Results 21 to 30 of about 33,843 (263)

Nanopore Technology and Its Applications in Gene Sequencing

Biosensors, 2021
In recent years, nanopore technology has become increasingly important in the field of life science and biomedical research. By embedding a nano-scale hole in a thin membrane and measuring the electrochemical signal, nanopore technology can be used to ...
Bo Lin, Jianan Hui, Hongju Mao
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Benchmarking methylation-calling tools for Oxford Nanopore Sequencing

, 2021
Benchmarking methylation-calling tools for Oxford Nanopore ...
Yang Liu
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A chromosome-level genome assembly of the redfin culter (Chanodichthys erythropterus)

Scientific Data, 2022
Measurement(s) whole genome sequencing Technology Type(s) Oxford Nanopore Sequencing Sample Characteristic - Organism Chanodichthys ...
Shihu Zhao, Xiufeng Yang, Bo Pang, Lei Zhang, Qi Wang, Shangbin He, Huashan Dou, Honghai Zhang   +7 more
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Oxford Nanopore Technologies sequencing analysis pipeline.

, 2021
Flowchart shows each step taken to generate recombinant sequences from Oxford Nanopore sequencing data. Boxes represent processes in the pipeline, diamonds represent decision points and ovals represent termination points. (TIF)
David J. Evans (208308), Kirsten Bentley (426888), Andrew Woodman (577477), Fadi Ghassan Alnaji (11307931), Siân Jones (6986), Luke Woodford (576538)   +5 more
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Interchromosomal template-switching as a novel molecular mechanism for imprinting perturbations associated with Temple syndrome

Genome Medicine, 2019
Background Intrachromosomal triplications (TRP) can contribute to disease etiology via gene dosage effects, gene disruption, position effects, or fusion gene formation.
Claudia M. B. Carvalho, Zeynep Coban-Akdemir, Hadia Hijazi, Bo Yuan, Matthew Pendleton, Eoghan Harrington, John Beaulaurier, Sissel Juul, Daniel J. Turner, Rupa S. Kanchi, Shalini N. Jhangiani, Donna M. Muzny, Richard A. Gibbs, Baylor-Hopkins Center for Mendelian Genomics, Pawel Stankiewicz, John W. Belmont, Chad A. Shaw, Sau Wai Cheung, Neil A. Hanchard, V. Reid Sutton, Patricia I. Bader, James R. Lupski   +21 more
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An Introduction to Nanopore Sequencing: Past, Present, and Future Considerations

Micromachines, 2023
There has been significant progress made in the field of nanopore biosensor development and sequencing applications, which address previous limitations that restricted widespread nanopore use.
Morgan MacKenzie, Christos Argyropoulos
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Nanopore sequencing technology and its application in plant virus diagnostics

Frontiers in Microbiology, 2022
Plant viruses threaten crop yield and quality; thus, efficient and accurate pathogen diagnostics are critical for crop disease management and control. Recent advances in sequencing technology have revolutionized plant virus research.
Kai Sun, Yi Liu, Xin Zhou, Chuanlin Yin, Pengjun Zhang, Qianqian Yang, Lingfeng Mao, Xuping Shentu, Xiaoping Yu   +8 more
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Nanocall: an open source basecaller for Oxford Nanopore sequencing data [PDF]

, 2017
MotivationThe highly portable Oxford Nanopore MinION sequencer has enabled new applications of genome sequencing directly in the field. However, the MinION currently relies on a cloud computing platform, Metrichor (metrichor.com), for translating locally
Simpson, Jared T, Yao, Delia, David, Matei, Dursi, LJ, Boutros, Paul C   +4 more
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Absence of evidence is not evidence of absence: Nanopore sequencing and complete assembly of the European lobster (Homarus gammarus) mitogenome uncovers the missing nad2 and a new major gene cluster duplication

BMC Genomics, 2019
Background The recently published complete mitogenome of the European lobster (Homarus gammarus) that was generated using long-range PCR exhibits unusual gene composition (missing nad2) and gene rearrangements among decapod crustaceans with strong ...
Han Ming Gan, Frederic Grandjean, Tom L. Jenkins, Christopher Mervyn Austin   +3 more
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Application of Oxford Nanopore sequencing for the study of marine biodiversity

, 2023
reservedIl sequenziamento Oxford Nanopore ha permesso negli ultimi anni di migliorare le analisi metagenomiche, rendendo possibile l’identificazione di informazioni genetiche rilevanti dove le short reads avevano precedentemente fallito. In questo studio
CALLEGARO, ANDREA
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