتائج البحث - Erwin Frise

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  1. 1
    Systematic image‐driven analysis of the spatial <i>Drosophila</i> embryonic expression landscape

    Systematic image‐driven analysis of the spatial <i>Drosophila</i> embryonic expression landscape حسب Erwin Frise, Ann S. Hammonds, S Celniker

    منشور في 2010
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    Artigo
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  2. 2
    Stability-driven nonnegative matrix factorization to interpret spatial gene expression and build local gene networks

    Stability-driven nonnegative matrix factorization to interpret spatial gene expression and build local gene networks حسب Siqi Wu, Antony Joseph, Ann S. Hammonds, S Celniker, Bin Yu, Erwin Frise

    منشور في 2016
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    Artigo
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  3. 3
    The Drosophila Numb protein inhibits signaling of the Notch receptor during cell-cell interaction in sensory organ lineage.

    The Drosophila Numb protein inhibits signaling of the Notch receptor during cell-cell interaction in sensory organ lineage. حسب Erwin Frise, Juergen A. Knoblich, Susan Younger-Shepherd, Lily Yeh Jan, Yuh Nung Jan

    منشور في 1996
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    Artigo
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  4. 4
    Spatial expression of transcription factors in Drosophila embryonic organ development

    Spatial expression of transcription factors in Drosophila embryonic organ development حسب Ann S. Hammonds, Christopher A. Bristow, William W. Fisher, Richard Weiszmann, Siqi Wu, Volker Hartenstein, Manolis Kellis, Bin Yu, Erwin Frise, S Celniker

    منشور في 2013
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    Artigo
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  5. 5
    Automated prioritization of sick newborns for whole genome sequencing using clinical natural language processing and machine learning

    Automated prioritization of sick newborns for whole genome sequencing using clinical natural language processing and machine learning حسب Bennet Peterson, Edgar J. Hernández, Charlotte A. Hobbs, Sabrina Malone Jenkins, Barry Moore, Edwin F. Juarez, Samuel Zoucha, Erica Sanford Kobayashi, Matthew N. Bainbridge, Erwin Frise, Albert Oriol, Luca Brunelli, Stephen F. Kingsmore, Mark Yandell

    منشور في 2023
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    Artigo
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  6. 6
    Fiji: an open-source platform for biological-image analysis

    Fiji: an open-source platform for biological-image analysis حسب Johannes Schindelin, Ignacio Arganda‐Carreras, Erwin Frise, Verena Kaynig, Mark Longair, Tobias Pietzsch, Stephan Preibisch, Curtis Rueden, Stephan Saalfeld, Benjamin Schmid, Jean-Yves Tinévez, Daniel J. White, Volker Hartenstein, Kevin W. Eliceiri, Pavel Tomančák, Albert Cardona

    منشور في 2012
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  7. 7
    Artificial intelligence enables comprehensive genome interpretation and nomination of candidate diagnoses for rare genetic diseases

    Artificial intelligence enables comprehensive genome interpretation and nomination of candidate diagnoses for rare genetic diseases حسب Francisco M. De La Vega, Shimul Chowdhury, Barry Moore, Erwin Frise, Jeanette McCarthy, Edgar J. Hernández, Terence C. Wong, Kiely N. James, Lucia Guidugli, Pankaj B. Agrawal, Casie A. Genetti, Catherine A. Brownstein, Alan H. Beggs, Britt-Sabina Löscher, André Franke, Braden Boone, Shawn Levy, Katrin Õunap, Sander Pajusalu, Matt Huentelman, Keri Ramsey, Marcus Naymik, Vinodh Narayanan, Narayanan Veeraraghavan, Paul R. Billings, Martin G. Reese, Mark Yandell, Stephen F. Kingsmore

    منشور في 2021
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    Artigo
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  8. 8
    Genome sequencing is critical for forecasting outcomes following congenital cardiac surgery

    Genome sequencing is critical for forecasting outcomes following congenital cardiac surgery حسب W. Scott Watkins, Edgar J. Hernández, Thomas A. Miller, Nathan R. Blue, Raquel M. Zimmerman, Eric R. Griffiths, Erwin Frise, Daniel Bernstein, Marko T. Boskovski, Martina Brueckner, Wendy K. Chung, J. William Gaynor, Bruce D. Gelb, Elizabeth Goldmuntz, Peter J. Gruber, Jane W. Newburger, Amy E. Roberts, Sarah U. Morton, John E. Mayer, Christine E. Seidman, Jonathan G. Seidman, Yufeng Shen, Michael Wagner, H. Joseph Yost, Mark Yandell, Martin Tristani‐Firouzi

    منشور في 2025
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    Artigo
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  9. 9
    Finishing a whole-genome shotgun: Release 3 of the Drosophila melanogastereuchromatic genome sequence

    Finishing a whole-genome shotgun: Release 3 of the Drosophila melanogastereuchromatic genome sequence حسب S Celniker, David A. Wheeler, Brent A. Kronmiller, Joseph W. Carlson, Aaron L. Halpern, Sandeep Patel, Mark D. Adams, Mark Champe, Shannon Dugan, Erwin Frise, Ann Hodgson, Reed George, Roger A. Hoskins, Todd Laverty, Donna M. Muzny, Catherine R. Nelson, Joanne Pacleb, Soo Hyung Park, Barret D. Pfeiffer, Stephen M. Richards, Erica Sodergren, Robert Svirskas, Paul E. Tabor, Kenneth H. Wan, Mark Stapleton, Granger G. Sutton, Craig Venter, George M. Weinstock, Steven E. Scherer, Eugene W. Myers, Richard A. Gibbs, Gerald M. Rubin

    منشور في 2002
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    Artigo
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  10. 10
    Diversity and dynamics of the Drosophila transcriptome

    Diversity and dynamics of the Drosophila transcriptome حسب James Brown, Nathan Boley, Robert C. Eisman, Gemma E. May, Marcus H. Stoiber, Michael O. Duff, Ben W. Booth, Jiayu Wen, Soo Hyung Park, Ana Maria Suzuki, Kenneth H. Wan, Charles Yu, Dayu Zhang, Joseph W. Carlson, Lucy Cherbas, Brian D. Eads, David F. Miller, Keithanne Mockaitis, Johnny Roberts, Carrie Davis, Erwin Frise, Ann S. Hammonds, Sara Olson, Sol Shenker, David Sturgill, Anastasia Samsonova, Richard Weiszmann, Garret Robinson, Juan Hernandez, Justen Andrews, Peter J. Bickel, Piero Carninci, Peter Cherbas, T Gingeras, Roger A. Hoskins, Thomas C. Kaufman, Eric C. Lai, Brian Oliver, Norbert Perrimon, Brenton R. Graveley, S Celniker

    منشور في 2014
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    Artigo
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  11. 11
    A genome sequencing system for universal newborn screening, diagnosis, and precision medicine for severe genetic diseases

    A genome sequencing system for universal newborn screening, diagnosis, and precision medicine for severe genetic diseases حسب Stephen F. Kingsmore, Laurie D. Smith, Chris M. Kunard, Matthew Bainbridge, Serge Batalov, Wendy Benson, Eric Blincow, Sara Caylor, Christina Chambers, Guillermo del Angel, David Dimmock, Yan Ding, Katarzyna A. Ellsworth, Annette Feigenbaum, Erwin Frise, Robert C. Green, Lucia Guidugli, Kevin P. Hall, Christian Holm Hansen, Charlotte A. Hobbs, Scott D. Kahn, Mark J. Kiel, Lucita Van Der Kraan, Chad Krilow, Yong Hyun Kwon, Lakshminarasimha Madhavrao, Jennie Le, Sébastien Lefebvre, Rebecca Mardach, William R. Mowrey, Danny Oh, Mallory Owen, George S. Powley, Gunter Scharer, Seth Shelnutt, Mari Tokita, Shyamal Mehtalia, Albert Oriol, Stavros Papadopoulos, James C. Perry, Edwin F. Juarez, Erica Sanford Kobayashi, Steven J. Schwartz, Duke Tran, Martin G. Reese, Meredith S. Wright, Narayanan Veeraraghavan, Kristen Wigby, Mary Willis, Aaron R. Wolen, Thomas Defay

    منشور في 2022
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    Revisão
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  12. 12
    An automated 13.5 hour system for scalable diagnosis and acute management guidance for genetic diseases

    An automated 13.5 hour system for scalable diagnosis and acute management guidance for genetic diseases حسب Mallory Owen, Sébastien Lefebvre, Christian Holm Hansen, Chris M. Kunard, David Dimmock, Laurie D. Smith, Gunter Scharer, Rebecca Mardach, Mary Willis, Annette Feigenbaum, Anna‐Kaisa Niemi, Yan Ding, Luca Van Der Kraan, Katarzyna A. Ellsworth, Lucia Guidugli, Bryan R. Lajoie, Timothy K. McPhail, Shyamal Mehtalia, Kevin Chau, Yong Hyun Kwon, Zhanyang Zhu, Serge Batalov, Shimul Chowdhury, Seema Rego, James C. Perry, Mark Speziale, Mark Nespeca, Meredith S. Wright, Martin G. Reese, Francisco M. De La Vega, Joe Azure, Erwin Frise, Charlene Son Rigby, Sandy White, Charlotte A. Hobbs, Sheldon Gilmer, G. R. Knight, Albert Oriol, Jerica Lenberg, Shareef Nahas, Kate Perofsky, Kyu Kim, Jeanne Carroll, Nicole G. Coufal, Erica Sanford Kobayashi, Kristen Wigby, Jacqueline C. Weir, Vicki S. Thomson, Louise Fraser, Seka Lazare, Yoon H. Shin, Haiying Grunenwald, Richard Lee, David Jones, Duke Tran, Andrew M. Gross, Patrick Daigle, Anne Case, Marisa Lue, James A. Richardson, John Reynders, Thomas Defay, Kevin P. Hall, Narayanan Veeraraghavan, Stephen F. Kingsmore

    منشور في 2022
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    Artigo
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