For a consultation and quote: email or call +1-206-732-6068.

 CUSTOM SEQUENCING SOLUTIONS

Seattle Genomics, a service core at the University of Washington offers next-generation sequencing and data analysis solutions.
The center is a component of the Washington National Primate Research Center and is operated by the Division of NHP Systems Biology in the Gale laboratory.

Services and Rates

We offer the following:

Illumina NextSeq 500 and Miseq
DNA/RNA library preparation and QC
Purified PCR products
Microarray processing
Bioinformatics analysis and support
RNA Isolation and QC

mRNA-seq

For example, for 20 samples to have RNA isolated from tissue, mRNA-Seq libraries constructed with Illumina’s TruSeq mRNA Library Preparation Kit, and sequenced on our NextSeq 500 using a high output 150 cycle (paired end 75bp), the total cost would be $8,238.02, which averages to $411.90 per sample including taxes. This run will produce approximately 20 million reads per sample.

Total RNA-seq

For example, for 20 samples to have RNA isolated from tissue, Total RNA-Seq libraries constructed with KAPA’s Stranded RNA-Seq Kit with RiboErase (HMR), and sequenced on our NextSeq 500 using a high output 150 cycle (paired end 75bp), the total cost would be $12,877.04 which averages to $643.85 per sample including taxes. This run will produce approximately 40 million reads per sample.

Custom applications REQUIRE consultation to discuss project.


Sequencing Run Costs

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Library and QC Costs

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RNA Extraction and QC Costs

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RNA-seq

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Microarray

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Microbiome

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DNA-seq

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Data Analysis and Delivery

For file delivery and analysis, we offer multiple options to suit the specific needs of the end user.

An  link will be provided to download all of the raw (FASTQ) files and QC summaries.  Data can also be shared via BaseSpace. This, as well as a summary of read and run QC is provided as part of the sequencing cost.
For customers desiring a more complex and comprehensive bioinformatics analysis and processing a free consultation up to 2 hours will be provided prior to any sample processing or sequencing.  This consultation is mandatory for this type of analysis to ensure the numbersof samples and comparisons are adequate for the types of analysis desired


Analysis tier 1:

Mapping to a supplied genome/reference with or without annotation, and results in a delivery of a BAM/SAM file to the customer.  This BAM/SAM file can then be used for the next steps of data processing and analysis.


Analysis tier 2:

Targeted to users without sufficient computing resources for data processing, but which have expertise and access to bioinformatics tools for downstream functional analysis and interpretation. For RNA-seq data, raw data matrix as well as differential expression analysis will be provided to the user. For host or pathogen genetic analysis, alignments and variant files will be provided. Users will be responsible for downstream analysis.


Analysis tier 3:

Targeted to users without sufficient computing or expertise in downstream analysis and interpretation. These interactions will be more collaborative in nature. We will consult with the user to define a plan that will include any required aspects of a project, from library preparation to downstream analysis.   For RNA-seq, the user will be provided with transcript quantification and the raw data matrix as well as functional analysis based upon their specific biological questions. If necessary, we will also provide de novo assembly of transcriptome or virus genome where a specified reference is not available.


Pricing is for up to 24 samples, and tier 3 will require a custom price quote based on FTE hour units and computation units of use (CPU hours/disk storage).  There is a minimum charge of 40 hours for up to 24 samples for this tier.

Analysis Tier 1:  $2000
Analysis Tier 2:  $3000
Analysis Tier 3:  $6000 plus additional rate of $115/hr.


Requesting Sequencing Services

  1. Obtain a quote using our online form.
  2. Prepare your samples or libraries for submission.
  3. Ship or drop of your samples to the address below.
  4. We will e-mail confirmation of receipt and what services will be performed.
  5. Await a sequencing report at the end of sequencing project, with directions on how to get data from BaseSpace if not locally delivered.

We will store locally all sequence and run data for 3 months.

 

Sample and Library Submission Guidelines

Locally libraries can be delivered to the adress below. For shipping please contact us first for guidelines and further instructions.

Shipping Samples

Seattle Genomics
c/o Elise Smith Rm 252
Rosen Building
960 Republican St.
Seattle, WA 98109-4325
(206)732-6068



University of Washington logo


Request a quote

mRNA-seq

For example, for 20 samples to have RNA isolated from tissue, mRNA-Seq libraries constructed with Illumina’s TruSeq mRNA Library Preparation Kit, and sequenced on our NextSeq 500 using a high output 150 cycle (paired end 75bp), the total cost would be $8,238.02, which averages to $411.90 per sample including taxes. This run will produce approximately 20 million reads per sample.

Total RNA-seq

For example, for 20 samples to have RNA isolated from tissue, Total RNA-Seq libraries constructed with KAPA’s Stranded RNA-Seq Kit with RiboErase (HMR), and sequenced on our NextSeq 500 using a high output 150 cycle (paired end 75bp), the total cost would be $12,877.04 which averages to $643.85 per sample including taxes. This run will produce approximately 40 million reads per sample.


Your Name*
Your Email*
If Academic , Principal Investigator(PI)
Company
If UW, Department
CIIID member? (Yes or No)
How many samples?
Budget Number
Processing Platform

If other please enter in the text field below.
Will you be requiring analysis/Bioinformatics support?

* required

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