DNA-seq Service (Genetic Screens)

DNA-seq service for pooled CRISPR and shRNA screen library prep and analysis

When you have run a pooled CRISPR or shRNA screen and need to convert genomic DNA into a barcode-count table, this service handles library prep, sequencing, and analysis deliverables. Removes the in-house bottleneck of screen-specific NGS workflow setup.

Pick by screen format and turnaround.

1. Screen format. The service must support your library type and indexing scheme. Backbone-matched indexing primers are essential.
2. Turnaround. 4 to 8 weeks from sample receipt is typical.
3. Bioinformatics deliverables. Confirm whether the service delivers raw FASTQ, count tables, or full hit-calling analysis.
4. Sample input flexibility. Verify low-input compatibility if your samples need it.
5. Use case. For one-off screens outsourcing avoids the steep learning curve. For screen-heavy labs in-house workflow is more cost-effective long-term.

Cellecta supplies DNA-seq services in this inventory, paired with their library platforms.