Updating benchtop sequencing performance comparison
Jünemann S, Sedlazeck FJ, Prior K, Albersmeier A, John U, Kalinowski J, Mellmann A, Goesmann A, von Haeseler A, Stoye J, Harmsen D (2013)
Nature Biotechnology 31(4): 294-296.
Zeitschriftenaufsatz
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Autor*in
Jünemann, SebastianUniBi;
Sedlazeck, Fritz Joachim;
Prior, Karola;
Albersmeier, AndreasUniBi;
John, Uwe;
Kalinowski, JörnUniBi;
Mellmann, Alexander;
Goesmann, AlexanderUniBi ;
von Haeseler, Arndt;
Stoye, JensUniBi ;
Harmsen, Dag
Einrichtung
Centrum für Biotechnologie > Arbeitsgruppe J. Kalinowski
Centrum für Biotechnologie > Arbeitsgruppe A. Goesmann
Technische Fakultät > AG Genominformatik
Centrum für Biotechnologie > Arbeitsgruppe J. Stoye
Centrum für Biotechnologie > Institut für Bioinformatik
Centrum für Biotechnologie > Institut für Genomforschung und Systembiologie
Technische Fakultät > Computational Genomics
Centrum für Biotechnologie > Arbeitsgruppe A. Goesmann
Technische Fakultät > AG Genominformatik
Centrum für Biotechnologie > Arbeitsgruppe J. Stoye
Centrum für Biotechnologie > Institut für Bioinformatik
Centrum für Biotechnologie > Institut für Genomforschung und Systembiologie
Technische Fakultät > Computational Genomics
Erscheinungsjahr
2013
Zeitschriftentitel
Nature Biotechnology
Band
31
Ausgabe
4
Seite(n)
294-296
ISSN
1087-0156
eISSN
1546-1696
Page URI
https://pub.uni-bielefeld.de/record/2566922
Zitieren
Jünemann S, Sedlazeck FJ, Prior K, et al. Updating benchtop sequencing performance comparison. Nature Biotechnology. 2013;31(4):294-296.
Jünemann, S., Sedlazeck, F. J., Prior, K., Albersmeier, A., John, U., Kalinowski, J., Mellmann, A., et al. (2013). Updating benchtop sequencing performance comparison. Nature Biotechnology, 31(4), 294-296. doi:10.1038/nbt.2522
Jünemann, Sebastian, Sedlazeck, Fritz Joachim, Prior, Karola, Albersmeier, Andreas, John, Uwe, Kalinowski, Jörn, Mellmann, Alexander, et al. 2013. “Updating benchtop sequencing performance comparison”. Nature Biotechnology 31 (4): 294-296.
Jünemann, S., Sedlazeck, F. J., Prior, K., Albersmeier, A., John, U., Kalinowski, J., Mellmann, A., Goesmann, A., von Haeseler, A., Stoye, J., et al. (2013). Updating benchtop sequencing performance comparison. Nature Biotechnology 31, 294-296.
Jünemann, S., et al., 2013. Updating benchtop sequencing performance comparison. Nature Biotechnology, 31(4), p 294-296.
S. Jünemann, et al., “Updating benchtop sequencing performance comparison”, Nature Biotechnology, vol. 31, 2013, pp. 294-296.
Jünemann, S., Sedlazeck, F.J., Prior, K., Albersmeier, A., John, U., Kalinowski, J., Mellmann, A., Goesmann, A., von Haeseler, A., Stoye, J., Harmsen, D.: Updating benchtop sequencing performance comparison. Nature Biotechnology. 31, 294-296 (2013).
Jünemann, Sebastian, Sedlazeck, Fritz Joachim, Prior, Karola, Albersmeier, Andreas, John, Uwe, Kalinowski, Jörn, Mellmann, Alexander, Goesmann, Alexander, von Haeseler, Arndt, Stoye, Jens, and Harmsen, Dag. “Updating benchtop sequencing performance comparison”. Nature Biotechnology 31.4 (2013): 294-296.
Daten bereitgestellt von European Bioinformatics Institute (EBI)
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Castelhano Santos N, Pereira MO, Lourenço A., Brief Bioinform 16(1), 2015
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Deng X, Shariat N, Driebe EM, Roe CC, Tolar B, Trees E, Keim P, Zhang W, Dudley EG, Fields PI, Engelthaler DM., J Clin Microbiol 53(1), 2015
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Comparing High-throughput Platforms for Sequencing the V4 Region of SSU-rDNA in Environmental Microbial Eukaryotic Diversity Surveys.
Mahé F, Mayor J, Bunge J, Chi J, Siemensmeyer T, Stoeck T, Wahl B, Paprotka T, Filker S, Dunthorn M., J Eukaryot Microbiol 62(3), 2015
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Hamakawa T, Kukita Y, Kurokawa Y, Miyazaki Y, Takahashi T, Yamasaki M, Miyata H, Nakajima K, Taniguchi K, Takiguchi S, Mori M, Doki Y, Kato K., Br J Cancer 112(2), 2015
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Hamakawa T, Kukita Y, Kurokawa Y, Miyazaki Y, Takahashi T, Yamasaki M, Miyata H, Nakajima K, Taniguchi K, Takiguchi S, Mori M, Doki Y, Kato K., Br J Cancer 112(2), 2015
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Mutational profiling of therapy-related myelodysplastic syndromes and acute myeloid leukemia by next generation sequencing, a comparison with de novo diseases.
Ok CY, Patel KP, Garcia-Manero G, Routbort MJ, Fu B, Tang G, Goswami M, Singh R, Kanagal-Shamanna R, Pierce SA, Young KH, Kantarjian HM, Medeiros LJ, Luthra R, Wang SA., Leuk Res 39(3), 2015
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Robilotti E, Kamboj M., J Clin Microbiol 53(4), 2015
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Van den Hoecke S, Verhelst J, Vuylsteke M, Saelens X., BMC Genomics 16(), 2015
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Rusu LI, Wyres KL, Reumann M, Queiroz C, Bojovschi A, Conway T, Garg S, Edwards DJ, Hogg G, Holt KE., Health Inf Sci Syst 3(suppl 1 hisa big data in biomedicine and healthcare 201), 2015
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Rusu LI, Wyres KL, Reumann M, Queiroz C, Bojovschi A, Conway T, Garg S, Edwards DJ, Hogg G, Holt KE., Health Inf Sci Syst 3(suppl 1 hisa big data in biomedicine and healthcare 201), 2015
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Hirotsu Y, Kanda T, Matsumura H, Moriyama M, Yokosuka O, Omata M., Hepatol Int 9(3), 2015
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May A, Abeln S, Buijs MJ, Heringa J, Crielaard W, Brandt BW., Nucleic Acids Res 43(w1), 2015
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Maslov AY, Quispe-Tintaya W, Gorbacheva T, White RR, Vijg J., Mutat Res 776(), 2015
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Evaluation of the Ion Torrent Personal Genome Machine for Gene-Targeted Studies Using Amplicons of the Nitrogenase Gene nifH.
Zhang B, Penton CR, Xue C, Wang Q, Zheng T, Tiedje JM., Appl Environ Microbiol 81(13), 2015
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TP53 mutation characteristics in therapy-related myelodysplastic syndromes and acute myeloid leukemia is similar to de novo diseases.
Ok CY, Patel KP, Garcia-Manero G, Routbort MJ, Peng J, Tang G, Goswami M, Young KH, Singh R, Medeiros LJ, Kantarjian HM, Luthra R, Wang SA., J Hematol Oncol 8(), 2015
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High-Throughput, Amplicon-Based Sequencing of the CREBBP Gene as a Tool to Develop a Universal Platform-Independent Assay.
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High-fidelity target sequencing of individual molecules identified using barcode sequences: de novo detection and absolute quantitation of mutations in plasma cell-free DNA from cancer patients.
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Whole-genome sequencing in outbreak analysis.
Gilchrist CA, Turner SD, Riley MF, Petri WA, Hewlett EL., Clin Microbiol Rev 28(3), 2015
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Defining and Evaluating a Core Genome Multilocus Sequence Typing Scheme for Whole-Genome Sequence-Based Typing of Listeria monocytogenes.
Ruppitsch W, Pietzka A, Prior K, Bletz S, Fernandez HL, Allerberger F, Harmsen D, Mellmann A., J Clin Microbiol 53(9), 2015
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Utility of Whole-Genome Sequencing of Escherichia coli O157 for Outbreak Detection and Epidemiological Surveillance.
Holmes A, Allison L, Ward M, Dallman TJ, Clark R, Fawkes A, Murphy L, Hanson M., J Clin Microbiol 53(11), 2015
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Introduction to the analysis of next generation sequencing data and its application to venous thromboembolism.
Cunha ML, Meijers JC, Middeldorp S., Thromb Haemost 114(5), 2015
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Tapia E, Spetale F, Krsticevic F, Angelone L, Bulacio P., PLoS One 10(10), 2015
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Quasispecies Analyses of the HIV-1 Near-full-length Genome With Illumina MiSeq.
Ode H, Matsuda M, Matsuoka K, Hachiya A, Hattori J, Kito Y, Yokomaku Y, Iwatani Y, Sugiura W., Front Microbiol 6(), 2015
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Evaluation and Validation of Assembling Corrected PacBio Long Reads for Microbial Genome Completion via Hybrid Approaches.
Lin HH, Liao YC., PLoS One 10(12), 2015
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Next-generation sequencing-based multigene mutational screening for acute myeloid leukemia using MiSeq: applicability for diagnostics and disease monitoring.
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Bacterial whole-genome sequencing revisited: portable, scalable, and standardized analysis for typing and detection of virulence and antibiotic resistance genes.
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OTG-snpcaller: an optimized pipeline based on TMAP and GATK for SNP calling from ion torrent data.
Zhu P, He L, Li Y, Huang W, Xi F, Lin L, Zhi Q, Zhang W, Tang YT, Geng C, Lu Z, Xu X., PLoS One 9(5), 2014
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Analysis of plant microbe interactions in the era of next generation sequencing technologies.
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High-quality and high-throughput massively parallel sequencing of the human mitochondrial genome using the Illumina MiSeq.
King JL, LaRue BL, Novroski NM, Stoljarova M, Seo SB, Zeng X, Warshauer DH, Davis CP, Parson W, Sajantila A, Budowle B., Forensic Sci Int Genet 12(), 2014
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WGS Analysis and Interpretation in Clinical and Public Health Microbiology Laboratories: What Are the Requirements and How Do Existing Tools Compare?
Wyres KL, Conway TC, Garg S, Queiroz C, Reumann M, Holt K, Rusu LI., Pathogens 3(2), 2014
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Evaluation and optimisation of indel detection workflows for ion torrent sequencing of the BRCA1 and BRCA2 genes.
Yeo ZX, Wong JC, Rozen SG, Lee AS., BMC Genomics 15(), 2014
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Screening and genetic characterization of thermo-tolerant Synechocystis sp. PCC6803 strains created by adaptive evolution.
Tillich UM, Wolter N, Franke P, Dühring U, Frohme M., BMC Biotechnol 14(), 2014
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Validation of high throughput sequencing and microbial forensics applications.
Budowle B, Connell ND, Bielecka-Oder A, Colwell RR, Corbett CR, Fletcher J, Forsman M, Kadavy DR, Markotic A, Morse SA, Murch RS, Sajantila A, Schmedes SE, Ternus KL, Turner SD, Minot S., Investig Genet 5(), 2014
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Cost-efficient HIV-1 drug resistance surveillance using multiplexed high-throughput amplicon sequencing: implications for use in low- and middle-income countries.
Ekici H, Rao SD, Sönnerborg A, Ramprasad VL, Gupta R, Neogi U., J Antimicrob Chemother 69(12), 2014
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Ekici H, Rao SD, Sönnerborg A, Ramprasad VL, Gupta R, Neogi U., J Antimicrob Chemother 69(12), 2014
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Efficient CRISPR-Cas9-mediated genome editing in Plasmodium falciparum.
Wagner JC, Platt RJ, Goldfless SJ, Zhang F, Niles JC., Nat Methods 11(9), 2014
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Solving the problem of comparing whole bacterial genomes across different sequencing platforms.
Kaas RS, Leekitcharoenphon P, Aarestrup FM, Lund O., PLoS One 9(8), 2014
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GABenchToB: a genome assembly benchmark tuned on bacteria and benchtop sequencers.
Jünemann S, Prior K, Albersmeier A, Albaum S, Kalinowski J, Goesmann A, Stoye J, Harmsen D., PLoS One 9(9), 2014
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Jünemann S, Prior K, Albersmeier A, Albaum S, Kalinowski J, Goesmann A, Stoye J, Harmsen D., PLoS One 9(9), 2014
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Application of ion torrent sequencing to the assessment of the effect of alkali ballast water treatment on microbial community diversity.
Fujimoto M, Moyerbrailean GA, Noman S, Gizicki JP, Ram ML, Green PA, Ram JL., PLoS One 9(9), 2014
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An evaluation of alternative methods for constructing phylogenies from whole genome sequence data: a case study with Salmonella.
Pettengill JB, Luo Y, Davis S, Chen Y, Gonzalez-Escalona N, Ottesen A, Rand H, Allard MW, Strain E., PeerJ 2(), 2014
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Reply to Updating benchtop sequencing performance comparison.
Pallen MJ., Nat Biotechnol 31(4), 2013
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RNA-Seq facilitates a new perspective on signal transduction and gene regulation in important plant pathogens.
Vorhölter FJ., Mol Microbiol 88(6), 2013
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Vorhölter FJ., Mol Microbiol 88(6), 2013
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New generation sequencing in pathogen discovery and microbial surveillance.
Calistri A, Salata C, Parolin C, Palù G., Expert Rev Anti Infect Ther 11(9), 2013
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MLST revisited: the gene-by-gene approach to bacterial genomics.
Maiden MC, Jansen van Rensburg MJ, Bray JE, Earle SG, Ford SA, Jolley KA, McCarthy ND., Nat Rev Microbiol 11(10), 2013
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L_RNA_scaffolder: scaffolding genomes with transcripts.
Xue W, Li JT, Zhu YP, Hou GY, Kong XF, Kuang YY, Sun XW., BMC Genomics 14(), 2013
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High-throughput DNA sequencing errors are reduced by orders of magnitude using circle sequencing.
Lou DI, Hussmann JA, McBee RM, Acevedo A, Andino R, Press WH, Sawyer SL., Proc Natl Acad Sci U S A 110(49), 2013
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