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NGS panel for clinical exome sequencing, which enables the detection of SNV, InDel and CNV variants in 5500 genes using hybrid capture technology.
NGS panel for whole exome sequencing, which enables the detection of SNV, InDel and CNV variants in 19 425 genes using hybrid capture technology.
Kits for single-cell mRNA library construction for a wide range of applications by combining single-cell whole-transcriptome profiling with target-specific sequencing.
Library preparation kits for whole transcriptome sequencing by analysis of total RNA or mRNA.