Illumina High Throughput Sequencing Services

Introduction

Illumina sequencing platforms generate up to 800 gigabases of high-quality sequence data per lane (NovaSeq 6000 S4) using a massively parallel short-read sequencing approach. The Illumina systems use sequencing-by-synthesis technology and reversible terminator chemistry.

Summary

We are also sequencing on the NovaSeq 6000.
Steps involved in an Illumina sequencing experiment can be broken down into a series of experimental manipulations, instrument runs, and data analyses. These steps include creation of sequencing libraries, seeding clustering of the flow cell on the sequencer, sequencing by synthesis, and bioinformatics.

Sample Submission

We must receive electronic and print copies of the appropriate submission form in order to receive and schedule your samples.

CD Genomics has already updated its technology platforms to mainstream NGS, long-read sequencing, and microarray instruments. We continue to strive to offer the same reliable services to pharmaceutical and biotechnology companies, as well as academia and government agencies, for all your sequencing or array needs. If you are interested, please contact us directly for assistance.