Generate complete genome assemblies using long nanopore sequencing reads. Resolve structural variants, repeats, phasing, and base modifications.
Oxford Nanopore sequencing Legacy short-read sequencing Streamlined, automatable workflows Laborious workflows Prepare samplesin as little as 10 minutes, including multiplexing Use end-to-endwhole-genome,metagenomic,targeted(including 16S barcoding),direct RNA and cDNAsequencing workflows ...
Biofoundry-scale DNA assembly validation using cost-effective high-throughput long read sequencing publication2023年9月26日 Nanopore sequencing-based microbiome profiling of the water recovery system onboard the International Space Station poster2023年12月12日 ...
Nanopore sequencing is fully scalable Nanopore sequencing is the only sequencing technology to enable real-time analysis in fully scalable formats. From the pocket-sized MinION to the high-throughput, population-scale PromethION — scale nanopore sequencing to suit any exp...
Oxford Nanopore长读测序技术(Oxford Nanopore Long-Read Sequencing)是一种先进的DNA测序方法,通过利用纳米孔技术实现对DNA分子的高效测序。本文将从技术原理、应用优势以及发展前景等方面对Oxford Nanopore长读测序方法进行详细介绍。 一、 技术原理 Oxford Nanopore长读测序技术是利用纳米孔中的离子传导来测序DNA分子。
publication4 September 2023 Biofoundry-scale DNA assembly validation using cost-effective high-throughput long read sequencingpublication26 September 2023 Oxford nanopore long-read sequencing enables the generation of complete bacterial and plasmid genomes without short-read sequencingpublication1 June 2023...
不同于前两代测序技术,第三代纳米孔测序技术无需PCR扩增,利用纳米孔特殊结构实现单条DNA/RNA分子的实时测序,从而克服了第二代测序技术(NGS)中存在的PCR扩增误差、测序读长短、DNA/RNA甲基化修饰的问题,并广泛应用于基因组测序、突变鉴定等多个研究领域。 01 【产品简介】 Oxford Nanopore Sequencing第三代测序系统...
Whether you are studying the human genome, investigating the microbiome, or exploring the diversity of life on earth, Oxford Nanopore library preparation solutions offer a flexible, cost-effective, and streamlined way to generate high-quality sequencing
Oxford Nanopore sequencing Legacy short-read sequencing Accessible and affordable sequencing Constrained to centralised labs Sequence on demand with flexible end-to-end workflows that suit your throughput needs Sequence at sample source, even in the most extreme or remote environments, with the portableMi...
据了解,这种方法基于Oxford Nanopore公司MinION测序仪和贝叶斯算法,将通过测序发现的随机突变与已知基因组数据库进行比较,可在大约3分钟的测序过程中利用60到300个随机SNP识别出人类DNA,几乎实现了实时的DNA鉴定。相关研究于近日发表于开放获取期刊eLife,论文题为“Rapid re-identification of human samples using portable ...