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Brent S. Pedersen

Utah System of Higher Education

50H-index
166Paper Count
1.4WCitation Count
Published Papers 52
Publication Date
The Utah NeoSeq Project: a collaborative multidisciplinary program to facilitate genomic diagnostics in the neonatal intensive care unit
err2025-03-23
err0
errOAAI
errJenkins, Sabrina Malone; Palmquist, Rachel N.; Moore, Barry; Boyden, Steven E.; Nicholas, Thomas J.; Bayrak-Toydemir, Pinar; Mao, Rong; Farrell, J. Andrew R.; Holt, Carson H.; Rynearson, Shawn G.; Solorzano, Chelsea M.; Ward, Alistair; Best, D. Hunter; Al-Sweel, Najla; Bentley, Dawn L.; Brunelli, Luca; Chow, Clement Y.; Close, Devin W.; Cormier, Michael J.; Deshotel, Malia J.; Durtschi, Jacob; Eide, Erik J.; Floyd, Luaiva; Fredrickson, Eric K.; Fulmer, Makenzie L.; Hernandez, Edgar J.; Kapron, Ashley L.; Karren, Mary Anne; Lewis, Robert G.; Miller, Christine E.; Murtaugh, L. Charles; Nicholson, Kelsey E.; Noble, Katherine; O'Fallon, Brendan D.; O'Shea, John M.; Pattison, David C.; Pedersen, Brent S.; Petersen, Brandy J.; Peterson, Bennet D.; Pizzo, Lucilla; Reynolds, Hayley M.; Rindler, Paul; Torr, Carrie B.; Wen, Ting; Yost, H. Joseph; Zhao, Jian; Yandell, Mark; Marth, Gabor T.; Quinlan, Aaron R.; Carey, John C.; Shayota, Brian J.; Tristani-Firouzi, Martin; Bonkowsky, Joshua L.
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Identification of CNTN2 as a genetic modifier of PIGA-CDG in a family with incomplete penetrance and in Drosophila
err2025-02-01
err0
PREAI
errThorpe, Holly J.; Pedersen, Brent S.; Dietze, Miranda; Link, Nichole; Quinlan, Aaron R.; Bonkowsky, Joshua L.; Thomas, Ashley; Chow, Clement Y.
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Vcfexpress: flexible, rapid user-expressions to filter and format VCFs
err2024-03-03
err0
errOAAI
errPedersen, Brent S.; Quinlan, Aaron R.
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STRling: a k-mer counting approach that detects short tandem repeat expansions at known and novel loci
err2022-12-14
err23
errOAAI
errDashnow, Harriet; Pedersen, Brent S.; Hiatt, Laurel; Brown, Joe; Beecroft, Sarah J.; Ravenscroft, Gianina; LaCroix, Amy J.; Lamont, Phillipa; Roxburgh, Richard H.; Rodrigues, Miriam J.; Davis, Mark; Mefford, Heather C.; Laing, Nigel G.; Quinlan, Aaron R.
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Extensive Recombination-driven Coronavirus Diversification Expands the Pool of Potential Pandemic Pathogens
err2022-11-04
err15
errOAAI
errGoldstein, Stephen A.; Brown, Joe; Pedersen, Brent S.; Quinlan, Aaron R.; Elde, Nels C.
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Searching thousands of genomes to classify somatic and novel structural variants using STIX (vol 19, pg 445, 2022)
err2022-05-26
err0
errOAAI
errChowdhury, Murad; Pedersen, Brent S.; Sedlazeck, Fritz J.; Quinlan, Aaron R.; Layer, Ryan M.
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Searching thousands of genomes to classify somatic and novel structural variants using STIX
err2022-04-08
err6
errOAAI
errChowdhury, Murad; Pedersen, Brent S.; Sedlazeck, Fritz J.; Quinlan, Aaron R.; Layer, Ryan M.
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Samplot: a platform for structural variant visual validation and automated filtering
err2021-05-25
err53
errOAAI
errBelyeu, Jonathan R.; Chowdhury, Murad; Brown, Joseph; Pedersen, Brent S.; Cormier, Michael J.; Quinlan, Aaron R.; Layer, Ryan M.
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Go Get Data (GGD) is a framework that facilitates reproducible access to genomic data
err2021-04-12
err8
errOAAI
errCormier, Michael J.; Belyeu, Jonathan R.; Pedersen, Brent S.; Brown, Joseph; Koester, Johannes; Quinlan, Aaron R.
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De novo structural mutation rates and gamete-of-origin biases revealed through genome sequencing of 2,396 families
err2021-04-01
err56
errOAAI
errBelyeu, Jonathan R.; Brand, Harrison; Wang, Harold; Zhao, Xuefang; Pedersen, Brent S.; Feusier, Julie; Gupta, Meenal; Nicholas, Thomas J.; Brown, Joseph; Baird, Lisa; Devlin, Bernie; Sanders, Stephan J.; Jorde, Lynn B.; Talkowski, Michael E.; Quinlan, Aaron R.
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SUICIDE DEATHS SELECTED FOR GENETIC RISK: POLYGENIC RISK SCORE CHARACTERISTICS AND HIGH-IMPACT SEQUENCE VARIANTS
err2019-10-01
err0
PREAI
errCoon, Hilary; Shabalin, Andrey; DiBlasi, Emily; Keeshin, Brooks; Bakian, Amanda; Ferris, Elliott; Callor, William B.; Velinder, Matt; Pedersen, Brent; Christensen, Erik; Quinlan, Aaron; Marth, Gabor; Li, Qingqin; Gray, Douglas; Docherty, Anna
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Large, three-generation human families reveal post-zygotic mosaicism and variability in germline mutation accumulation
err2019-09-24
err114
errOAAI
errSasani, Thomas A.; Pedersen, Brent S.; Gao, Ziyue; Baird, Lisa; Przeworski, Molly; Jorde, Lynn B.; Quinlan, Aaron R.
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Overlooked roles of DNA damage and maternal age in generating human germline mutations
err2019-04-24
err130
errOAAI
errGao, Ziyue; Moorjani, Priya; Sasani, Thomas A.; Pedersen, Brent S.; Quinlan, Aaron R.; Jorde, Lynn B.; Amster, Guy; Przeworski, Molly
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A map of constrained coding regions in the human genome
err2018-12-10
err162
errOAAI
errHavrilla, James M.; Pedersen, Brent S.; Layer, Ryan M.; Quinlan, Aaron R.
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GOATOOLS: A Python library for Gene Ontology analyses
err2018-07-18
err748
errOAAI
errKlopfenstein, D. V.; Zhang, Liangsheng; Pedersen, Brent S.; Ramirez, Fidel; Vesztrocy, Alex Warwick; Naldi, Aurelien; Mungall, Christopher J.; Yunes, Jeffrey M.; Botvinnik, Olga; Weigel, Mark; Dampier, Will; Dessimoz, Christophe; Flick, Patrick; Tang, Haibao
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SV-plaudit: A cloud-based framework for manually curating thousands of structural variants
err2018-05-31
err27
errOAAI
errBelyeu, Jonathan R.; Nicholas, Thomas J.; Pedersen, Brent S.; Sasani, Thomas A.; Havrilla, James M.; Kravitz, Stephanie N.; Conway, Megan E.; Lohman, Brian K.; Quinlan, Aaron R.; Layer, Ryan M.
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