Pricing Overview
We have experience with a wide range of techniques and the ability to accommodate a variety of projects. As a guide, we have listed pricing below for some of the more common types of sequencing runs. To obtain a quote or discuss a project type that is not listed here, please contact us.
Our bulk RNAseq and miRNAseq pricing includes library prep and sequencing as described. Our DNA library prep pricing only includes library prep, as the required sequencing depth will be project specific. Our nucleic acid extraction services are also listed further down the page.
Bulk Sequencing Service | Sequencing Configuration | <32 Samples | 32+ Samples |
mRNAseq (polyA selection) | 18-20M reads/sample 100SR | $420 | $380 |
Total RNAseq | 25-30M reads/sample 100SR | $450 | $400 |
Paxgene RNAseq (+globin depletion) | 25-30M reads/sample 100SR | $480 | $430 |
miRNAseq | 8-10M reads/sample 100SR | $360 | $340 |
DNA library prep | Library prep only | $65 | $55 |
Our single cell library prep and sequencing services are priced separately as the number of cells captured will affect the required amount of sequencing. Our standard gene expression assay is run using the 5' 10X Genomics method, and the VDJ and Feature Barcode library preps are available as add-on services to a gene expression capture.
Single Cell Sequencing Service | Pricing Unit | Unit Cost |
Gene Expression Capture & Library Prep | Price/capture (up to 10000 cells) | $1,800 |
VDJ Library Prep | Price/capture | $300 |
Feature Barcode Library Prep | Price/capture | $300 |
Sequencing of scRNAseq Gene Expression Libraries | Price/cell(50000 reads/cell) | $0.28 |
Sequencing of VDJ or Feature Barcode Libraries | Price/cell (5000 reads/cell) | $0.03 |
If you would prefer to prepare your own libraries, we also offer a variety of sequencing options. User-prepared libraries must be run separately in their own lane or flowcell.
Run Type | NovaSeq Flowcell | Expected Reads/Run | Cost/Run |
100 cycles (100SR, PE50) | SP | 0.65-0.8 billion reads | $3,400 |
S1 | 1.3-1.6 billion reads | $5,300 | |
S2 | 3.3-4.1 billion reads | $9,400 | |
200 cycles (PE100, PE75) | SP | 0.65-0.8 billion reads | $4,400 |
S1 | 1.3-1.6 billion reads | $6,800 | |
S2 | 3.3-4.1 billion reads | $12,000 | |
S4 | 8-10 billion reads | $17,500 | |
S4 (single lane) | 2-2.5 billion reads | $4,400 | |
300 cycles (PE150) | SP | 0.65-0.8 billion reads | $5,100 |
S1 | 1.3-1.6 billion reads | $7,700 | |
S2 | 3.3-4.1 billion reads | $13,600 | |
S4 | 8-10 billion reads | $20,000 | |
500 cycles (PE250) | SP | 0.65-0.8 billion reads | $7,300 |
MiSeq Run Type | Expected Reads/Run | Cost/Run |
MiSeq v3, 600 cycle kit | Up to 25 million reads | $2,400 |
MiSeq v3, 150 cycle kit | Up to 25 million reads | $1,300 |
MiSeq v2, 500 cycle kit | Up to 15 million reads | $1,800 |
MiSeq v2, 300 cycle kit | Up to 15 million reads | $1,500 |
MiSeq v2, 50 cycle kit | Up to 15 million reads | $1,100 |
MiSeq v2 Micro, 300 cycle kit | Up to 4 million reads | $800 |
MiSeq v2 Nano, 500 cycle kit | Up to 1 million reads | $750 |
MiSeq v2 Nano, 300 cycle kit | Up to 1 million reads | $570 |
These prices include QC via Qubit and Bioanalyzer or TapeStation. *Please note that extraction projects have a six sample minimum.
RNA Extraction Services | Starting Sample Type | Cost/Sample |
Qiagen RNeasy Mini* | Cells/tissue snap frozen or in RLT | $25 |
Qiagen RNeasy Micro* | Cells/tissue snap frozen or in RLT | $28 |
Qiagen miRNeasy Mini/Micro* | Cells/tissue snap frozen or in QIAzol | $25 |
PreAnalytix Paxgene Blood RNA* | Blood in Paxgene RNA tubes | $30 |
We are happy to provide quality control services for various samples that you have prepared yourself. **Please note that Bioanalyzer projects have a six sample minimum.
QC Service Type | Cost/Sample |
Bioanalyzer (RNA Nano or RNA Pico)** | $7 |
Bioanalyzer (High Sensitivity DNA)** | $9 |
TapeStation (RNA, RNA-HS, D5000-HS, D1000-HS, Genomic DNA) | $6 |
Qubit (DNA or RNA) | $3 |
We offer a variety of bioinformatics services to support data generated in our genomics core. This can include a basic alignment and annotation of your sequencing data to produce gene count tables and bam files, or further statistical analyses to identify differentially expressed genes and activated pathways. As the scope of each project can vary widely, we encourage you to contact us for a quote.