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BMC Bioinformatics|June 6, 2020
Origins and characterization of variants shared between databases of somatic and germline human mutationsWilliam Meyerson, John Leisman, Fabio C P Navarro, et al.
Bioinformatics (Oxford, England)|July 30, 2020
FANCY: fast estimation of privacy risk in functional genomics dataGamze Gürsoy, Charlotte M Brannon, Fabio C P Navarro, et al.
Plos Genetics|January 30, 2013
Gene copy-number polymorphism caused by retrotransposition in humansDaniel R Schrider, Fabio C P Navarro, Pedro A F Galante, et al.
Nucleic Acids Research|December 21, 2020
To mock or not: a comprehensive comparison of mock IP and DNA input for ChIP-seqJinrui Xu, Michelle M Kudron, Alec Victorsen, et al.
Cancer Research|May 28, 2021
STK11/LKB1 Loss of Function Is Associated with Global DNA Hypomethylation and S-Adenosyl-Methionine Depletion in Human Lung AdenocarcinomaMichael J Koenig, Bernice A Agana, Jacob M Kaufman, et al.
Genome Biology|March 22, 2018
FusorSV: an algorithm for optimally combining data from multiple structural variation detection methodsTimothy Becker, Wan-Ping Lee, Joseph Leone, et al.
Nature Communications|April 27, 2016
Diverse human extracellular RNAs are widely detected in human plasmaJane E Freedman, Mark Gerstein, Eric Mick, et al.
Oncotarget|September 7, 2014
Mutational analysis of genes coding for cell surface proteins in colorectal cancer cell lines reveal novel altered pathways, druggable mutations and mutated epitopes for targeted therapyElisa Donnard, Paula F Asprino, Bruna R Correa, et al.
Oncotarget|May 24, 2017
High IL-1R8 expression in breast tumors promotes tumor growth and contributes to impaired antitumor immunityLuis Felipe Campesato, Ana Paula M Silva, Luna Cordeiro, et al.
Oncotarget|March 14, 2024
Analytical validation of NeXT Personal®, an ultra-sensitive personalized circulating tumor DNA assayJosette Northcott, Gabor Bartha, Jason Harris, et al.
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