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Andrew S Allen

Showing results (81-90 of 101) with videos related to

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Cell Genomics|February 6, 2025
Characterization and bioinformatic filtering of ambient gRNAs in single-cell CRISPR screens using CLEANSERSiyan Liu, Marisa C Hamilton, Thomas Cowart, et al.
BMC Infectious Diseases|February 15, 2014
A genome-wide association study of variants associated with acquisition of Staphylococcus aureus bacteremia in a healthcare settingCharlotte L Nelson, Kimberly Pelak, Mihai V Podgoreanu, et al.
Bioinformatics (Oxford, England)|June 1, 2011
SVA: software for annotating and visualizing sequenced human genomesDongliang Ge, Elizabeth K Ruzzo, Kevin V Shianna, et al.
Plos Genetics|May 9, 2018
De novo and inherited private variants in MAP1B in periventricular nodular heterotopiaErin L Heinzen, Adam C O'Neill, Xiaolin Zhu, et al.
Plos Genetics|November 30, 2017
A case-control collapsing analysis identifies epilepsy genes implicated in trio sequencing studies focused on de novo mutationsXiaolin Zhu, Raghavendra Padmanabhan, Brett Copeland, et al.
Nature Genetics|November 9, 2023
Transcriptional and epigenetic regulators of human CD8<sup>+</sup> T cell function identified through orthogonal CRISPR screensSean R McCutcheon, Adam M Swartz, Michael C Brown, et al.
Plos Computational Biology|October 2, 2018
meaRtools: An R package for the analysis of neuronal networks recorded on microelectrode arraysSahar Gelfman, Quanli Wang, Yi-Fan Lu, et al.
Biorxiv : the Preprint Server for Biology|June 4, 2025
Cell Modeling and Rescue of a Novel Non-coding Genetic Cause of Glycogen Storage Disease IXApoorva K Iyengar, Xue Zou, Jian Dai, et al.
Journal of the American Society of Nephrology : JASN|May 16, 2019
Exome-Based Rare-Variant Analyses in CKDSophia Cameron-Christie, Charles J Wolock, Emily Groopman, et al.
Genetics in Medicine Open|February 20, 2026
Cell modeling and rescue of a novel noncoding genetic cause of glycogen storage disease IXApoorva K Iyengar, Xue Zou, Jian Dai, et al.
Pageof 11

Showing results (81-90 of 101) with videos related to

Sort By:
Pageof 11
Cell Genomics|February 6, 2025
Characterization and bioinformatic filtering of ambient gRNAs in single-cell CRISPR screens using CLEANSERSiyan Liu, Marisa C Hamilton, Thomas Cowart, et al.
BMC Infectious Diseases|February 15, 2014
A genome-wide association study of variants associated with acquisition of Staphylococcus aureus bacteremia in a healthcare settingCharlotte L Nelson, Kimberly Pelak, Mihai V Podgoreanu, et al.
Bioinformatics (Oxford, England)|June 1, 2011
SVA: software for annotating and visualizing sequenced human genomesDongliang Ge, Elizabeth K Ruzzo, Kevin V Shianna, et al.
Plos Genetics|May 9, 2018
De novo and inherited private variants in MAP1B in periventricular nodular heterotopiaErin L Heinzen, Adam C O'Neill, Xiaolin Zhu, et al.
Plos Genetics|November 30, 2017
A case-control collapsing analysis identifies epilepsy genes implicated in trio sequencing studies focused on de novo mutationsXiaolin Zhu, Raghavendra Padmanabhan, Brett Copeland, et al.
Nature Genetics|November 9, 2023
Transcriptional and epigenetic regulators of human CD8<sup>+</sup> T cell function identified through orthogonal CRISPR screensSean R McCutcheon, Adam M Swartz, Michael C Brown, et al.
Plos Computational Biology|October 2, 2018
meaRtools: An R package for the analysis of neuronal networks recorded on microelectrode arraysSahar Gelfman, Quanli Wang, Yi-Fan Lu, et al.
Biorxiv : the Preprint Server for Biology|June 4, 2025
Cell Modeling and Rescue of a Novel Non-coding Genetic Cause of Glycogen Storage Disease IXApoorva K Iyengar, Xue Zou, Jian Dai, et al.
Journal of the American Society of Nephrology : JASN|May 16, 2019
Exome-Based Rare-Variant Analyses in CKDSophia Cameron-Christie, Charles J Wolock, Emily Groopman, et al.
Genetics in Medicine Open|February 20, 2026
Cell modeling and rescue of a novel noncoding genetic cause of glycogen storage disease IXApoorva K Iyengar, Xue Zou, Jian Dai, et al.
Pageof 11