Deconvolution of Complex DNA Repair:
Near-NGS-level CRISPR editing analysis.
Upload your Sanger files and receive results in seconds.
®
Near-NGS-level CRISPR editing analysis.
Upload your Sanger files and receive results in seconds.
Deconvolution of Complex DNA Repair
“Notably,
Consequently,
DECODR exhibited superior prediction accuracy
DECODR is currently the preferred choice
across most samples, particularly when the samples contained a high percentage of indels.
for Sanger sequencing-based indel frequency analysis, especially when the expected indels exceed the detection size limits of TIDE (-50/+50) and ICE (-30/+14)."
DECODR by the numbers
4000+
Total Users
350+
Peer-reviewed Citations
Experimental Files
1.8M+
DECODR
Analysis
Capabilities
DECODR provides a convenient, cost-effective, and user-friendly method to quantify the edits present in CRISPR-edited Sanger sequencing data.
Using a computationally-efficient algorithm, DECODR has virtually no limit on indel size and can determine the identity of inserted bases. DECODR supports batch analysis, in which several sequencing files can be analyzed at a time.
Sign up today to upload your sequences to DECODR and receive NGS-level results in seconds.
Single &
Multi-guide Analysis
Analyze outcomes from single or duplexed CRISPR experiments without limits on indel size
Compound
Indel Analysis
Analyze complex, combined insertion and deletion events
> 100 bp Indel Analysis Capability
Bulk Population & Clonal Analysis
Analyze pooled cells for full spectrum of outcomes or clonal populations for allelic inferencing
HDR Knock-in
& Substitution Analysis
Identify successful and partial HDR outcomes
Only DECODR supports analysis of indels exceeding 100 bp
$5,299
10,000 files
$0.53 USD per file
Analysis history
storage included
Basic
$0
20 files/month limit
No analysis history
included
Plus
$1,199
1,200 files
$0.99 USD per file
Analysis history
storage included
DECODR
Features &
Pricing
Pro
Power*
$2,799
4,000 files
$0.70 USD per file
Analysis history
storage included
Industry-Leading
Trace Analysis Technology
Batch analysis
Clonal/Bulk analysis of KO indels
Clonal/Bulk analysis of HDR recombination
Multi-guide analysis
Insertion probabilities
Compound indels (insertions & deletions)
Indel analysis >100 bp
Guideless analysis
Paired-end analysis
Chromatogram visualization
Flexible input format (.ab1/.txt/.fasta)
One-click shareable outputs
Pipeline-friendly batch upload
Account-based analysis history
Dedicated support & troubleshooting