The Integrated Genomics Center (IGC) provides comprehensive next-generation sequencing (NGS) library preparation services supporting a wide range of genomic, transcriptomic, epigenomic, and single-cell applications.
Our teams provide consultative support for assay selection, experimental design, library preparation, sequencing strategy, and downstream data analysis across both standard and highly specialized workflows. Services support diverse sample types including high-quality and degraded RNA, FFPE specimens, low-input DNA, cfDNA, microbiome samples, and long-read sequencing applications.
By integrating library preparation, sequencing, and computational analysis within a unified genomics environment, the IGC enables investigators to access scalable, high-quality workflows tailored to the needs of modern translational and biomedical research.
Organization by Application Category
RNA Sequencing
- bulk RNA-seq
- total RNA
- RNA exome
- low-input RNA
- SMART-seq
- miRNA
- 3’RNAseq
DNA Sequencing
- WGS
- low-input DNA
- FFPE
- cfDNA
- methylation/WGBS
Epigenomics & Chromatin
- ChIP-seq
- ATAC-seq
- CUT&RUN
Long Read Sequencing
- PacBio HiFi
- Kinnex
- Oxford Nanopore Technologies (ONT)
Specialized Applications
- microbiome
- custom Ion Torrent
- scRNAseq
| Application | Available Workflows |
|---|---|
| Bulk RNA-seq | Total RNA RNA Exome SMART-seq QuantSeq |
| DNA-seq | Low-input Whole Genome Sequencing (WGS) Whole Exome cfDNA FFPE |
| Epigenomics | Whole Genome Bisulfite Sequencing (WGBS) ChIP-seq ATAC-seq CUT&RUN |
| Long-read | Oxford Nanopore Technologies (ONT) PacBio Whole Genome Sequencing PacBio Kinnex |
Ready to Begin? Book a Consultation to Plan Your Order
Not sure which workflow is right for your project? IGC scientists are available to assist investigators with:
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- assay selection
- experimental design
- sample quality assessment
- sequencing strategy
- workflow optimization
- bioinformatics planning
- data analysis considerations
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