Learn about the specifications and usage instructions of the 100018-USG TELL-Seq Library Sequencing Kit by Universal Sequencing Technology Corporation. Discover the components, library structure, sequencing scheme, and requirements for optimal performance.
Discover the TELL-SeqTM Target Enrichment Kit user guide by Universal Sequencing Technology Corporation. Learn about the specifications, kit contents, genomic DNA input recommendations, and the human exome capture workflow. Ensure optimal results with this essential tool for genomic sequencing applications.
Discover the TELL-Seq™ Target Enrichment User Guide by Universal Sequencing Technology Corporation. Learn about product specifications, genomic DNA requirements, kit contents, and storage recommendations for optimal results. Get insights on using fluorometric-based methods for accurate DNA quantification and enhancing sequencing success.
Discover the TELL-Seq Library Sequencing Kit by Universal Sequencing Technology Corporation. Learn about the specifications, kit contents, and custom sequencing primer requirements. Ensure optimal performance for your research with this innovative product designed for Illumina sequencing systems. Ideal for researchers seeking high-quality sequence data with specific read length requirements.
User guide for the Ion Torrent™ Genexus™ Integrated Sequencer, a next-generation sequencing system by Thermo Fisher Scientific that automates library preparation, template preparation, and sequencing. It covers instrument operation, software usage, and workflow management for research applications.
Explore the automated generation of Twist Bioscience libraries for high-throughput sequencing using HotMPS chemistry on MGI's DNBSEQ platforms. This document details the workflow, experimental results, and performance metrics for DNA and RNA sequencing, highlighting high recall, precision, and reproducibility.
A comprehensive guide for evaluating sequencing run performance and troubleshooting issues with the PacBio Revio system, covering metrics, controls, and common problems.
Comprehensive guide to the Illumina NovaSeq 6000 Sequencing System, covering setup, operation, workflows, maintenance, and troubleshooting for high-throughput genomic research.
A quick start guide for setting up and verifying the PromethION 2 Solo device, including pre-installation checks, device setup, hardware checks, and power-off procedures.
A concise guide to setting up and performing a hardware check on the Oxford Nanopore PromethION 2 Solo sequencing device, including connection, setup, and technical specifications.
Oxford Nanopore Technologies plc announces its interim results for the six months ended 30 June 2025, detailing strong first-half performance, revenue growth ahead of expectations, improved EBITDA, and reaffirmed financial guidance. The report covers operational and strategic achievements, including innovation and partnerships.
This technical note from Element Biosciences compares the AVITI24 System with the AVITI System, highlighting increased sequencing output, improved pass-filter reads, and comparable quality metrics across Whole-Genome Sequencing (WGS), RNA-Seq, scRNA-Seq, and Trinity applications. It details performance data and run conditions.
Official qualification certificate for the Illumina CN NextSeq™ 550Dx Sequencing Reaction Universal Reagent Kit (Lot A185054). This document confirms the product meets technical performance requirements, detailing kit contents, testing conditions, and key results like sequencing throughput and base call quality.
A comprehensive protocol for Ligation Sequencing DNA V14 (SQK-LSK114) by Oxford Nanopore Technologies, detailing steps for DNA repair, end-prep, adapter ligation, library preparation, and flow cell setup for MinION and GridION devices.
Detailed protocol for preparing genomic DNA (gDNA) for sequencing using the Oxford Nanopore Technologies Native Barcoding Kit 24 V14 (SQK-NBD114.24). Covers DNA repair, end-prep, ligation, clean-up, and flow cell preparation steps.
An overview of the Oxford Nanopore Technologies Rapid WGS workflow for fast, end-to-end identification of pathogenic variants and methylation from blood samples using the PromethION 24. This PCR-free nanopore sequencing approach enables rapid turnaround times, comprehensive variant calling (SNVs, SVs, repeat expansions), and epigenetic analysis from a single dataset.