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The following results are related to COVID-19. Are you interested to view more results? Visit OpenAIRE - Explore.
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1,396 research outcomes, page 1 of 140
  • publication . Preprint . Article . 2022
    Open Access English
    Authors:
    Hyungrok Do; Shinjini Nandi; Preston Putzel; Padhraic Smyth; Judy Zhong;
    Persistent Identifiers
    Publisher: Cornell University
    Project: NIH | CVD Risk and Outcome Hete... (5R01AG054467-02), NIH | Clinical and Translationa... (3UL1TR001445-03S1)

    In data collection for predictive modeling, under-representation of certain groups, based on gender, race/ethnicity, or age, may yield less-accurate predictions for these groups. Recently, this issue of fairness in predictions has attracted significant attention, as dat...

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  • publication . Preprint . Article . 2022
    Open Access English
    Authors:
    Rui Wang; Jiahui Chen; Yuta Hozumi; Changchuan Yin; Guo-Wei Wei;
    Persistent Identifiers
    Publisher: Cornell University
    Project: NIH | Synergistic integration o... (1R01GM126189-01A1), NSF | Kinetics-Driven Drug Disc... (1761320)

    The recent global surge in COVID-19 infections has been fueled by new SARS-CoV-2 variants, namely Alpha, Beta, Gamma, Delta, etc. The molecular mechanism underlying such surge is elusive due to 4,653 non-degenerate mutations on the spike protein, which is the target of ...

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  • publication . Preprint . Article . 2022
    Open Access English
    Authors:
    Khanna, Ajay; Larson, David E.; Srivatsan, Sridhar Nonavinkere; Mosior, Matthew; Abbott, Travis E.; Kiwala, Susanna; Ley, Timothy J.; Duncavage, Eric J.; Walter, Matthew J.; Walker, Jason R.; ...
    Persistent Identifiers
    Project: NIH | DEFINING THE REGULATORY, ... (1K22CA188163-01), NIH | Integrated Analysis & Int... (4R00HG007940-03), NIH | COMPREHENSIVE INFORMATIC ... (5R50CA211782-02), NIH | DEVELOPMENT OF INFORMATIC... (5U01CA209936-03), NIH | Genomics of Acute Myeloge... (5P01CA101937-03)

    Bam-readcount is a utility for generating low-level information about sequencing data at specific nucleotide positions. Originally designed to help filter genomic mutation calls, the metrics it outputs are useful as input for variant detection tools and for resolving am...

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