CNOverview
Comprehensively covers the CDS regions of the whole transcriptome, incorporates key UTR regions related to fusions after in-depth screening, and adds edge probes on both sides of exons to ensure the capture capability of exon boundaries. Additionally, it is engineered at the design level to eliminate rRNA and globin sequences, reducing redundant data and improving utilization efficiency.
It retains the high sensitivity and efficiency of targeted enrichment while possessing the discovery capability of whole transcriptome sequencing, enabling accurate targeting of key transcripts. It assists researchers in in-depth exploration of gene transcription mechanisms and holds significant application value in fields such as cancer gene fusion detection and research on pathogenic mechanisms of rare diseases.
