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Christopher M Watson

Showing results (21-30 of 94) with videos related to

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Human Mutation|October 31, 2019
Long-read nanopore sequencing resolves a TMEM231 gene conversion event causing Meckel-Gruber syndromeChristopher M Watson, Philip Dean, Nick Camm, et al.
Bioinformatics (Oxford, England)|April 12, 2015
GeneTIER: prioritization of candidate disease genes using tissue-specific gene expression profilesAgne Antanaviciute, Catherine Daly, Laura A Crinnion, et al.
Biomed Research International|September 10, 2015
Towards a Next-Generation Sequencing Diagnostic Service for Tumour Genotyping: A Comparison of Panels and PlatformsGeorge J Burghel, Carolyn D Hurst, Christopher M Watson, et al.
Molecular Vision|May 25, 2026
Targeted sequencing with single-molecule molecular inversion probes highlights a gap in understanding the cause of Fuchs endothelial corneal dystrophyBushra Alayed, Danah Albuainain, Salina Siddiqui, et al.
Journal of Clinical Immunology|April 17, 2019
RNAseq Supports the Molecular Genetic Diagnosis of Late-Onset ADA DeficiencyChristopher M Watson, Claire Stockdale, Ian Berry, et al.
Joint Commission Journal on Quality and Patient Safety|December 3, 2011
Simulated pediatric resuscitation use for personal protective equipment adherence measurement and training during the 2009 influenza (H1N1) pandemicChristopher M Watson, Jordan M Duval-Arnould, Michael C McCrory, et al.
Plos One|June 9, 2016
A Chromosome 7 Pericentric Inversion Defined at Single-Nucleotide Resolution Using Diagnostic Whole Genome Sequencing in a Patient with Hand-Foot-Genital SyndromeChristopher M Watson, Laura A Crinnion, Sally M Harrison, et al.
Bioinformatics (Oxford, England)|August 15, 2015
OVA: integrating molecular and physical phenotype data from multiple biomedical domain ontologies with variant filtering for enhanced variant prioritizationAgne Antanaviciute, Christopher M Watson, Sally M Harrison, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|July 6, 2019
Cas9-based enrichment and single-molecule sequencing for precise characterization of genomic duplicationsChristopher M Watson, Laura A Crinnion, Sarah Hewitt, et al.
Surgical Innovation|May 24, 2015
Reducing Accidental Dislodgement of the Percutaneous Endoscopic Gastrostomy: A Prospective Trial of the "SafetyBreak" DeviceLaura H Rosenberger, Christopher A Guidry, John P Davis, et al.
Pageof 10

Showing results (21-30 of 94) with videos related to

Sort By:
Pageof 10
Human Mutation|October 31, 2019
Long-read nanopore sequencing resolves a TMEM231 gene conversion event causing Meckel-Gruber syndromeChristopher M Watson, Philip Dean, Nick Camm, et al.
Bioinformatics (Oxford, England)|April 12, 2015
GeneTIER: prioritization of candidate disease genes using tissue-specific gene expression profilesAgne Antanaviciute, Catherine Daly, Laura A Crinnion, et al.
Biomed Research International|September 10, 2015
Towards a Next-Generation Sequencing Diagnostic Service for Tumour Genotyping: A Comparison of Panels and PlatformsGeorge J Burghel, Carolyn D Hurst, Christopher M Watson, et al.
Molecular Vision|May 25, 2026
Targeted sequencing with single-molecule molecular inversion probes highlights a gap in understanding the cause of Fuchs endothelial corneal dystrophyBushra Alayed, Danah Albuainain, Salina Siddiqui, et al.
Journal of Clinical Immunology|April 17, 2019
RNAseq Supports the Molecular Genetic Diagnosis of Late-Onset ADA DeficiencyChristopher M Watson, Claire Stockdale, Ian Berry, et al.
Joint Commission Journal on Quality and Patient Safety|December 3, 2011
Simulated pediatric resuscitation use for personal protective equipment adherence measurement and training during the 2009 influenza (H1N1) pandemicChristopher M Watson, Jordan M Duval-Arnould, Michael C McCrory, et al.
Plos One|June 9, 2016
A Chromosome 7 Pericentric Inversion Defined at Single-Nucleotide Resolution Using Diagnostic Whole Genome Sequencing in a Patient with Hand-Foot-Genital SyndromeChristopher M Watson, Laura A Crinnion, Sally M Harrison, et al.
Bioinformatics (Oxford, England)|August 15, 2015
OVA: integrating molecular and physical phenotype data from multiple biomedical domain ontologies with variant filtering for enhanced variant prioritizationAgne Antanaviciute, Christopher M Watson, Sally M Harrison, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|July 6, 2019
Cas9-based enrichment and single-molecule sequencing for precise characterization of genomic duplicationsChristopher M Watson, Laura A Crinnion, Sarah Hewitt, et al.
Surgical Innovation|May 24, 2015
Reducing Accidental Dislodgement of the Percutaneous Endoscopic Gastrostomy: A Prospective Trial of the "SafetyBreak" DeviceLaura H Rosenberger, Christopher A Guidry, John P Davis, et al.
Pageof 10