Find kits, reagents, and accessories compatible with the NextSeq 1000 and NextSeq 2000 Systems.
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Targeted panel for investigating 203 genes associated with cancer in children and young adults.
Targeted DNA and RNA research panel investigating variants across 161 genes associated with a range of cancer types.
Targeted custom research panels optimized for sequencing specific targets or genomic content of interest.
A customizable targeted panel for detecting fusion genes and measuring gene expression that can include up to 1200 targets of interest.
Targeted, custom RNA research panels optimized for sequencing up to 1200 genomic targets of interest.
Targeted RNA research panel to investigate T cell diversity and clonal expansion by sequencing T cell receptor beta chain rearrangements.
Targeted RNA expression panel investigating 395 genes involved in tumor-immune system interactions.
Rapidly prepare amplicon libraries for Illumina sequencers using AmpliSeq for Illumina library preparation and index adapters.
Tailor panel designs for human disease research efficiently and conveniently by selecting from a catalog of over 5,000 pretested genes.
FFPE-compatible panel for measuring T cell diversity and clonal expansion in tumor samples by sequencing T cell receptor beta chain rearrangements.
Targeted panel that measures expression levels of >20,000 human RefSeq genes.
Manage runs, analyze, store, and share sequencing data in BaseSpace Sequence Hub. Find applications, subscription options, and documentation.
This low- to mid-throughput NGS assay enables labs of any size to identify and track the emergence and prevalence of novel SARS-CoV-2 variants.
This high-throughput NGS assay enables labs to detect SARS-CoV-2 mutations to identify and track the emergence and prevalence of novel variants.
A highly customizable laboratory information management system that allows genomics labs to track samples and manage workflows efficiently and securely.
An interactive omics knowledge base that analyzes private omics data with highly curated public data to help researchers put their data into biological context.
Reagent used to dilute denatured libraries and the PhiX control library prior to sequencing.
High-throughput next-generation sequencing test detects SARS-CoV-2 in patients suspected of COVID-19 and enables virus genome analysis in research use.
A fast, flexible, and scalable cfDNA library preparation kit for highly sensitive mutation detection
A study design tool that combines private data with public data sets for rapidly building and exploring cohorts.
Whole-exome sequencing is used to investigate protein-coding regions of the genome to uncover genetic influences on disease and population health.
With single-cell RNA-Seq, you can study cellular differences often masked by bulk sampling. Explore high- and low-throughput single-cell sequencing methods.
Small genome sequencing provides comprehensive analysis of bacterial, viral, and other microbial genomes for epidemiology and disease studies.