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Hannah Kelly

Showing results (31-40 of 46) with videos related to

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Forensic Science International. Genetics|November 16, 2020
Estimating the number of contributors to a DNA profile using decision treesMaarten Kruijver, Hannah Kelly, Kevin Cheng, et al.
Forensic Science International. Genetics|February 15, 2021
Validation of a top-down DNA profile analysis for database searching using a fully continuous probabilistic genotyping modelDuncan Taylor, Jo-Anne Bright, Lenara Scandrett, et al.
The Journal of Clinical Endocrinology and Metabolism|January 4, 2007
Analysis of the Fc receptor-like-3 (FCRL3) locus in Caucasians with autoimmune disorders suggests a complex pattern of disease associationCatherine J Owen, Hannah Kelly, James A Eden, et al.
Journal of Forensic Sciences|September 27, 2023
A diagnosis of the primary difference between EuroForMix and STRmix™John Buckleton, Mateusz Susik, James M Curran, et al.
Cureus|February 2, 2024
Recognition of Significantly Delayed Spinal Cord Ischemia Following Thoracic Endovascular Aortic Repair: A Case Report and Review of the LiteratureHannah Kelly, Danielle Herman, Kiana Loo, et al.
Forensic Science International. Genetics|November 12, 2022
Developmental validation of STRmix™ NGS, a probabilistic genotyping tool for the interpretation of autosomal STRs from forensic profiles generated using NGSKevin Cheng, Jo-Anne Bright, Hannah Kelly, et al.
Concussion (London, England)|April 9, 2020
Vertical smooth pursuit as a diagnostic marker of traumatic brain injuryMelissa Hunfalvay, Claire-Marie Roberts, Nicholas P Murray, et al.
Forensic Science International. Genetics|May 5, 2018
A sensitivity analysis to determine the robustness of STRmix™ with respect to laboratory calibrationHannah Kelly, Jo-Anne Bright, Maarten Kruijver, et al.
Forensic Science International. Genetics|July 19, 2020
Variability and additivity of read counts for aSTRs in NGS DNA profilesKevin Cheng, Jessica Skillman, Stephanie Hickey, et al.
Prenatal Diagnosis|April 6, 2023
Single gene non-invasive prenatal screening for autosomal dominant conditions in a high-risk cohortSophie Adams, Hannah Llorin, Olivia Maher, et al.
Pageof 5

Showing results (31-40 of 46) with videos related to

Sort By:
Pageof 5
Forensic Science International. Genetics|November 16, 2020
Estimating the number of contributors to a DNA profile using decision treesMaarten Kruijver, Hannah Kelly, Kevin Cheng, et al.
Forensic Science International. Genetics|February 15, 2021
Validation of a top-down DNA profile analysis for database searching using a fully continuous probabilistic genotyping modelDuncan Taylor, Jo-Anne Bright, Lenara Scandrett, et al.
The Journal of Clinical Endocrinology and Metabolism|January 4, 2007
Analysis of the Fc receptor-like-3 (FCRL3) locus in Caucasians with autoimmune disorders suggests a complex pattern of disease associationCatherine J Owen, Hannah Kelly, James A Eden, et al.
Journal of Forensic Sciences|September 27, 2023
A diagnosis of the primary difference between EuroForMix and STRmix™John Buckleton, Mateusz Susik, James M Curran, et al.
Cureus|February 2, 2024
Recognition of Significantly Delayed Spinal Cord Ischemia Following Thoracic Endovascular Aortic Repair: A Case Report and Review of the LiteratureHannah Kelly, Danielle Herman, Kiana Loo, et al.
Forensic Science International. Genetics|November 12, 2022
Developmental validation of STRmix™ NGS, a probabilistic genotyping tool for the interpretation of autosomal STRs from forensic profiles generated using NGSKevin Cheng, Jo-Anne Bright, Hannah Kelly, et al.
Concussion (London, England)|April 9, 2020
Vertical smooth pursuit as a diagnostic marker of traumatic brain injuryMelissa Hunfalvay, Claire-Marie Roberts, Nicholas P Murray, et al.
Forensic Science International. Genetics|May 5, 2018
A sensitivity analysis to determine the robustness of STRmix™ with respect to laboratory calibrationHannah Kelly, Jo-Anne Bright, Maarten Kruijver, et al.
Forensic Science International. Genetics|July 19, 2020
Variability and additivity of read counts for aSTRs in NGS DNA profilesKevin Cheng, Jessica Skillman, Stephanie Hickey, et al.
Prenatal Diagnosis|April 6, 2023
Single gene non-invasive prenatal screening for autosomal dominant conditions in a high-risk cohortSophie Adams, Hannah Llorin, Olivia Maher, et al.
Pageof 5