nebnext companion module for oxford nanopore technologies ligation sequencing (New England Biolabs)
97
Structured Review
New England Biolabs
nebnext companion module for oxford nanopore technologies ligation sequencing
Nebnext Companion Module For Oxford Nanopore Technologies Ligation Sequencing, supplied by New England Biolabs, used in various techniques. Bioz Stars score: 97/100, based on 32 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/nebnext+companion+module/NEBNext+Companion+Module+for+Oxford/pmc13125923-18-0-0
Average 97 stars, based on 32 article reviews
Nebnext Companion Module For Oxford Nanopore Technologies Ligation Sequencing, supplied by New England Biolabs, used in various techniques. Bioz Stars score: 97/100, based on 32 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/nebnext+companion+module/NEBNext+Companion+Module+for+Oxford/pmc13125923-18-0-0
Average 97 stars, based on 32 article reviews
nebnext companion module for oxford nanopore technologies ligation sequencing - by Bioz Stars,
2026-09
97/100 stars
Images
Related Articles
Sequencing:Article Title: A Bioinformatic Pipeline for Consensus Taxonomic Classification of Long-Read Amplicons Article Snippet: PCR products were pooled into libraries at roughly equal concentrations, as estimated from gel band intensities, and purified using a Monarch PCR & DNA cleanup kit (NEB). .. ONT sequencing was performed at SeqCenter (Pittsburg, PA), with library preparation using the PCR-free ONT Ligation Sequencing Kit (SQK-NBD114.24) with Article Title: Cranberry juice potentiates sensitivity of uropathogenic Escherichia coli (UPEC) strains to fosfomycin and decreases occurrence of spontaneous resistance. Article Snippet: .. For long-read sequencing, libraries were prepared without PCR amplification using the Oxford Nanopore Technologies (ONT) Native Barcoding Kit (SQK-NBD114.24) in combination with the Article Title: Psychrobacillus syltrankelensis sp. nov., a new species isolated from soil in the North Caucasus, Russia. Article Snippet: Genomic DNA for Oxford Nanopore sequencing was isolated using the MagBeads FastDNA Kit for Microbiome (MP Biomedicals, Santa Ana, CA, USA) according to the manufacturer’s instructions. .. Libraries were prepared following the manufacturer’s protocol with the Native Barcoding Kit 24 V14 (Oxford Nanopore Technologies Ltd, Oxford, UK), the Article Title: Whole-Genome Long-Read Sequencing for Rapid Comprehensive Molecular Diagnostics of Brain Tumors Article Snippet: Genomic DNA was extracted from fresh or frozen biopsies using the DNeasy Blood & Tissue kit (Qiagen). .. Sequencing libraries were prepared with the Article Title: Long-Read Haplotype Phasing Resolves Allelic Configuration as a Missing Layer of Precision Oncology Article Snippet: Samples with a high proportion of short DNA fragments were further processed using the BluePippin High-Pass DNA Size Selection System (Sage Science) to enrich for fragments greater than 5 kb, suitable for nanopore sequencing. .. Sequencing libraries were prepared using the Ligation Sequencing Kit V14 (SQK-LSK114; Oxford Nanopore Technologies) in combination with the Article Title: Unraveling the potential of short and long read sequencing for human genome profiling Article Snippet: .. We prepared the ONT library from 1.0 μg gDNA input (with no short read eliminator treatment), sheared using Megaruptor 3 (Diagenode) at speed 33 in a volume of 100 μL, using Ligation Sequencing kit V14 (ONT) and Article Title: Genome Dynamics and Chromosome Structural Variations in Histoplasma ohiense, a fungal pathogen of humans. Article Snippet: .. 116 117 Nanopore sample libraries were prepared using the PCR-free Oxford Nanopore Technologies (ONT) Ligation 118 Sequencing Kit (SQK-NBD114.24) with the Polymerase Chain Reaction:Article Title: A Bioinformatic Pipeline for Consensus Taxonomic Classification of Long-Read Amplicons Article Snippet: PCR products were pooled into libraries at roughly equal concentrations, as estimated from gel band intensities, and purified using a Monarch PCR & DNA cleanup kit (NEB). .. ONT sequencing was performed at SeqCenter (Pittsburg, PA), with library preparation using the PCR-free ONT Ligation Sequencing Kit (SQK-NBD114.24) with Article Title: Cranberry juice potentiates sensitivity of uropathogenic Escherichia coli (UPEC) strains to fosfomycin and decreases occurrence of spontaneous resistance. Article Snippet: .. For long-read sequencing, libraries were prepared without PCR amplification using the Oxford Nanopore Technologies (ONT) Native Barcoding Kit (SQK-NBD114.24) in combination with the Article Title: Genome Dynamics and Chromosome Structural Variations in Histoplasma ohiense, a fungal pathogen of humans. Article Snippet: .. 116 117 Nanopore sample libraries were prepared using the PCR-free Oxford Nanopore Technologies (ONT) Ligation 118 Sequencing Kit (SQK-NBD114.24) with the Ligation:Article Title: A Bioinformatic Pipeline for Consensus Taxonomic Classification of Long-Read Amplicons Article Snippet: PCR products were pooled into libraries at roughly equal concentrations, as estimated from gel band intensities, and purified using a Monarch PCR & DNA cleanup kit (NEB). .. ONT sequencing was performed at SeqCenter (Pittsburg, PA), with library preparation using the PCR-free ONT Ligation Sequencing Kit (SQK-NBD114.24) with Article Title: Psychrobacillus syltrankelensis sp. nov., a new species isolated from soil in the North Caucasus, Russia. Article Snippet: Genomic DNA for Oxford Nanopore sequencing was isolated using the MagBeads FastDNA Kit for Microbiome (MP Biomedicals, Santa Ana, CA, USA) according to the manufacturer’s instructions. .. Libraries were prepared following the manufacturer’s protocol with the Native Barcoding Kit 24 V14 (Oxford Nanopore Technologies Ltd, Oxford, UK), the Article Title: Whole-Genome Long-Read Sequencing for Rapid Comprehensive Molecular Diagnostics of Brain Tumors Article Snippet: Genomic DNA was extracted from fresh or frozen biopsies using the DNeasy Blood & Tissue kit (Qiagen). .. Sequencing libraries were prepared with the Article Title: Long-Read Haplotype Phasing Resolves Allelic Configuration as a Missing Layer of Precision Oncology Article Snippet: Samples with a high proportion of short DNA fragments were further processed using the BluePippin High-Pass DNA Size Selection System (Sage Science) to enrich for fragments greater than 5 kb, suitable for nanopore sequencing. .. Sequencing libraries were prepared using the Ligation Sequencing Kit V14 (SQK-LSK114; Oxford Nanopore Technologies) in combination with the Article Title: Unraveling the potential of short and long read sequencing for human genome profiling Article Snippet: .. We prepared the ONT library from 1.0 μg gDNA input (with no short read eliminator treatment), sheared using Megaruptor 3 (Diagenode) at speed 33 in a volume of 100 μL, using Ligation Sequencing kit V14 (ONT) and Article Title: Genome Dynamics and Chromosome Structural Variations in Histoplasma ohiense, a fungal pathogen of humans. Article Snippet: .. 116 117 Nanopore sample libraries were prepared using the PCR-free Oxford Nanopore Technologies (ONT) Ligation 118 Sequencing Kit (SQK-NBD114.24) with the Sampling:Article Title: A Bioinformatic Pipeline for Consensus Taxonomic Classification of Long-Read Amplicons Article Snippet: PCR products were pooled into libraries at roughly equal concentrations, as estimated from gel band intensities, and purified using a Monarch PCR & DNA cleanup kit (NEB). .. ONT sequencing was performed at SeqCenter (Pittsburg, PA), with library preparation using the PCR-free ONT Ligation Sequencing Kit (SQK-NBD114.24) with Amplification:Article Title: Cranberry juice potentiates sensitivity of uropathogenic Escherichia coli (UPEC) strains to fosfomycin and decreases occurrence of spontaneous resistance. Article Snippet: .. For long-read sequencing, libraries were prepared without PCR amplification using the Oxford Nanopore Technologies (ONT) Native Barcoding Kit (SQK-NBD114.24) in combination with the |