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Flongle adapter

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Mô tả

Bộ chuyển đổi dành cho MinION dành cho các thử nghiệm hoặc thử nghiệm nhỏ hơn. Flongle được thiết kế để trở thành hệ thống giải trình tự nhanh nhất, dễ tiếp cận nhất và tiết kiệm chi phí nhất cho các thử nghiệm và thử nghiệm nhỏ hơn hoặc được thực hiện thường xuyên hơn.

https://nanoporetech.com/products/sequence/flongle

An adapter for MinION for smaller tests or experiments. Flongle is designed to be the quickest, most accessible and cost-efficient sequencing system for smaller or more frequently performed tests and experiments.

https://nanoporetech.com/products/sequence/flongle

 

Publications:

mRNA vaccine quality analysis using RNA sequencing

https://www.nature.com/articles/s41467-023-41354-y

Biofoundry-scale DNA assembly validation using cost-effective high-throughput long read sequencing

https://www.biorxiv.org/content/10.1101/2023.09.19.558498v1

Haplotyping using long-range PCR and nanopore sequencing of phase variants; lessons learned from the ABCA4 locus

https://www.sciencedirect.com/science/article/pii/S0023683723001034

Towards real-time and affordable strain-level metagenomics-based foodborne outbreak investigations using Oxford Nanopore sequencing technologies

https://www.frontiersin.org/articles/10.3389/fmicb.2021.738284/full

Improving the Diagnosis of Bacterial Infections: Evaluation of 16S rRNA Nanopore Metagenomics in Culture-Negative Samples

https://www.frontiersin.org/articles/10.3389/fmicb.2022.943441/full

Real-time molecular classification of leukemias

https://www.medrxiv.org/content/10.1101/2022.06.22.22276550v1

Transcriptome dataset of six human pathogen RNA viruses generated by nanopore sequencing

https://www.sciencedirect.com/science/article/pii/S2352340922005832?via%3Dihub=

Nanopore sequencing for N1-methylpseudouridine in RNA reveals sequence-dependent discrimination of the modified nucleotide triphosphate during transcription

https://www.biorxiv.org/content/10.1101/2022.06.03.494690v1.full

Long-read sequencing to resolve the parent of origin of a de novo pathogenic UBE3A variant

https://jmg.bmj.com/content/59/11/1082.full

Circuit-seq: Circular reconstruction of cut in vitro transposed plasmids using Nanopore sequencing

https://www.biorxiv.org/content/10.1101/2022.01.25.477550v1

Long-read nanopore DNA sequencing can resolve complex intragenic duplication/deletion variants, providing information to enable preimplantation genetic diagnosis

https://obgyn.onlinelibrary.wiley.com/doi/10.1002/pd.6089

Accurate detection of circulating tumor DNA using nanopore consensus sequencing

https://www.nature.com/articles/s41525-021-00272-y

Genome-Guided Discovery of Natural Products through Multiplexed Low-Coverage Whole-Genome Sequencing of Soil Actinomycetes on Oxford Nanopore Flongle

https://journals.asm.org/doi/10.1128/msystems.01020-21

Adaptive nanopore sequencing on miniature flow cell detects extensive antimicrobial resistence

https://www.biorxiv.org/content/10.1101/2021.08.29.458107v1

A Rapid and Cost-Effective Identification of Invertebrate Pests at the Borders Using MinION Sequencing of DNA Barcodes

https://www.mdpi.com/2073-4425/12/8/1138

Development and evaluation of a nanopore 16S rRNA gene sequencing service for same day targeted treatment of bacterial respiratory infection in the intensive care unit

https://www.journalofinfection.com/article/S0163-4453(21)00308-X/fulltext

Long-read nanopore sequencing enables accurate confirmation of a recurrent PMS2 insertion–deletion variant located in a region of complex genomic architecture

https://www.sciencedirect.com/science/article/abs/pii/S2210776221001186?dgcid=author

Rapid genotyping of tilapia lake virus (TiLV) using Nanopore sequencing

https://onlinelibrary.wiley.com/doi/10.1111/jfd.13467?af=R