Find kits, reagents, and accessories compatible with the MiniSeq System.
55 Results
Targeted research panel investigating somatic and germline variants in BRCA1 and BRCA2.
Targeted research panel investigating hotspot regions of 50 genes with known associations to cancer.
Targeted panel for investigating 203 genes associated with cancer in children and young adults.
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 DNA and RNA research panel investigating 52 genes with known relevance to solid tumors.
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.
Targeted panel to investigate 40 DNA genes, 29 RNA fusion driver genes, and 5 gene expression levels associated with myeloid cancers.
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.
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 and data search engine that puts private data into biological context with highly curated public omics data.
Reagent used to dilute denatured libraries and the PhiX control library prior to sequencing.
Four 96-sample unique dual index plates used with Illumina library prep for multiplexing up to 384 samples. Plates are desalted, not HPLC purified.
With targeted sequencing or resequencing, a subset of genes or a genomic region of interest is isolated and sequenced, which can conserve lab resources.
The MiniSeq System delivers simple, accessible benchtop sequencing for targeted DNA and RNA applications.
NGS-based microbial sequencing methods include shotgun metagenomics, 16S rRNA sequencing, whole-genome and de novo sequencing, and transcriptomics.