Search Results - Aaron R Quinlan

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  1. 1

    Epistasis between mutator alleles contributes to germline mutation spectrum variability in laboratory mice by Thomas A Sasani, Aaron R Quinlan, Kelley Harris

    Published in eLife (2024-02-01)
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  2. 2

    Long read sequencing reveals poxvirus evolution through rapid homogenization of gene arrays by Thomas A Sasani, Kelsey R Cone, Aaron R Quinlan, Nels C Elde

    Published in eLife (2018-08-01)
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  3. 3

    XPRESSyourself: Enhancing, standardizing, and automating ribosome profiling computational analyses yields improved insight into data. by Jordan A Berg, Jonathan R Belyeu, Jeffrey T Morgan, Yeyun Ouyang, Alex J Bott, Aaron R Quinlan, Jason Gertz, Jared Rutter

    Published in PLoS Computational Biology (2020-01-01)
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  4. 4

    CaBagE: A Cas9-based Background Elimination strategy for targeted, long-read DNA sequencing. by Amelia D Wallace, Thomas A Sasani, Jordan Swanier, Brooke L Gates, Jeff Greenland, Brent S Pedersen, Katherine E Varley, Aaron R Quinlan

    Published in PLoS ONE (2021-01-01)
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  5. 5

    STRchive: a dynamic resource detailing population-level and locus-specific insights at tandem repeat disease loci by Laurel Hiatt, Ben Weisburd, Egor Dolzhenko, Vincent Rubinetti, Akshay K. Avvaru, Grace E. VanNoy, Nehir Edibe Kurtas, Heidi L. Rehm, Aaron R. Quinlan, Harriet Dashnow

    Published in Genome Medicine (2025-03-01)
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  6. 6

    Whole-genome sequencing analysis in families with recurrent pregnancy loss: A pilot study. by Tsegaselassie Workalemahu, Cecile Avery, Sarah Lopez, Nathan R Blue, Amelia Wallace, Aaron R Quinlan, Hilary Coon, Derek Warner, Michael W Varner, D Ware Branch, Lynn B Jorde, Robert M Silver

    Published in PLoS ONE (2023-01-01)
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  7. 7

    The Utah NeoSeq Project: a collaborative multidisciplinary program to facilitate genomic diagnostics in the neonatal intensive care unit by Sabrina Malone Jenkins, Rachel N. Palmquist, Barry Moore, Steven E. Boyden, Thomas J. Nicholas, Pinar Bayrak-Toydemir, Rong Mao, J. Andrew R. Farrell, Carson H. Holt, Shawn G. Rynearson, Chelsea M. Solorzano, Alistair Ward, D. Hunter Best, Najla Al-Sweel, Dawn L. Bentley, Luca Brunelli, Clement Y. Chow, Devin W. Close, Michael J. Cormier, Malia J. Deshotel, Jacob Durtschi, Erik J. Eide, Luaiva Floyd, Eric K. Fredrickson, Makenzie L. Fulmer, Edgar J. Hernandez, Ashley L. Kapron, Mary Anne Karren, Robert G. Lewis, Christine E. Miller, L. Charles Murtaugh, Kelsey E. Nicholson, Katherine Noble, Brendan D. O’Fallon, John M. O’Shea, David C. Pattison, Brent S. Pedersen, Brandy J. Petersen, Bennet D. Peterson, Lucilla Pizzo, Hayley M. Reynolds, Paul Rindler, Carrie B. Torr, Ting Wen, H. Joseph Yost, Jian Zhao, Mark Yandell, Gabor T. Marth, Aaron R. Quinlan, John C. Carey, Brian J. Shayota, Martin Tristani-Firouzi, Joshua L. Bonkowsky

    Published in npj Genomic Medicine (2025-03-01)
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