Hasil Pencarian - Michael Eberle

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  1. 1
    P146: Complete resolution of genes with highly homologous gene family members or pseudogenes using long-read PacBio HiFi sequencing*

    P146: Complete resolution of genes with highly homologous gene family members or pseudogenes using long-read PacBio HiFi sequencing* oleh Xiao Chen, Michael Eberle

    Diterbitkan 2023-01-01
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  2. 2
    P600: pb-StarPhase: A phase-aware pharmacogenomic diplotyper for long-read sequencing data

    P600: pb-StarPhase: A phase-aware pharmacogenomic diplotyper for long-read sequencing data oleh James Holt, John Harting, Nina Gonzaludo, Zev Kronenberg, Christopher Saunders, Michael Eberle

    Diterbitkan 2024-01-01
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  3. 3
    P819: Genome-wide resolution of highly homologous genes using long-read PacBio HiFi sequencing*

    P819: Genome-wide resolution of highly homologous genes using long-read PacBio HiFi sequencing* oleh Xiao Chen, Egor Dolzhenko, Emily Farrow, Isabelle Thiffault, Alexander Hoischen, Tomi Pastinen, Michael Eberle

    Diterbitkan 2024-01-01
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  4. 4
    Enabling End-Users in Designing and Executing of Complex, Collaborative Robotic Processes

    Enabling End-Users in Designing and Executing of Complex, Collaborative Robotic Processes oleh Helmut Zörrer, Georg Weichhart, Mathias Schmoigl Tonis, Till Bieg, Matthias Propst, Dominik Schuster, Nadine Sturm, Chloé Nativel, Gabriele Salomon, Felix Strohmeier, Andreas Sackl, Michael Eberle, Andreas Pichler

    Diterbitkan 2023-05-01
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  5. 5
    O36: Long-read genome sequencing in unsolved rare genetic diseases: Preliminary experiences from the Care4Rare Canada Consortium

    O36: Long-read genome sequencing in unsolved rare genetic diseases: Preliminary experiences from the Care4Rare Canada Consortium oleh Giulia Del Gobbo, Madeline Couse, Christine Lambert, Siyuan Zhang, Harsharan Dhillon, Cairbre Fanslow, William Rowell, Egor Dolzhenko, Guilherme De Sena Brandine, Michael Eberle, Christian Marshall, Kristin Kernohan, Kym Boycott

    Diterbitkan 2024-01-01
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  6. 6
    P293: Long read sequencing analysis of 120 samples with known and challenging-to-detect clinical variants

    P293: Long read sequencing analysis of 120 samples with known and challenging-to-detect clinical variants oleh Joseph Devaney, Jessica Noya, April Berlyoung, Aaron Johnson, Julianna Spangler, Rhonda Brandon, Kathleen Hruska, Lucas Lochovsky, Egor Dolzhenko, Xiao Chen, Michael Eberle, Alexander Robertson, Paul Kruszka, Gustavo Stolovitzky, Scott Newman

    Diterbitkan 2024-01-01
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