Exome capture-based RNA sequencing is equipped with UMI correction to improve accuracy and adopts a strand-specific library approach to enhance gene expression quantification with the coverage of protein-coding genes.
Product Introduction
Powered by Hybrid-Capture NGS
Uncovering genomic expression patterns and calling fusion and splicing variants. Compatible with low-quality and low-quantity samples. Low RNA input requirement: 20-80 ng.
Outstanding Performance
Strand-specific libraries improve accuracy.
UMI-aided correction of amplification bias. Under 200M reads calling, LoD for fusion and splicing variants is as low as 29 copies/ng.
Broad Sample Compatibility
Supports FFPE and fresh frozen tissue with DNA/RNA co-extraction to maximize genomic insights from limited input. Also compatible with bone marrow, PBMC/WBC, whole blood lysates, and cell lines.
Versatile Integration for Multi-Omics Applications
Seamlessly integrates with DNA sequencing for comprehensive genomic profiling.
Compatible with methylation sequencing to enable multi-omics analysis.
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