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Bioinformatics (Oxford, England)|April 18, 2019
Spliceogen: an integrative, scalable tool for the discovery of splice-altering variantsSteven Monger, Michael Troup, Eddie Ip, et al.Briefings in Bioinformatics|November 8, 2025
Systematic evaluation of de novo mutation calling tools using whole genome sequencing dataAnushi Shah, Steven Monger, Michael Troup, et al.RNA Biology|September 23, 2020
Transposon clusters as substrates for aberrant splice-site activationMaria Elena Vilar Alvarez, Martin Chivers, Ivana Borovska, et al.Bioinformatics Advances|November 4, 2025
Benchmarking of variant pathogenicity prediction methods using a population genetics approachMikhail Gudkov, Loïc Thibaut, Steven Monger, et al.Human Molecular Genetics|December 10, 2019
Functional genomics and gene-environment interaction highlight the complexity of congenital heart disease caused by Notch pathway variantsGavin Chapman, Julie L M Moreau, Eddie I P, et al.Circulation. Genomic and Precision Medicine|May 18, 2022
Exploring the Genetic Architecture of Spontaneous Coronary Artery Dissection Using Whole-Genome SequencingIngrid Tarr, Stephanie Hesselson, Siiri E Iismaa, et al.Pageof 1