Bulk, single-cell, and long-read RNA sequencing solutions.
From cost-effective bulk profiling to high-resolution single-cell and long-read analysis, we deliver comprehensive transcriptomic solutions. Our proprietary SmartComplete and Smart-3SEQ protocols, combined with industry-leading platforms (10X Genomics, SeekGene, and the new Illumina 3' scRNA), allow us to uncover transcriptional heterogeneity, novel isoforms, and RNA modifications, even in challenging, low-input, or fragmented samples like nasal swabs and FFPE tissues.
Specialized protocols for difficult inputs, including fragmented RNA, low-biomass samples (nasal swabs), and single-cell suspensions.
Choice of SmartComplete (full-length total RNA), Smart-3SEQ (cost-effective 3' profiling), 10X Genomics, SeekGene, and the Illumina PIPseq solution for optimized single-cell resolution.
Oxford Nanopore Technologies for full-length transcript reconstruction, alternative splicing detection, and direct RNA modification profiling.
Custom pipelines for differential expression, isoform quantification, and cell-type deconvolution.
Identifying transcriptional signatures in blood, tissue, or liquid biopsies for diagnostic development.
Deconvoluting complex cell populations and immune infiltration in cancer samples.
Detecting alternative splicing events and RNA modifications using long-read sequencing.
Profiling degraded or low-quality RNA samples (e.g., nasal swabs, archived tissues) where standard kits fail.
Our transcriptomics workflow supports flexible entry points — bring tissue or bring RNA.
Not sure your sample qualifies? Contact us to check →
Yes. Our Smart-3SEQ protocol is specifically designed for fragmented or degraded samples, including FFPE tissue and nasal swabs.
We run Illumina (NovaSeq, NextSeq) for short-read and Oxford Nanopore for long-read sequencing. Platform choice depends on your research question.
Tell us about your project and we'll scope a solution for your lab.
