NEB Scientific Posters
Your search returned 67 results.
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Primer-monitor.neb.com – streaming detection and notification of new SARS-CoV-2 variants
Nucleic acid diagnostic tests for SARS-CoV-2, whether based on RT-qPCR, RT-LAMP, RPA, or other amplification technology, all depend on primers. While the SARS-CoV-2 genome seems to be less variable than some other retroviral genomes, variants with potential effects on amplification efficiency have arisen and become prevalent in local areas. We developed a streaming analysis method to identify variants that may affect specific primers and a website to allow interested users to register primer loci.
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Incorporation of Unique Molecular Identifiers (UMIs) into Unique Dual Indexing (UDI) of samples improves the accuracy of quantitative Next Generation Sequencing
The use of Unique Molecular Identifiers (UMIs) has become increasingly popular, offering a multitude of advantages, especially when paired with unique dual indexing (UDI). By incorporating UMIs into UDI adaptors, we have assessed their effect on the accuracy of quantitative sequencing assays. We demonstrate that the sensitivity of variant detection is improved with UMI consensus calling.
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Improving multiplex targeted amplicon sequencing of SARS-CoV-2 on Illumina platforms
The impact of the novel coronavirus SARS-CoV-2 on the global community has produced a critical need to develop reliable and accurate protocols for sequencing emergent pathogens. Here, we present refined protocols and reagents for the sequencing of SARS-CoV-2 on Illumina sequencing platforms with protocols based on the ARTIC consortium methods.
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Improving transcriptome analysis by incorporating Unique Molecular Identifiers in RNA-sequencing libraries
RNA sequencing is a powerful tool for the study of gene regulation and function. Applications of RNA-seq have expanded to include low-RNA input library prep methods. In this study, we show that the incorporation of UMIs into RNA-seq analysis allows for a more accurate calculation of transcript abundance.
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A Novel Method for High Molecular Weight (HMW) DNA Extraction
The need for very high molecular weight (HMW) DNA is growing quickly as long read sequencing and other emerging long read technologies become increasingly popular. However, the extraction of HMW DNA has been a bottleneck for these applications, and rapid, efficient and affordable HMW DNA extraction solutions are highly sought after. Here, we present a novel approach to HMW DNA extraction that utilizes large glass beads and optimized buffer chemistry, resulting in a simple workflow that enables researchers to quickly purify high quality HMW DNA from cells, blood, tissue and bacteria using two dedicated Monarch Kits. Purified DNA ranges from 50 kb to several megabases and size can be tuned by varying the speed at which samples are agitated during lysis. The use of glass beads enables easy handling, extremely efficient elution, high recovery, and easy dissolving of the isolated HMW DNA.
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Increasing Sensitivity of Transcriptome Profiling in Prokaryotic and Eukaryotic Samples by Depleting Abundant RNAs
RNA-Seq is a widely used technology with a broad range of applications, including differential expression analysis and alternative splice forms identification, in normal and disease contexts as well as in developmental studies. The technology has been pushed to extremes of very low and degraded samples but still battles with the challenge of having a large dynamic range of transcript expression. Highly expressed transcripts with minimal biological interest can dominate readouts, masking detection of more informative low-abundance transcripts. Here, we present an improved method to enrich for RNAs of interest by eliminating abundant, typically unwanted, RNAs.
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Increasing Power to Detect Low-Frequency Variants Using Dual-Unique Molecular Indices
The use of Unique Molecular Identifiers (UMIs) has become increasingly popular – offering a multitude of advantages – particularly when paired with Unique Dual Indices (UDI). Two major factors affecting sequencing accuracy are 1) duplication, arising from PCR amplification of library molecules, and 2) errors introduced during library preparation and sequencing on the flow cell. UMIs, when incorporated into library preparation, can account for and mitigate the impacts of both of these factors. UMIs improved the accuracy of low-frequency variant detection by 25-200%.
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A Customizable Approach for Selective Removal of Abundant RNAs Enhances the Sensitivity of Transcript Detection Across Species
We developed a user-friendly web tool to enable custom depletion of any RNAs of interest. We used this web tool and depletion method to remove rRNA from total RNA of various species, including the mosquito Aedes aegypti as well as archaea Thermococcus kodakarensis and Pyrococcus furiosus. Additionally, we used this approach to target coding RNAs in human total RNA, and supplemented an existing anti-rRNA probe set for depletion of both rRNA and the selected coding RNAs. Using strand-specific RNA sequencing we measured depletion efficiency and transcript expression. We achieved high depletion efficiency (up to 99%) for all targeted RNAs across species, while maintaining transcript abundance of non-targeted RNA. This translated into an enrichment of RNAs of interest and an increased depth of sequencing coverage.
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Induro™, a Novel Reverse Transcriptase for Nanopore Direct RNA Sequencing with Significantly Improved RNA 5′ Coverage
Induro Reverse Transcriptase is an intron-encoded RT with superior performance in the cDNA synthesis reaction. Longer read lengths, higher percentage of full-length genes and transcripts, and improved 5′ coverage can be achieved with Induro RT without increasing error rates or decreasing mapping rates, enabling direct RNA sequencing on the Oxford Nanopore Technologies® platform.
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A highly multiplexed target enrichment approach for sample identification and tracking using the NEBNext Direct Genotyping Solution
Next-generation sequencing is increasingly being adopted for genetic screening and clinical diagnostics.
To prevent false reporting of results, it is imperative that patient samples are tracked throughout sample processing and data analysis. A reliable method to track sample identity throughout a workflow is to monitor single nucleotide polymorphisms (SNPs) that are highly discriminatory across individuals. In order to incorporate a routine sample tracking method into diagnostic workflows, the method should be reliable, high-throughput, and cost-effective. The NEBNext Direct® Genotyping Solution offers a convenient and reliable method to ensure that data integrity is maintained in a diagnostic workflow.
