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DECODR™

Biocomputing made easy and powerful

Accurate. Intuitive. Visual. CRISPR analysis at its full potential.

DECODR™ (Deconvolution of Complex DNA Repair) provides a convenient and user-friendly method to quantify the edits present in CRISPR-edited Sanger sequencing data.

DECODR™ is capable of analyzing a wide range of edits, including:
Insertions or deletions
Combined insertion and deletion events
HDR insertions and single-nucleotide substitutions

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.

DECODR comparison table

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 licensing.decodr@geneeditinginstitute.com

Please visit DECODR.org to register your account and start using DECODR in your lab today. DECODR is also accessible on the LatchBio platform.

Need more information?

To find out more about DECODR, email us at decodr@geneeditinginstitute.com (Non-profit & Academic Interest) or licensing.decodr@geneeditinginstitute.com (For-profit & Commercial Interest).