129 related articles for article (PubMed ID: 37683892)
41. Characterization of Fecal Microbiota with Clinical Specimen Using Long-Read and Short-Read Sequencing Platform.
Wei PL; Hung CS; Kao YW; Lin YC; Lee CY; Chang TH; Shia BC; Lin JC
Int J Mol Sci; 2020 Sep; 21(19):. PubMed ID: 32993155
[TBL] [Abstract][Full Text] [Related]
42. Approaches to Whole Mitochondrial Genome Sequencing on the Oxford Nanopore MinION.
Zascavage RR; Hall CL; Thorson K; Mahmoud M; Sedlazeck FJ; Planz JV
Curr Protoc Hum Genet; 2019 Dec; 104(1):e94. PubMed ID: 31743587
[TBL] [Abstract][Full Text] [Related]
43. Draft genome assemblies using sequencing reads from Oxford Nanopore Technology and Illumina platforms for four species of North American Fundulus killifish.
Johnson LK; Sahasrabudhe R; Gill JA; Roach JL; Froenicke L; Brown CT; Whitehead A
Gigascience; 2020 Jun; 9(6):. PubMed ID: 32556169
[TBL] [Abstract][Full Text] [Related]
44. De novo assembly of the Indian blue peacock (Pavo cristatus) genome using Oxford Nanopore technology and Illumina sequencing.
Dhar R; Seethy A; Pethusamy K; Singh S; Rohil V; Purkayastha K; Mukherjee I; Goswami S; Singh R; Raj A; Srivastava T; Acharya S; Rajashekhar B; Karmakar S
Gigascience; 2019 May; 8(5):. PubMed ID: 31077316
[TBL] [Abstract][Full Text] [Related]
45. NanoSim: nanopore sequence read simulator based on statistical characterization.
Yang C; Chu J; Warren RL; Birol I
Gigascience; 2017 Apr; 6(4):1-6. PubMed ID: 28327957
[TBL] [Abstract][Full Text] [Related]
46. Structural variant analysis of a cancer reference cell line sample using multiple sequencing technologies.
Talsania K; Shen TW; Chen X; Jaeger E; Li Z; Chen Z; Chen W; Tran B; Kusko R; Wang L; Pang AWC; Yang Z; Choudhari S; Colgan M; Fang LT; Carroll A; Shetty J; Kriga Y; German O; Smirnova T; Liu T; Li J; Kellman B; Hong K; Hastie AR; Natarajan A; Moshrefi A; Granat A; Truong T; Bombardi R; Mankinen V; Meerzaman D; Mason CE; Collins J; Stahlberg E; Xiao C; Wang C; Xiao W; Zhao Y
Genome Biol; 2022 Dec; 23(1):255. PubMed ID: 36514120
[TBL] [Abstract][Full Text] [Related]
47. Oxford Nanopore sequencing: new opportunities for plant genomics?
Dumschott K; Schmidt MH; Chawla HS; Snowdon R; Usadel B
J Exp Bot; 2020 Sep; 71(18):5313-5322. PubMed ID: 32459850
[TBL] [Abstract][Full Text] [Related]
48. Longshot enables accurate variant calling in diploid genomes from single-molecule long read sequencing.
Edge P; Bansal V
Nat Commun; 2019 Oct; 10(1):4660. PubMed ID: 31604920
[TBL] [Abstract][Full Text] [Related]
49. Nanopore Long Read DNA Sequencing of Protozoan Parasites: Hybrid Genome Assembly of Trypanosoma cruzi.
Díaz-Viraqué F; Greif G; Berná L; Robello C
Methods Mol Biol; 2021; 2369():3-13. PubMed ID: 34313980
[TBL] [Abstract][Full Text] [Related]
50. Comprehensive analysis of structural variants in breast cancer genomes using single-molecule sequencing.
Aganezov S; Goodwin S; Sherman RM; Sedlazeck FJ; Arun G; Bhatia S; Lee I; Kirsche M; Wappel R; Kramer M; Kostroff K; Spector DL; Timp W; McCombie WR; Schatz MC
Genome Res; 2020 Sep; 30(9):1258-1273. PubMed ID: 32887686
[TBL] [Abstract][Full Text] [Related]
51. 1D Genome Sequencing on the Oxford Nanopore MinION.
Goodwin S; Wappel R; McCombie WR
Curr Protoc Hum Genet; 2017 Jul; 94():18.11.1-18.11.14. PubMed ID: 28696556
[TBL] [Abstract][Full Text] [Related]
52. Analyses of breakpoint junctions of complex genomic rearrangements comprising multiple consecutive microdeletions by nanopore sequencing.
Imaizumi T; Yamamoto-Shimojima K; Yanagishita T; Ondo Y; Yamamoto T
J Hum Genet; 2020 Sep; 65(9):735-741. PubMed ID: 32355308
[TBL] [Abstract][Full Text] [Related]
53. Long-read sequencing for reliably calling the
Krøvel AV; Hetland MAK; Bernhoff E; Bjørheim AS; Soma MA; Löhr IH
Front Cell Infect Microbiol; 2023; 13():1176182. PubMed ID: 37256104
[TBL] [Abstract][Full Text] [Related]
54. Comparison of long-read sequencing technologies in the hybrid assembly of complex bacterial genomes.
De Maio N; Shaw LP; Hubbard A; George S; Sanderson ND; Swann J; Wick R; AbuOun M; Stubberfield E; Hoosdally SJ; Crook DW; Peto TEA; Sheppard AE; Bailey MJ; Read DS; Anjum MF; Walker AS; Stoesser N; On Behalf Of The Rehab Consortium
Microb Genom; 2019 Sep; 5(9):. PubMed ID: 31483244
[TBL] [Abstract][Full Text] [Related]
55. DNA isolation methods for Nanopore sequencing of the
Pinzauti D; Iannelli F; Pozzi G; Santoro F
Microb Genom; 2022 Feb; 8(2):. PubMed ID: 35171093
[No Abstract] [Full Text] [Related]
56. Diagnosis of copy number variation by Illumina next generation sequencing is comparable in performance to oligonucleotide array comparative genomic hybridisation.
Hayes JL; Tzika A; Thygesen H; Berri S; Wood HM; Hewitt S; Pendlebury M; Coates A; Willoughby L; Watson CM; Rabbitts P; Roberts P; Taylor GR
Genomics; 2013 Sep; 102(3):174-81. PubMed ID: 23598253
[TBL] [Abstract][Full Text] [Related]
57. Benchmarking hybrid assembly approaches for genomic analyses of bacterial pathogens using Illumina and Oxford Nanopore sequencing.
Chen Z; Erickson DL; Meng J
BMC Genomics; 2020 Sep; 21(1):631. PubMed ID: 32928108
[TBL] [Abstract][Full Text] [Related]
58. Whole human genome 5'-mC methylation analysis using long read nanopore sequencing.
Silva C; Machado M; Ferrão J; Sebastião Rodrigues A; Vieira L
Epigenetics; 2022 Dec; 17(13):1961-1975. PubMed ID: 35856633
[TBL] [Abstract][Full Text] [Related]
59. Rapid, multiplexed, whole genome and plasmid sequencing of foodborne pathogens using long-read nanopore technology.
Taylor TL; Volkening JD; DeJesus E; Simmons M; Dimitrov KM; Tillman GE; Suarez DL; Afonso CL
Sci Rep; 2019 Nov; 9(1):16350. PubMed ID: 31704961
[TBL] [Abstract][Full Text] [Related]
60. Assessment of low-coverage nanopore long read sequencing for SNP genotyping in doubled haploid canola (Brassica napus L.).
Malmberg MM; Spangenberg GC; Daetwyler HD; Cogan NOI
Sci Rep; 2019 Jun; 9(1):8688. PubMed ID: 31213642
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]