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tHapMix: simulating tumour samples through haplotype mixtures.
Ivakhno S, Colombo C, Tanner S, Tedder P, Berri S, Cox AJ. Ivakhno S, et al. Among authors: tanner s. Bioinformatics. 2017 Jan 15;33(2):280-282. doi: 10.1093/bioinformatics/btw589. Epub 2016 Sep 7. Bioinformatics. 2017. PMID: 27605106
Copy-number variants in clinical genome sequencing: deployment and interpretation for rare and undiagnosed disease.
Gross AM, Ajay SS, Rajan V, Brown C, Bluske K, Burns NJ, Chawla A, Coffey AJ, Malhotra A, Scocchia A, Thorpe E, Dzidic N, Hovanes K, Sahoo T, Dolzhenko E, Lajoie B, Khouzam A, Chowdhury S, Belmont J, Roller E, Ivakhno S, Tanner S, McEachern J, Hambuch T, Eberle M, Hagelstrom RT, Bentley DR, Perry DL, Taft RJ. Gross AM, et al. Among authors: tanner s. Genet Med. 2019 May;21(5):1121-1130. doi: 10.1038/s41436-018-0295-y. Epub 2018 Oct 8. Genet Med. 2019. PMID: 30293986 Free PMC article.
Isaac: ultra-fast whole-genome secondary analysis on Illumina sequencing platforms.
Raczy C, Petrovski R, Saunders CT, Chorny I, Kruglyak S, Margulies EH, Chuang HY, Källberg M, Kumar SA, Liao A, Little KM, Strömberg MP, Tanner SW. Raczy C, et al. Among authors: tanner sw. Bioinformatics. 2013 Aug 15;29(16):2041-3. doi: 10.1093/bioinformatics/btt314. Epub 2013 Jun 4. Bioinformatics. 2013. PMID: 23736529
Improving gene annotation using peptide mass spectrometry.
Tanner S, Shen Z, Ng J, Florea L, Guigó R, Briggs SP, Bafna V. Tanner S, et al. Genome Res. 2007 Feb;17(2):231-9. doi: 10.1101/gr.5646507. Epub 2006 Dec 22. Genome Res. 2007. PMID: 17189379 Free PMC article.
579 results