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Journal of Biomedicine & Biotechnology|July 14, 2010
Semi-automated library preparation for high-throughput DNA sequencing platformsEveline Farias-Hesson, Jonathan Erikson, Alexander Atkins, et al.
Molecular Genetics and Metabolism|October 17, 2022
Metabolic diversity in human populations and correlation with genetic and ancestral geographic distancesGang Peng, Andrew J Pakstis, Neeru Gandotra, et al.
Forensic Science International. Genetics|April 20, 2020
Validation of novel forensic DNA markers using multiplex microhaplotype sequencingNeeru Gandotra, William C Speed, Wenyi Qin, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 29, 2020
Massively parallel discovery of human-specific substitutions that alter enhancer activitySeverin Uebbing, Jake Gockley, Steven K Reilly, et al.
International Journal of Neonatal Screening|November 21, 2023
NBSTRN Tools to Advance Newborn Screening Research and Support Newborn Screening StakeholdersKee Chan, Zhanzhi Hu, Lynn W Bush, et al.
Science Advances|September 6, 2023
Digital assay for rapid electronic quantification of clinical pathogens using DNA nanoballsMuhammad Tayyab, Donal Barrett, Gijs van Riel, et al.
BMC Genomics|April 9, 2014
A functional screen for copper homeostasis genes identifies a pharmacologically tractable cellular systemUlrich Schlecht, Sundari Suresh, Weihong Xu, et al.
Journal of Cardiovascular Translational Research|February 5, 2026
PAD-associated Genetic Variants are More Strongly Associated with Surgical Intervention than Premature OnsetJiaqi Hu, Dana Alameddine, He Wang, et al.
Frontiers in Genetics|December 19, 2025
Perspectives of parents receiving normal results from genomic newborn screening: a mixed-methods evaluation from the early check programAngela Y Gwaltney, Sean N Halpin, Samantha Scott, et al.
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