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American Journal of Human Genetics
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February 13, 2025
Identification of CNTN2 as a genetic modifier of PIGA-CDG in a family with incomplete penetrance and in Drosophila
Holly J Thorpe, Brent S Pedersen, Miranda Dietze, et al.
International Journal of Radiation Oncology, Biology, Physics
|
October 15, 2017
Identification of ATIC as a Novel Target for Chemoradiosensitization
Xiangfei Liu, Uma Devi Paila, Sharon N Teraoka, et al.
Plos Computational Biology
|
February 1, 2020
XPRESSyourself: Enhancing, standardizing, and automating ribosome profiling computational analyses yields improved insight into data
Jordan A Berg, Jonathan R Belyeu, Jeffrey T Morgan, et al.
Biorxiv : the Preprint Server for Biology
|
August 30, 2024
Identification of <i>CNTN2</i> as a genetic modifier of PIGA-CDG through pedigree analysis of a family with incomplete penetrance and functional testing in <i>Drosophila</i>
Holly J Thorpe, Brent S Pedersen, Miranda Dietze, et al.
Plos One
|
April 8, 2021
CaBagE: A Cas9-based Background Elimination strategy for targeted, long-read DNA sequencing
Amelia D Wallace, Thomas A Sasani, Jordan Swanier, et al.
Genome Research
|
February 16, 2013
Breakpoint profiling of 64 cancer genomes reveals numerous complex rearrangements spawned by homology-independent mechanisms
Ankit Malhotra, Michael Lindberg, Gregory G Faust, et al.
Genome Research
|
March 24, 2010
Genome-wide mapping and assembly of structural variant breakpoints in the mouse genome
Aaron R Quinlan, Royden A Clark, Svetlana Sokolova, et al.
Genome Research
|
May 16, 2012
Copy number variation detection and genotyping from exome sequence data
Niklas Krumm, Peter H Sudmant, Arthur Ko, et al.
Diabetes
|
December 4, 2015
Targeted Deep Sequencing in Multiple-Affected Sibships of European Ancestry Identifies Rare Deleterious Variants in PTPN22 That Confer Risk for Type 1 Diabetes
Yan Ge, Suna Onengut-Gumuscu, Aaron R Quinlan, et al.
Genome Medicine
|
March 27, 2025
STRchive: a dynamic resource detailing population-level and locus-specific insights at tandem repeat disease loci
Laurel Hiatt, Ben Weisburd, Egor Dolzhenko, et al.
Page
of 11
Search research articles
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Showing results (61-70 of 104) with videos related to
Sort By:
Page
of 11
American Journal of Human Genetics
|
February 13, 2025
Identification of CNTN2 as a genetic modifier of PIGA-CDG in a family with incomplete penetrance and in Drosophila
Holly J Thorpe, Brent S Pedersen, Miranda Dietze, et al.
International Journal of Radiation Oncology, Biology, Physics
|
October 15, 2017
Identification of ATIC as a Novel Target for Chemoradiosensitization
Xiangfei Liu, Uma Devi Paila, Sharon N Teraoka, et al.
Plos Computational Biology
|
February 1, 2020
XPRESSyourself: Enhancing, standardizing, and automating ribosome profiling computational analyses yields improved insight into data
Jordan A Berg, Jonathan R Belyeu, Jeffrey T Morgan, et al.
Biorxiv : the Preprint Server for Biology
|
August 30, 2024
Identification of <i>CNTN2</i> as a genetic modifier of PIGA-CDG through pedigree analysis of a family with incomplete penetrance and functional testing in <i>Drosophila</i>
Holly J Thorpe, Brent S Pedersen, Miranda Dietze, et al.
Plos One
|
April 8, 2021
CaBagE: A Cas9-based Background Elimination strategy for targeted, long-read DNA sequencing
Amelia D Wallace, Thomas A Sasani, Jordan Swanier, et al.
Genome Research
|
February 16, 2013
Breakpoint profiling of 64 cancer genomes reveals numerous complex rearrangements spawned by homology-independent mechanisms
Ankit Malhotra, Michael Lindberg, Gregory G Faust, et al.
Genome Research
|
March 24, 2010
Genome-wide mapping and assembly of structural variant breakpoints in the mouse genome
Aaron R Quinlan, Royden A Clark, Svetlana Sokolova, et al.
Genome Research
|
May 16, 2012
Copy number variation detection and genotyping from exome sequence data
Niklas Krumm, Peter H Sudmant, Arthur Ko, et al.
Diabetes
|
December 4, 2015
Targeted Deep Sequencing in Multiple-Affected Sibships of European Ancestry Identifies Rare Deleterious Variants in PTPN22 That Confer Risk for Type 1 Diabetes
Yan Ge, Suna Onengut-Gumuscu, Aaron R Quinlan, et al.
Genome Medicine
|
March 27, 2025
STRchive: a dynamic resource detailing population-level and locus-specific insights at tandem repeat disease loci
Laurel Hiatt, Ben Weisburd, Egor Dolzhenko, et al.
Page
of 11