Our powerful RNA-seq panels and kits can help you unravel the intricacies of the genome and transcriptome in biomarker research, gene expression studies, viral epidemiology and disease surveillance.
PCR bias and sequencing artifacts can jeopardize the sensitivity of your data, but we’ve included single primer extension (SPE) and unique molecular index (UMI) technologies to increase the precision, accuracy and coverage of your quantification studies.
These products support a wide range of RNA sequencing applications, including whole transcriptome analysis, targeted gene expression profiling, sequencing of single-cell or ultralow input samples, immune repertoire screening, RNA fusion detection and SNV analysis. Plus, our optimized workflows and integrated data analysis pipeline help you accumulate insights faster and easier than ever.
Comprehensive oncology profiling combining gene fusion detection, gene expression analysis and single nucleotide variant (SNV) calling in just one assay
Comprehensive oncology profiling combining gene fusion detection, gene expression analysis and single nucleotide variant (SNV) calling in just one assay
Applying digital RNA sequencing to scan for known and novel fusion genes
Applying digital RNA sequencing to scan for known and novel fusion genes
For ultraplex (UPX) gene expression analysis using 3' RNA-seq from single cells and low-input samples
For preparation of stranded whole transcriptome RNA-seq libraries for NGS applications on Illumina instruments, including optional purification of poly A+ RNA from total RNA
For high-throughput 3' transcriptome analysis from up to 10 ng of purified RNA, cell lysates and single cells using next-generation sequencing
A single day sample to sequencing workflow for simultaneous enrichment and profiling of DNA variants, RNA fusions and gene expression levels from one sample input, as low as 10 ng
A single day sample to sequencing workflow for simultaneous enrichment and profiling of DNA variants, RNA fusions and gene expression levels from one sample input, as low as 10 ng
The only one-day, low-input sample to sequencing workflow for simultaneous and comprehensive genomic profiling of DNA variants, RNA fusions and assessing TMB/MSI in solid tumors and heme malignancies
For rapid removal of unwanted RNAs during RNA-seq library preparation
For targeted whole genome library preparation of SARS-CoV-2 for genomic surveillance and variant detection
For fast, targeted whole genome library preparation of SARS-CoV-2 for genomic surveillance and variant detection
For the culture-free Whole Genome Enrichment of Mycobacterium tuberculosis
For high-quality targeted viral and bacterial sequencing using hybrid capture