To address the emerging needs of the research community,
the CCIB DNA Core is continuously expanding its diverse portfolio of genomics solutions.
In support of the scientific community's enthusiastic embracement of the CRISPR/Cas9 genome editing
technology, we have developed a cost-effective, high-throughput strategy for identifying
CRISPR/Cas-induced mutations via deep sequencing of PCR amplicons.
We are offering this service on a weekly basis.
Start of Next Service Cycle:
Samples must be received at the core facility
no later than 4 pm on Wednesday, . If you are using one of our dropbox locations for sample delivery, please place the order in the cooler by Wednesday mid-morning to ensure timely delivery.
If you should miss the deadline or if the total customer order volume exceeds
our current production capacity, your samples will be entered into the queue and
processed in the subsequent run. Results for all samples processed in our weekly run will
be available within 5 to 8 business days after the start of the service cycle.
Cost-effective ultra-deep sequencing of amplicons derived from CRISPR-targeted genomic regions
Highly sensitive detection of CRISPR-Cas9 induced mutations
CRISPR variant calling
No need for universal tags on target-specific amplicons
No need for time-consuming cloning steps
Sample multiplexing using validated indices
Highest possible data quality
- Fast turnaround time
CRISPR Amplicon Sequencing Details
- The site of interest (i.e CRISPR cut site) must be within the first
100 base pairs of the amplicon (from either the 5'-end or the 3'-end) to ensure high quality data.
Both the NGS adaptors and a unique barcode will be added as part of our NGS sample preparation process.
- Our current approach has been designed to generate complete sequence coverage for 200-280 bp
amplicons. If the identification of amplification primer binding sites should present a problem
for designing amplicons of this size, the submission of longer amplicons (up to 500 bp)
will be acceptable.
In this case, however, only the 5'-end and 3'-end of the amplicon will be covered by NGS reads, i.e. the middle of the amplicon will have a gap (represented by NNNNNNN....).
To obtain complete sequence coverage of 400-600 bp CRISPR amplicons, please submit your sample(s) for our
Complete Amplicon Sequencing
Please contact us
to discuss your specific project needs.
Our guidelines for amplicon design, sample preparation and submission can be found under the section
A short description of our algorithm used to perform CRISPR variant detection can be found
If you should have any additional questions about our CRISPR Sequencing service,
please contact the Core Director.