Use end-to-end whole-genome,metagenomic,targeted(including 16S barcoding),direct RNA and cDNAsequencing workflows Scale andautomateyour workflows to suit your sequencing needs Perform real-time enrichment of single targets or panels without additional wet-lab prep by usingadaptive sampling ...
测序技术的发展是人类对基因研究的转折点,使人类对基因组的研究从“盲人摸象”阶段走向更宽广与更精确的方向。全基因组重测序(Whole Genome Sequencing,WGS)是对已知基因组序列的物种进行不同个体的基因组测序,并在此基础上对个体或群体进行差异性分析。目前此技术已经广泛应用于医学领域,主要应用方向有寻找肿瘤突变位点...
12. Votintseva, A. A. et al. Sameday diagnostic and surveillance data for tuberculosis via whole genome sequencing of direct respiratory samples. J. Clin. Microbiol. JCM.02483-16 (2017). doi:10.1128/JCM.02483-16 13. Schmidt, K...
Workflow: bacterial isolate sequencing To learn more about the protocol in this application note, you can download therapid end-to-end workflow for whole-genome sequencing of bacterial isolatesusing MinION Flow Cells on MinION or GridION sequencing devices and the EPI2ME analysis platform. ...
Whole genome sequencing and assembly of a Caenorhabditis elegans genome with complex genomic rearrangements using the MinION sequencing device 建库信息 (2D) ONT sequencing library(SQK-LSK108),上机4 MinION flowcells(R9.0)48hrs (1D) ONT sequencing library(SQK-RAD001),上机2 MinION flowcells(R9.3)48...
Human anthrax cases necessitate rapid response. We completed Bacillus anthracis nanopore whole-genome sequencing in our high-containment laboratory from a human anthrax isolate hours after receipt. The de novo assembled genome showed no evidence of known antimicrobial resistance genes or introduced plasmid...
Whole-genome sequencing (WGS) is becoming widely used in clinical medicine in diagnostic contexts and to inform treatment choice. Here we evaluate the potential of the Oxford Nanopore Technologies (ONT) MinION long-read sequencer for routine WGS by sequencing the reference sample NA12878 and the ge...
Whole-Genome Sequence analysis of Clinically Isolated Carbapenem ResistantEscherichiacolifrom Iran (IRANCOLI ONT,SRR21721846,SRR21721848)。 #下载 MinION sequencing: IRANCOLI ONT, SRR21721846$ wget-c-t0ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR217/046/SRR21721846/SRR21721846_1.fastq.gz#数据大小521M...
[1] Fujimoto A et al. Whole-genome sequencing with long reads reveals complex structure and origin of structural variation in human genetic variations and somatic mutations in cancer. Genome Medicine, 2021. 作者:胡潇雨,韩婉...
Fujimoto A, Wong JH, Yoshii Y,et al. Whole-genome sequencing with long reads reveals complex structure and origin of structural variation in human genetic variations and somatic mutations in cancer.Genome Med. 2021;13(1...