From library preparation to producing high quality sequencing data, we offer a variety of sequencing services to meet today’s fast-paced research environment.
Human Whole Genome
Whole genome sequencing service includes sample QC, library preparation, and deep coverage sequencing that can be scaled according to the needs of the project.
Exome enrichment focuses on the coding regions of the genome and is a cost-effective alternative to whole genome sequencing. Exome sequencing captures 50 Mbp of coding exonic regions with high specificity and coverage.
Analyzing the transcriptome with mRNA-focused sequencing provides researchers with information to characterize gene expression, gene fusions, alternative splicing, and novel transcripts. Standard coverage ranges from ~20-50 million reads and can be scaled to meet specific project objectives.
Targeted Resequencing and Custom Enrichment
Isolating genomic regions of interest with targeted gene enrichment panels allows for cost-effective, focused detection of germline and somatic mutations. Pre-defined cancer panels cover over 300 cancer-related genes with high specificity and deep coverage. Custom gene panels can also be designed to meet specific project objectives.
Methyl-seq, ChIP-seq, and miRNA-seq services are also available. Please inquire for more details.
We can also sequence your pre-made Illumina-compatible libraries. The HiSeq 2500 High-Output mode is priced on per lane basis whereas the HiSeq 2500 Rapid mode and MiSeq are priced on a per run basis.
Illumina HiSeq 2500 High-Output
High-output mode can generate up to 180 million reads per lane with single read sequencing and up to 360 million reads per lane with paired-end sequencing.
Illumina HiSeq 2500 Rapid
Rapid mode can generate up to 300 million reads per run with single read sequencing and up to 600 million reads per run with paired-end sequencing and offers rapid turnaround time.
Ideal for small scale projects with rapid turnaround time. In a single run the MiSeq can generate 12-15 million reads with single read sequencing or 24-30 million reads with paired-end sequencing.
The JWCI Sequencing Center is an Illumina Propel-Certified Service Provider, one of a few select laboratories in a collaborative service partnership with Illumina that have demonstrated proficiency in next generation sequencing at the highest industry standard.
Please contact us if you would like to learn more about any of our services.