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Complex biomarker discovery in neuroimaging data: Finding a needle in a haystack.
Atluri G, Padmanabhan K, Fang G, Steinbach M, Petrella JR, Lim K, Macdonald A 3rd, Samatova NF, Doraiswamy PM, Kumar V. Atluri G, et al. Among authors: fang g. Neuroimage Clin. 2013 Aug 7;3:123-31. doi: 10.1016/j.nicl.2013.07.004. Neuroimage Clin. 2013. PMID: 24179856 Free PMC article. Review.
Genomic variation in myeloma: design, content, and initial application of the Bank On A Cure SNP Panel to detect associations with progression-free survival.
Van Ness B, Ramos C, Haznadar M, Hoering A, Haessler J, Crowley J, Jacobus S, Oken M, Rajkumar V, Greipp P, Barlogie B, Durie B, Katz M, Atluri G, Fang G, Gupta R, Steinbach M, Kumar V, Mushlin R, Johnson D, Morgan G. Van Ness B, et al. Among authors: fang g. BMC Med. 2008 Sep 8;6:26. doi: 10.1186/1741-7015-6-26. BMC Med. 2008. PMID: 18778477 Free PMC article.
Genome-wide mapping of methylated adenine residues in pathogenic Escherichia coli using single-molecule real-time sequencing.
Fang G, Munera D, Friedman DI, Mandlik A, Chao MC, Banerjee O, Feng Z, Losic B, Mahajan MC, Jabado OJ, Deikus G, Clark TA, Luong K, Murray IA, Davis BM, Keren-Paz A, Chess A, Roberts RJ, Korlach J, Turner SW, Kumar V, Waldor MK, Schadt EE. Fang G, et al. Nat Biotechnol. 2012 Dec;30(12):1232-9. doi: 10.1038/nbt.2432. Epub 2012 Nov 8. Nat Biotechnol. 2012. PMID: 23138224 Free PMC article.
Modeling kinetic rate variation in third generation DNA sequencing data to detect putative modifications to DNA bases.
Schadt EE, Banerjee O, Fang G, Feng Z, Wong WH, Zhang X, Kislyuk A, Clark TA, Luong K, Keren-Paz A, Chess A, Kumar V, Chen-Plotkin A, Sondheimer N, Korlach J, Kasarskis A. Schadt EE, et al. Among authors: fang g. Genome Res. 2013 Jan;23(1):129-41. doi: 10.1101/gr.136739.111. Epub 2012 Oct 23. Genome Res. 2013. PMID: 23093720 Free PMC article.
1,904 results