Genomics Core Price List / Orders

To order services from the GMBSR, please click on the Radar button below.


Service List and Pricing - 2023/2024

Prices shown reflect internal Dartmouth rates. External users and those with large projects should contact the core directly for pricing information. Actually prices may vary based on batch size.

All services provided by the GMBSR are supported by an NCI Cancer Center Support Grant (5P30CA023108) which MUST be cited in any publications or other materials using data generated in the core.

Single cell sequencing services are provided through the Single Cell Genomics Core and are subsidized by a COBRE grant (P20GM130454). This grant MUST be cited in all publications and materials using single cell data generated in the core.

DNA/RNA Extraction from Cells/Tissues: $31/sample

Extraction of DNA and/or RNA from cell pellets or tissue chunks. Samples should either be snap frozen on dry ice, or homogenized in Qiagen RLT buffer and stored at -80C prior to processing. Cell input range: 10,000 - 10,000,000 cells. Tissue input range: 1-10mg.

DNA/RNA Extraction from FFPE: $40/sample

Extraction of DNA and/or RNA from FFPE treated samples. Note: Yields from DNA + RNA extraction are expected to be lower than DNA or RNA extraction alone.

Qubit Fluorometer: $2/sample

Specific and accurate quantification of DNA or RNA. Minimum 3ul sample required.

Fragment Analyzer: $6/sample

High resolution sizing of DNA and RNA fragments. DNA size range: 20bp-50Kb. RNA size range: 15nt - 6000nt. Sensitivity down to 200pg/ul.

To assist user in determining the most appropriate RNA-seq workflow for their project we have created tool that can be accessed HERE. It is always recommended to consult with core staff (free-of-charge) before finalizing an RNA-seq experimental design.

Ribodepletion: $196/sample

Provides full-length sequencing coverage for mRNAs as well as long non-coding (lnc) RNAs. Ideal for full transcriptome characterization and is the only RNA-seq option available for prokaryotic samples. Recommended sequencing depth ~30M reads per sample for typical mammalian genomes. Less coverage required for small prokaryotic genomes. Up to 192 samples can be uniquely barcoded for pooled sequencing.

3' End-Counting: $89/sample

Cost-effective option for differential expression analysis from eukaryotic samples. Oligo dT probes are used to capture polyadenylated RNA. Captured RNA is fragmented and the 3' end is selectively amplified by PCR. As most of the reads are associated with 3' UTR sequences, this approach is best suited for organisms with well-annotated genomes (Human, Mouse and Rat). This method cannot be used to identify splice isoforms. Recommended sequencing depth 10M reads per sample. Up to 96 samples can be uniquely barcoded for pooled sequencing.

miRNA/smRNA: $185/sample

miRNAs/smRNAs are too small to be captured by the Ribodepletion, Poly-A and 3' End-Counting workflows described above. This method uses direct ligation of RNA adapters to attach universal sequences to the miRNA/smRNA molecules. These sequences serve as priming sites for PCR amplification and sample barcoding. miRNA/smRNA libraries include Universal Molecular Identifiers (UMIs) to accurately count miRNA/smRNA molecules and minimize PCR bias. Recommended sequencing depth is 1-10M reads per sample. Up to 96 samples can be uniquely barcoded for pooled sequencing.

DNA-seq: $98/sample

Used to prepare sequencing libraries from intact genomic DNA (whole genome sequencing) or sheared DNA (ChIP, CUTNRUN). For intact gDNA, samples are fragmented using a Covaris E220 Evolution sonicator. Adapters are ligated to fragmented DNA molecules and amplified prior to sequencing. Up to 192 samples can be uniquely barcoded for pooled sequencing. Recommended sequencing depth is dependent on application, genome size and desired coverage. Please consult with the core to determine your sequencing requirements. A sequencing coverage calculator is also available HERE.

AmpliSeq: $218/sample

Uses Illumina's AmpliSeq workflow to perform targeted amplification and sequencing of DNA and/or RNA molecules. Illumina supplies off-the-shelf panels or can design custom panels based on user's specifications. Users are responsible for purchasing the primer sets from Illumina while the core supplies reagents for library preparation and QC. Custom panels can be designed and purchased using Illumina's DesignStudio software, while ready-to-order panels are available HERE.

Target Capture (Exome Sequencing): $148($248)/sample

For large targeted sequencing studies, including whole exome sequencing, target capture methods are preferred over PCR-based approaches. This is due to the challenge of designing large pools of primers with minimal off-target amplification and coverage bias. We use IDT xGen target capture reagents to provide custom target capture as well as whole exome solutions to our users. For custom panels, users should use the IDT Design Tool to create and order their panels. IDT's Exome v2 panel is stocked by the core and is included in the exome sequencing price listed above.

Single cell genomics experiments are complex and require tight coordination between the researcher and our core. Consultation with core staff is required before projects are accepted and is provided free-of-charge. Services listed include the cost of sample QC using an automated fluorescent cell counter (Nexcellom K2) as well as all downstream library preparation and QC steps.

For all 10x genomics workflows, a "sample" is equivalent to one lane on the 10x instrument. Each lane can capture between 100-10,000 cells, depending on the concentration loaded onto the instrument.

A cost calculator is provided HERE to help budget for single cell experiments.

Sample Fixation for 10x Genomics Flex: $122/sample

Samples are provided as cell suspensions or tissues for fixation following the 10x Genomics Flex protocol. Cells are stored at -80C in the GMBSR until ready for processing within 1 year.

Tissue Processing for 10x Genomics: $222/sample

  • Nuclei isolation from fresh/frozen tissue
  • Tissue dissociation into single cell suspension (Off the shelf protocols available for some tissues. Those requiring optimization may incur additional charges.)

10x 3'/5' RNA-seq: $2,216/sample

Uses the 10x Genomics workflows for 3' and 5'-End RNA-seq. For standard gene expression measurements, 3' RNA-seq is the standard in the field. 5' RNA-seq is required where TCR and/or BCR (i.e. V(D)J) sequencing is performed. Up to 96 unique barcodes are available for pooled sequencing. Recommended sequencing depth is 30,000 reads per cell, but will vary depending on the RNA content of the cell type(s) to be analyzed.

10x Library Add-On: $348/library

Additional modalities can be applied to 10x RNA-seq samples to generate multi-omics datasets at single cell resolution. These include TCR/BCR sequencing, proteomic analyses (i.e. CITE-seq), sample multiplexing (via MULTI-seq or Total-seq) and other custom assays. For each additional modality, a Library Add-On is required per sample. Additional sequencing is also required, typically 5,000 reads per cell per library type.

10x Gene Expression Flex (AKA Fixed RNA Profiling): Variable (See below)

The Flex assay enables single cell RNA-seq analysis of Human or Mouse cells or tissues that have been fixed following one of the 10x Demonstrated Protocols. Samples can be stored at -80C for up to 6 months. If  samples are prepared in the GMBSR, -80C storage costs are included. Once collected, samples can be thawed, uniquely barcoded and combined together onto a single 10x lane for processing. Pooling configurations and pricing are as follows:

    • 1 Barcode: $2,960/lane
    • 4 Barcodes: $4,885/lane
    • 16 Barcodes: $10,035/lane

Recommended sequencing depth is 20,000 reads/cell.

10x ATAC-seq: $2,369/sample  

The 10x ATAC-seq workflow interrogates regions of open chromatin at single cell resolution. As for all single cell experiments, users provide a viable single cell suspension and the core performs all downstream processing steps. For ATAC-seq, this includes sample QC, nuclei isolation/permeabilization, DNA transposition, cell capture and library preparation. Up to 96 unique barcodes are available for pooled sequencing. Recommended sequencing depth is 25,000 reads per cell.

10x Multiome (RNA+ATAC): $3,807/sample

The Multiome workflow generates paired RNA-seq and ATAC-seq data from the same nuclei in a given sample. Specific requirements exist for preparing nuclei suspensions for this assay this is included in the cost of the service. Users interested in providing their own nuclei suspensions should consult the GMBSR and 10x Genomics website for appropriate procedures. Sequencing requirements are 25,000 reads per cell each for RNA and ATAC datasets (50,000 reads/cell total).

10x Instrument Training: FREE

The genomics core staff are available between 8am and 5pm, Monday-Friday to perform 10x experiments. Should users need access to the instrument outside these hours, they can be trained to operate the instrument independently. Training takes ~2 hours and includes a discussion of the principles of the 10x workflow as well as hands on time with the instrument using "dummy" reagents. Trained users will be provided access to the lab as well as the instrument reservation calendar via RaDar.

Illumina Methylation EPIC: $310/sample

The Illumina Methylation EPIC array profiles over 850,000 CpG and non-CpG sites throughout the human genome to provide quantitative DNA methylation data for differential methylation analysis. Service includes input DNA quantification, bisulfite conversion array labeling, scanning and data delivery. Arrays consist of 8 samples each and must be in full.

FFPE Restoration for Illumina Methylation EPIC: $139/sample

Analysis of FFPE samples on the Illumina Methylation EPIC arrays requires DNA restoration to provide sufficient DNA quality and quantity for analysis. A qPCR assay is used to generate a quality score for all FFPE DNA samples submitted for this service. Samples with acceptable quality scores proceed to restoration and the remainder of the array preparation workflow. Samples with low quality scores will be reviewed with the user to determine the best course of action.

Preparation of Customer-Ordered Illumina Infinium Arrays: $80/sample

Illumina manufactures arrays for targeted genomic profiling of samples from a wide variety of species. A complete list of available arrays can be found HERE. Users are responsible for ordering arrays from Illumina and the core will perform DNA quantification, array labeling, scanning and data delivery.

Prices for Illumina sequencing include library normalization, pooling, sequencing and raw data storage for 5 years. FASTQ files are stored on Dartmouth's DartFS storage system which is accessible to the entire Dartmouth community. If you need a DartFS account, please contact Research Computing. Please let us know if you need to share data with an external collaborator and we can make the data available for secure download via a web server.

All Illumina sequencing kits can be run in single-end or paired-end configurations. Sequencing can be purchased as entire flow cells, or on a per-read basis, assuming available space for shared sequencing runs. NovaSeq runs must be purchased as full flow cells. Most common flow cells are shown with others available upon request.

Sequencing Platform Flow Cell Number of Reads Cycles Price
NextSeq2000 P1 100M 100 $1,170
300 $1,540
600 $2,218
P2 400M 100 $1,738
200 Contact for pricing
300 $4,365
600 Contact for pricing
P3 1.2B 100 $3,640
200 $4,936
300 Contact for pricing
NovaSeq6000 SP 800M 300 $3,615
S1 1.5B 300 $6,185
S2 4B 100 $8,397
300 $11,172
S4 9B 300 $18,329