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Cancer Cell|February 16, 2013
Breaking news on fragile sites in cancerThomas W Glover, Thomas E Wilson
Mutation Research. Reviews in Mutation Research|November 6, 2023
Applications of advanced technologies for detecting genomic structural variationVincent A Laufer, Thomas W Glover, Thomas E Wilson
Nature Reviews. Cancer|July 26, 2017
Fragile sites in cancer: more than meets the eyeThomas W Glover, Thomas E Wilson, Martin F Arlt
Current Opinion in Genetics & Development|February 28, 2012
Replication stress and mechanisms of CNV formationMartin F Arlt, Thomas E Wilson, Thomas W Glover
Nature Communications|November 6, 2024
Replication stress induces POLQ-mediated structural variant formation throughout common fragile sites after entry into mitosisThomas E Wilson, Samreen Ahmed, Amanda Winningham, et al.
NAR Genomics and Bioinformatics|May 14, 2023
svCapture: efficient and specific detection of very low frequency structural variant junctions by error-minimized capture sequencingThomas E Wilson, Samreen Ahmed, Jake Higgins, et al.
Environmental and Molecular Mutagenesis|December 12, 2013
Copy number variants are produced in response to low-dose ionizing radiation in cultured cellsMartin F Arlt, Sountharia Rajendran, Shanda R Birkeland, et al.
Plos Genetics|October 3, 2012
De novo CNV formation in mouse embryonic stem cells occurs in the absence of Xrcc4-dependent nonhomologous end joiningMartin F Arlt, Sountharia Rajendran, Shanda R Birkeland, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 12, 2011
Hydroxyurea induces de novo copy number variants in human cellsMartin F Arlt, Alev Cagla Ozdemir, Shanda R Birkeland, et al.
Biorxiv : the Preprint Server for Biology|July 10, 2026
High-fidelity rare structural variant detection with HiFiRE3 reduced representation via restriction enzyme endsJoseph A Stewart, Jeanmarie Mishler, Samreen Ahmed, et al.
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