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Cytogenetic and Genome Research|August 31, 2017
Genomic and Cytogenetic Characterization of a Balanced Translocation Disrupting NUP98My Linh Thibodeau, Michelle Steinraths, Lindsay Brown, et al.
Bioinformatics (Oxford, England)|July 18, 2018
MAVIS: merging, annotation, validation, and illustration of structural variantsCaralyn Reisle, Karen L Mungall, Caleb Choo, et al.
Oncotarget|November 8, 2012
Recurrent targets of aberrant somatic hypermutation in lymphomaAlireza Hadj Khodabakhshi, Ryan D Morin, Anthony P Fejes, et al.
Bioinformatics (Oxford, England)|May 8, 2012
BreakFusion: targeted assembly-based identification of gene fusions in whole transcriptome paired-end sequencing dataKen Chen, John W Wallis, Cyriac Kandoth, et al.
Blood|April 13, 2012
TBL1XR1/TP63: a novel recurrent gene fusion in B-cell non-Hodgkin lymphomaDavid W Scott, Karen L Mungall, Susana Ben-Neriah, et al.
Briefings in Bioinformatics|September 10, 2024
Enhancing clinical genomic accuracy with panelGC: a novel metric and tool for quantifying and monitoring GC biases in hybridization capture panel sequencingXuanjin Cheng, Murathan T Goktas, Laura M Williamson, et al.
Biotechniques|August 8, 2023
A high-throughput pipeline for DNA/RNA/small RNA purification from tissue samples for sequencingJing Xu, Pawan K Pandoh, Richard D Corbett, et al.
European Journal of Human Genetics : EJHG|February 16, 2023
Defining the heterogeneity of unbalanced structural variation underlying breast cancer susceptibility by nanopore genome sequencingKatherine Dixon, Yaoqing Shen, Kieran O'Neill, et al.
Frontiers in Genetics|December 17, 2024
Adaptable and comprehensive approaches for long-read nanopore sequencing of polyadenylated and non-polyadenylated RNAsSimon Haile, Richard D Corbett, Kieran O'Neill, et al.
Cold Spring Harbor Molecular Case Studies|June 5, 2019
Genomic characterization of a well-differentiated grade 3 pancreatic neuroendocrine tumorLaura M Williamson, Michael Steel, Jasleen K Grewal, et al.
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