High-throughput sequencing for transcriptomics, genomics, and beyond
Our Next-Generation Sequencing (NGS) services provide the throughput and depth needed for transcriptomics, whole genome analysis, and comprehensive variant detection. We offer both Illumina and NanoPore platforms, plus combined approaches for the most accurate results.
NGS projects require careful experimental design to ensure you get the data quality and coverage needed for your specific research questions. That's why all our NGS services begin with a consultation—we'll work with you to design the optimal approach for your project.
Whether you're studying gene expression changes, characterizing a genome, or detecting structural variants, our team has the expertise to guide you from experimental design through data delivery.
Choose the platform and approach that fits your research
High-accuracy short-read sequencing for gene expression analysis. Industry-standard platform for transcriptomics with excellent quantification and sensitivity.
Long-read sequencing for applications where read length matters. Ideal for structural variant detection, full-length transcript analysis, and de novo assembly.
Combine the accuracy of short reads with the structural resolution of long reads. The gold standard for comprehensive variant calling and genome characterization.
We'll discuss your research goals, recommend the optimal approach, and provide a detailed quote tailored to your project.
Request ConsultationNGS enables discoveries across many fields
Understand drug mechanisms, identify biomarkers, and characterize cellular responses through comprehensive transcriptome profiling.
Detect mutations, characterize tumor heterogeneity, and identify therapeutic targets with deep sequencing approaches.
Identify disease-causing variants, characterize rare diseases, and support diagnostic development with clinical-grade sequencing.
Characterize microbial communities, assemble novel genomes, and study pathogen evolution with long and short-read approaches.
Our team will help you design the optimal NGS approach