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Analytical Validation of Clinical Whole-Genome and Transcriptome Sequencing of Patient-Derived Tumors for Reporting Targetable Variants in Cancer.
Wrzeszczynski KO, Felice V, Abhyankar A, Kozon L, Geiger H, Manaa D, London F, Robinson D, Fang X, Lin D, Lamendola-Essel MF, Khaira D, Dikoglu E, Emde AK, Robine N, Shah M, Arora K, Basturk O, Bhanot U, Kentsis A, Mansukhani MM, Bhagat G, Jobanputra V. Wrzeszczynski KO, et al. Among authors: kozon l. J Mol Diagn. 2018 Nov;20(6):822-835. doi: 10.1016/j.jmoldx.2018.06.007. Epub 2018 Aug 21. J Mol Diagn. 2018. PMID: 30138725 Free PMC article.
Detection of Copy Number Variants by Short Multiply Aggregated Sequence Homologies.
Jobanputra V, Andrews P, Felice V, Abhyankar A, Kozon L, Robinson D, London F, Hakker I, Wrzeszczynski K, Ronemus M. Jobanputra V, et al. Among authors: kozon l. J Mol Diagn. 2020 Dec;22(12):1476-1481. doi: 10.1016/j.jmoldx.2020.09.009. Epub 2020 Oct 23. J Mol Diagn. 2020. PMID: 33132082 Free PMC article.