NGS of DNA from RNAi Screen, > 100M reads-commercial accounts

Description

Full Service for samples from your shRNA library screen

If you are running genetic screens with a Cellecta CRISPR shRNA library, just provide genomic DNA for each time point or treatment condition (one sample), and we will provide you with a spreadsheet enumerating the read number for each of the library elements.

Service description:

– shRNA-cassette amplification
– NGS-library preparation
– NGS on the Illumina NextSeq or HiSeq platform (100M reads)
– Deconvolution
– Enumeration of shRNA counts from raw sequencing data including statistical report

Additional bioinformatics and pathway analysis are available on request.

You can also send cells or tissue samples obtained in your screens and Cellecta will perform the genomic DNA extraction for an additional fee.

Bulk prices for multiple samples are available. Please use our service request form to contact us for more details.