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Journal of Biomolecular Techniques : JBT
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June 14, 2021
Staff Scientist Perspectives on Onboarding and Professional Development: A Case Study
Melissa M Murphy, H Richard Johnston, Michael E Zwick
Angewandte Chemie (International Ed. in English)
|
May 12, 2021
Direct Immunodetection of Global A-to-I RNA Editing Activity with a Chemiluminescent Bioassay
Steve D Knutson, Robert A Arthur, H Richard Johnston, et al.
Journal of the American Chemical Society
|
February 29, 2020
Selective Enrichment of A-to-I Edited Transcripts from Cellular RNA Using Endonuclease V
Steve D Knutson, Robert A Arthur, H Richard Johnston, et al.
Plos Genetics
|
May 7, 2016
Testing Rare-Variant Association without Calling Genotypes Allows for Systematic Differences in Sequencing between Cases and Controls
Yi-Juan Hu, Peizhou Liao, H Richard Johnston, et al.
Plos Computational Biology
|
August 13, 2015
One Size Doesn't Fit All - RefEditor: Building Personalized Diploid Reference Genome to Improve Read Mapping and Genotype Calling in Next Generation Sequencing Studies
Shuai Yuan, H Richard Johnston, Guosheng Zhang, et al.
BMC Medical Genomics
|
June 10, 2021
Sex-specific recombination patterns predict parent of origin for recurrent genomic disorders
Trenell J Mosley, H Richard Johnston, David J Cutler, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
September 17, 2017
Reply to Plüss et al.: The strength of PEMapper/PECaller lies in unbiased calling using large sample sizes
H Richard Johnston, Pankaj Chopra, Thomas S Wingo, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
February 23, 2017
PEMapper and PECaller provide a simplified approach to whole-genome sequencing
H Richard Johnston, Pankaj Chopra, Thomas S Wingo, et al.
Journal of Psychosomatic Research
|
October 13, 2023
Associations of differentially expressed genes with psychoneurological symptoms in patients with head and neck cancer: A longitudinal study
Yufen Lin, Gang Peng, Deborah W Bruner, et al.
Frontiers in Neurology
|
August 1, 2022
Novel Missense <i>CNTNAP2</i> Variant Identified in Two Consanguineous Pakistani Families With Developmental Delay, Epilepsy, Intellectual Disability, and Aggressive Behavior
Noor Badshah, Kari A Mattison, Sohail Ahmad, et al.
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Search research articles
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Showing results (1-10 of 24) with videos related to
Sort By:
Page
of 3
Journal of Biomolecular Techniques : JBT
|
June 14, 2021
Staff Scientist Perspectives on Onboarding and Professional Development: A Case Study
Melissa M Murphy, H Richard Johnston, Michael E Zwick
Angewandte Chemie (International Ed. in English)
|
May 12, 2021
Direct Immunodetection of Global A-to-I RNA Editing Activity with a Chemiluminescent Bioassay
Steve D Knutson, Robert A Arthur, H Richard Johnston, et al.
Journal of the American Chemical Society
|
February 29, 2020
Selective Enrichment of A-to-I Edited Transcripts from Cellular RNA Using Endonuclease V
Steve D Knutson, Robert A Arthur, H Richard Johnston, et al.
Plos Genetics
|
May 7, 2016
Testing Rare-Variant Association without Calling Genotypes Allows for Systematic Differences in Sequencing between Cases and Controls
Yi-Juan Hu, Peizhou Liao, H Richard Johnston, et al.
Plos Computational Biology
|
August 13, 2015
One Size Doesn't Fit All - RefEditor: Building Personalized Diploid Reference Genome to Improve Read Mapping and Genotype Calling in Next Generation Sequencing Studies
Shuai Yuan, H Richard Johnston, Guosheng Zhang, et al.
BMC Medical Genomics
|
June 10, 2021
Sex-specific recombination patterns predict parent of origin for recurrent genomic disorders
Trenell J Mosley, H Richard Johnston, David J Cutler, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
September 17, 2017
Reply to Plüss et al.: The strength of PEMapper/PECaller lies in unbiased calling using large sample sizes
H Richard Johnston, Pankaj Chopra, Thomas S Wingo, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
February 23, 2017
PEMapper and PECaller provide a simplified approach to whole-genome sequencing
H Richard Johnston, Pankaj Chopra, Thomas S Wingo, et al.
Journal of Psychosomatic Research
|
October 13, 2023
Associations of differentially expressed genes with psychoneurological symptoms in patients with head and neck cancer: A longitudinal study
Yufen Lin, Gang Peng, Deborah W Bruner, et al.
Frontiers in Neurology
|
August 1, 2022
Novel Missense <i>CNTNAP2</i> Variant Identified in Two Consanguineous Pakistani Families With Developmental Delay, Epilepsy, Intellectual Disability, and Aggressive Behavior
Noor Badshah, Kari A Mattison, Sohail Ahmad, et al.
Page
of 3