flow cell (Oxford Nanopore)
96
Structured Review
Oxford Nanopore
flow cell
Flow Cell, supplied by Oxford Nanopore, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/flo-flg114/bio_rxiv__2025__01__02__631154-146-14-9
Average 96 stars, based on 1 article reviews
Flow Cell, supplied by Oxford Nanopore, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/flo-flg114/bio_rxiv__2025__01__02__631154-146-14-9
Average 96 stars, based on 1 article reviews
flow cell - by Bioz Stars,
2026-09
96/100 stars
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Related Articles
Sequencing:Article Title: Can α-Mangostin and Photodynamic Therapy Support Ciprofloxacin in the Inactivation of Uropathogenic Escherichia coli and Staphylococcus aureus Strains? Article Snippet: Libraries were prepared using the Rapid Barcoding Kit 24 V14 (SQK-RBK114.24, Oxford Nanopore Technologies, Oxford, UK). .. Sequencing was performed on a MinION Mk1B instrument using a Article Title: A novel barcoded nanopore sequencing workflow of high-quality, full-length bacterial 16S amplicons for taxonomic annotation of bacterial isolates and complex microbial communities Article Snippet: .. For the loading of the library, 15 μL sequencing buffer, 10 μL loading beads, and 5 μL of the final library were mixed and loaded onto a Article Title: Synthetic mismatches enable specific CRISPR-Cas12a-based detection of genome-wide SNVs tracked by ARTEMIS. Article Snippet: In brief Cas12a-based SNV detection often yields false positives due to mismatch tolerance.. Kohabir et al. present ARTEMIS, a pipeline pinpointing clinically relevant SNVs within Cas12a seed regions.. By incorporating synthetic mismatches, their method enhances single-nucleotide fidelity in CRISPRbased detection of several cancerassociated variants, includingBRAF, promising precise and cost-effective genetic diagnostics. Article Title: Iron retention coupled with trade-offs in localized symbiotic effects confers tolerance to combined iron deficiency and drought in soybean Article Snippet: Amplicons from each sample were ligated to pooled barcoded reads with the 16S Barcoding Kit 24 V14 (SQK-16S114-24, Oxford Nanopore Technologies, Oxford, UK) for library creation. .. The sequencing was done on a MinION portable sequencer (Oxford Nanopore Technologies) with a Article Title: Draft genome of a human gut-derived Blautia sp. that ameliorates colitis and colitis-associated sociability deficits in mice. Article Snippet: Blautia is a genus of anaerobic, gram-positive bacteria commonly found in mammalian gastrointestinal tracts.. Yet, how variations among different Blautia strains can impact host health is poorly understood.. We present a Blautia sp. genome isolated from human feces whose supplementation to mice can ameliorate colitis severity and associated sociability deficits. Article Title: Hypothesis-based investigation of known AD risk variants reveals the genetic underpinnings of neuropathological lesions observed in Alzheimer’s-type dementia Article Snippet: Library preparation was performed using the ligation sequencing kit LSK110 (Oxford Nanopore Technology) according to the accompanying protocol. .. Sequencing was performed on a Ligation:Article Title: Synthetic mismatches enable specific CRISPR-Cas12a-based detection of genome-wide SNVs tracked by ARTEMIS. Article Snippet: In brief Cas12a-based SNV detection often yields false positives due to mismatch tolerance.. Kohabir et al. present ARTEMIS, a pipeline pinpointing clinically relevant SNVs within Cas12a seed regions.. By incorporating synthetic mismatches, their method enhances single-nucleotide fidelity in CRISPRbased detection of several cancerassociated variants, includingBRAF, promising precise and cost-effective genetic diagnostics. Variant Assay:Article Title: Synthetic mismatches enable specific CRISPR-Cas12a-based detection of genome-wide SNVs tracked by ARTEMIS. Article Snippet: In brief Cas12a-based SNV detection often yields false positives due to mismatch tolerance.. Kohabir et al. present ARTEMIS, a pipeline pinpointing clinically relevant SNVs within Cas12a seed regions.. By incorporating synthetic mismatches, their method enhances single-nucleotide fidelity in CRISPRbased detection of several cancerassociated variants, includingBRAF, promising precise and cost-effective genetic diagnostics. Genome Wide:Article Title: Synthetic mismatches enable specific CRISPR-Cas12a-based detection of genome-wide SNVs tracked by ARTEMIS. Article Snippet: In brief Cas12a-based SNV detection often yields false positives due to mismatch tolerance.. Kohabir et al. present ARTEMIS, a pipeline pinpointing clinically relevant SNVs within Cas12a seed regions.. By incorporating synthetic mismatches, their method enhances single-nucleotide fidelity in CRISPRbased detection of several cancerassociated variants, includingBRAF, promising precise and cost-effective genetic diagnostics. Planar Chromatography:Article Title: Synthetic mismatches enable specific CRISPR-Cas12a-based detection of genome-wide SNVs tracked by ARTEMIS Article Snippet: Nanopore Native Barcoding Kit 24 V14 , Oxford Nanopore Technologies plc. , Cat#SQK-NBD114.24. .. Nanopore flongle flow cell R10.4.1 , |