Accurate. Intuitive. Visual. CRISPR analysis at its full potential.
DECODR uses a computationally efficient algorithm and provides the identity of deleted and inserted bases with no limit on insertion and deletion size. DECODRTM supports batch analysis, in which several sequencing files can be analyzed simultaneously.
To use DECODRTM, all you need are Sanger sequencing files from your experimental samples. You upload the sequence files to DECODRTM via drag-and-drop and provide experimental details. DECODR will provide you with NGS-level data output about your CRISPR edits in just seconds.
For more information about DECODRTM see our publication in The CRISPR Journal.
DECODRTM is available to all non-profit and academic researchers. For-profit users and commercial interest in DECODR can contact us at firstname.lastname@example.org