
Precision immunotherapies using turmor-specific HLA ligands
Learn how researchers at Immatics are using the MiniSeq System to help identify novel immunotherapy targets.
Accessible cross-method flexibility
Transition easily between sequencing methods for DNA and RNA applications
Targeted DNA sequencing allows researchers to focus on a select set of genes or relevant gene regions using fixed panels of expert-selected content or custom, user-defined gene panels. By focusing the power of next-generation sequencing (NGS), targeted sequencing enables cost-effective and systematic variant detection with high accuracy and reproducibility.
A highly multiplexed polymerase chain reaction (PCR)–based workflow for use with targets ranging from a few to hundreds of genes in a single run.
DesignStudio Assay Design Tool
A web-based assay design tool to help researchers design and order custom sequencing probes or create custom genotyping array assays.
Ready-to-use reagent kits include the reagent cartridge, flow cell, and hybridization buffer for use with the MiniSeq System.
This software provides a user-friendly integrated solution for creating sequencing runs, monitoring run status, and analyzing data.
The Illumina genomics cloud-computing environment for NGS data analysis and management.
Our variant annotation and analysis software tools can help researchers extract and report biological insights from large volumes of genomic data.
Resource spotlight
Learn how the MiniSeq System coupled with other Illumina solutions enabled Phosphorus to perform genomic analysis onsite at an accessible price point.
Sequence the 16S ribosomal RNA (rRNA) gene with a culture-free method to identify and compare bacteria from complex, difficult-to-study microbiomes or environments.
Enable fast, accurate characterization of novel genomes with no reference sequence available for any species.
Discover novel plant and animal SNPs and perform genotyping studies with a low-cost genetic screening method.
Assess genes with known or suspected associations with an increased hereditary risk of cancer.
Leverage NGS to detect and characterize viruses, bacteria, fungi, and parasites for research applications.
Isolate and sequence small RNA species, such as microRNA, to study the role of noncoding RNA in gene silencing and posttranscriptional regulation.
Select and sequence specific genes or genomic regions of interest using predesigned or custom designed panels for gene profiling studies.
See what’s possible with the MiniSeq System
Learn how researchers at Immatics are using the MiniSeq System to help identify novel immunotherapy targets.