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Page 1
Detecting DNA cytosine methylation using nanopore sequencing.
Nat Methods. 2017 Apr;14(4):407-410. doi: 10.1038/nmeth.4184. Epub 2017 Feb 20.
Nat Methods. 2017.
PMID: 28218898
GA4GH: International policies and standards for data sharing across genomic research and healthcare.
Rehm HL, Page AJH, Smith L, Adams JB, Alterovitz G, Babb LJ, Barkley MP, Baudis M, Beauvais MJS, Beck T, Beckmann JS, Beltran S, Bernick D, Bernier A, Bonfield JK, Boughtwood TF, Bourque G, Bowers SR, Brookes AJ, Brudno M, Brush MH, Bujold D, Burdett T, Buske OJ, Cabili MN, Cameron DL, Carroll RJ, Casas-Silva E, Chakravarty D, Chaudhari BP, Chen SH, Cherry JM, Chung J, Cline M, Clissold HL, Cook-Deegan RM, Courtot M, Cunningham F, Cupak M, Davies RM, Denisko D, Doerr MJ, Dolman LI, Dove ES, Dursi LJ, Dyke SOM, Eddy JA, Eilbeck K, Ellrott KP, Fairley S, Fakhro KA, Firth HV, Fitzsimons MS, Fiume M, Flicek P, Fore IM, Freeberg MA, Freimuth RR, Fromont LA, Fuerth J, Gaff CL, Gan W, Ghanaim EM, Glazer D, Green RC, Griffith M, Griffith OL, Grossman RL, Groza T, Auvil JMG, Guigó R, Gupta D, Haendel MA, Hamosh A, Hansen DP, Hart RK, Hartley DM, Haussler D, Hendricks-Sturrup RM, Ho CWL, Hobb AE, Hoffman MM, Hofmann OM, Holub P, Hsu JS, Hubaux JP, Hunt SE, Husami A, Jacobsen JO, Jamuar SS, Janes EL, Jeanson F, Jené A, Johns AL, Joly Y, Jones SJM, Kanitz A, Kato K, Keane TM, Kekesi-Lafrance K, Kelleher J, Kerry G, Khor SS, Knoppers BM, Konopko MA, Kosaki K, Kuba M, Lawson J, Leinonen …
See abstract for full author list ➔
Rehm HL, et al. Among authors: dursi lj.
Cell Genom. 2021 Nov 10;1(2):100029. doi: 10.1016/j.xgen.2021.100029.
Cell Genom. 2021.
PMID: 35072136
Free PMC article.
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Retrospective evaluation of whole exome and genome mutation calls in 746 cancer samples.
Bailey MH, Meyerson WU, Dursi LJ, Wang LB, Dong G, Liang WW, Weerasinghe A, Li S, Li Y, Kelso S; MC3 Working Group; PCAWG novel somatic mutation calling methods working group; Saksena G, Ellrott K, Wendl MC, Wheeler DA, Getz G, Simpson JT, Gerstein MB, Ding L; PCAWG Consortium.
Bailey MH, et al. Among authors: dursi lj.
Nat Commun. 2020 Sep 21;11(1):4748. doi: 10.1038/s41467-020-18151-y.
Nat Commun. 2020.
PMID: 32958763
Free PMC article.
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CanDIG: Federated network across Canada for multi-omic and health data discovery and analysis.
Dursi LJ, Bozoky Z, de Borja R, Li H, Bujold D, Lipski A, Rashid SF, Sethi A, Memon N, Naidoo D, Coral-Sasso F, Wong M, Quirion PO, Lu Z, Agarwal S, Pavlov Y, Ponomarev A, Husic M, Pace K, Palmer S, Grover SA, Hakgor S, Siu LL, Malkin D, Virtanen C, Pugh TJ, Jacques PÉ, Joly Y, Jones SJM, Bourque G, Brudno M.
Dursi LJ, et al.
Cell Genom. 2021 Nov 10;1(2):100033. doi: 10.1016/j.xgen.2021.100033. eCollection 2021 Nov 10.
Cell Genom. 2021.
PMID: 36778585
Free PMC article.
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Nanocall: an open source basecaller for Oxford Nanopore sequencing data.
David M, Dursi LJ, Yao D, Boutros PC, Simpson JT.
David M, et al. Among authors: dursi lj.
Bioinformatics. 2017 Jan 1;33(1):49-55. doi: 10.1093/bioinformatics/btw569. Epub 2016 Sep 10.
Bioinformatics. 2017.
PMID: 27614348
Free PMC article.
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Author Correction: Retrospective evaluation of whole exome and genome mutation calls in 746 cancer samples.
Bailey MH, Meyerson WU, Dursi LJ, Wang LB, Dong G, Liang WW, Weerasinghe A, Li S, Li Y, Kelso S; MC3 Working Group; PCAWG novel somatic mutation calling methods working group; Saksena G, Ellrott K, Wendl MC, Wheeler DA, Getz G, Simpson JT, Gerstein MB, Ding L; PCAWG Consortium.
Bailey MH, et al. Among authors: dursi lj.
Nat Commun. 2020 Nov 30;11(1):6232. doi: 10.1038/s41467-020-20128-w.
Nat Commun. 2020.
PMID: 33257764
Free PMC article.
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