Choose the sequencing service that fits your research. High-throughput, high-accuracy, across all major platforms including Illumina, PacBio, Oxford Nanopore, and more.
Full-length sequencing of PCR products and plasmids using long-read technology, no assembly artifacts, complete coverage in one read.
Whole Genome Sequencing at high coverage, from variant discovery and structural analysis to de-novo assembly.
Comprehensive transcriptome profiling for gene expression analysis, splice variant discovery, and novel transcript detection.
For labs with in-house library prep. Submit your libraries and receive high-quality sequencing data, fast and at scale.
Cost-effective whole exome sequencing covering all protein-coding regions, ideal for variant discovery and clinical research.
Ultra-deep targeted sequencing of specific genomic loci using custom or validated amplicon panels, high sensitivity at low cost.
Comprehensive microbial community profiling, from 16S amplicon surveys to shotgun metagenomics for full functional analysis.
Profile the active microbial community, sequence the expressed RNA to reveal gene expression, functional activity, and which microbes are alive and working.
Don't see your project among the services above? Tell us what you need — any sequencing, analysis, or combination — and our scientific team will get back to you with a tailored quote.
