The majority of molecules sequenced are uninformative.
We're changing that.
~66%
of the human genome is repetitive DNA
~90%
of reads from a single cell data set are noise
100%
increase in reads mapping to the transcriptome with CRISPRclean Single Cell RNA Boost
Improve sensitivity
Get 1.5x improvement in gene and UMI detection sensitivity and gain a deeper view of individual cells
Double your data
Achieve a 100% increase in informative transcriptomic reads with typical read depths
CRISPRclean technology
Our mission is to cut through the noise with solutions to see the information you really want—bringing
an end to wasted sequencing reads and uninformative data. CRISPRclean technology allows you to
harness the specificity of CRISPR to refine NGS libraries to deplete those abundant sequences.
See how CRISPRclean works
Applications
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