We offer comprehensive analysis of sequencing data for a variety of genomics and other sequencing-based experiments.
We accept most types of sequencing data, including Illumina, Oxford Nanopore, PacBio, 454, and Sanger reads, and have experience with a variety of sequencing protocols (RNA-seq, ChIP-seq, Methyl-seq, whole-genome sequencing, whole-exome sequencing, etc). Using the very latest software, we work with you to design custom algorithms and analyses to fit your study needs.
Examples of Analysis:
- Transcriptomics (bulk and single cell RNA-seq)
- ChIP-seq and ATAC-seq analysis
- SNP and structural variant detection
- 16S rRNA analysis
- Methylation – seq
- Custom (includes consultation)
What is the cost for this service?
Prices for individual projects will depend on the size and demands of the project, including the need for designing custom solutions. While we cannot estimate the needs for each type of analysis.
Please contact us for a more specific solution and pricing for your project. If you are preparing a grant proposal, please allow at least one week for a custom quote and to discuss your specific needs and analyses.
I’ve had my consultation, what’s next?
To place your order, follow these steps:
- Click on the link above
- Under the service listing select Computational BioAnalysis
- Click on Initiate Request
- Fill in the form with the details determined during your consultation
- Submit your request
- Don’t worry, if you don’t get everything right, we can change the order later!
Contact us
For more information or to submit a request for analytical services please contact:
Liliana Florea, Ph.D.
Associate Professor
(443)287-5624
