• Genomics Core Sample Submission Form

  • Please submit the samples in nuclease-free 1.5 mL Eppendorf tubes. There is freezer for sample drop off in SMHS W116 If this is not possible or you have questions please talk to the Core lab. We try and fill QC chips so there may be a delay in results. The 2019 Core website has the prices listed.  If you need a quote contact the Core. If you have a lot of samples you can dowload the excel sheet found on this page under Sample submission item 3, fill it out and upload it with the form. You will still have to add one sample to the form below. 

    User-Prepared Libraries

    Please submit ≥ 10 µL of your undiluted 10 nM library suspended in 10 mM Tris-HCl, pH 8.5. All prepared libraries will be quality checked using the Agilent 2100 Bioanalyzer or Agilent 4200 Tapestation.

    Small Genomes (i.e. Bacteria/Fungi) can be sequenced on the Miseq. Sequencing of larger genomes (i.e. Human/Mouse and Infindium Methlyation Arrays) will be outsourced. 

    DNA Samples

    Please submit ≥ 1 µg of high quality DNA with a concentration of > 50 ng/µL. DNA will be quantified using the Qubit 2.0 fluorometer. 

    RNA Samples

    Please submit ≥ 1 µg of total RNA with a concentration of at least 50 ng/µL. RNA will be quantified using the Qubit 2.0 fluorometer and RNA integrity assessed using the Agilent 2100 Bioanalyzer.

  • Are you from UND or another facility
  • Project Type

  • What sample type are you submitting

  • What is the species of your sample? If you are submitting more than one organism type, please select all that apply.*


  • If you are submitting total RNA or mRNA, have your samples been DNAse-treated?*
  • What nucleic acid isolation method did you use? If a kit was used, please list it below.*

  • Have your samples been purified? If 'yes', please list the method or kit used below.*

  • Are you needing the Core to extract DNA/RNA?
  • If yes to Extraction, what kit do you want
  • What are your samples resuspended in?*

  • Have you quantified your samples?*
  • Please select the method of quantification used.*

  • Are you needing the Core to make libraries?*

  • Library type requested
  • What type of sequencing run are you requesting?*
  • What read length are you requesting?

  • If there are no other samples to fill the chip are you willing to wait or continue and pay for the chip?*

  • Are you wanting a price quote for the project? * note QC prices depend on number of spaces filled.*
  • Are you needing primary Bioinformatic help for sequenced data?

  • For secondary analysis, please fill out the Secondary Analysis Jotform found on this link or on the UND Genomics Website under the Bioinformatics tab. Each project is considered closed after the primary analysis is done and all secondary analysis work is considered a different project. 

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  • The location for sample drop off is in SMHS W116. There is a freezer just to the right when you enter. Please up the samples in a box and label the box with tape. If you have notes you want to write there is a notepad under the freezer. If you wish to discuss the samples with the Core, please email to set up a time. You can email the Core when samples are dropped off to let them know otherwise the freezer will be checked regularitly. 

  • For the labs that have used the UND Genomics Core in any way, please acknowledge us for publications. "Research reported in this publication was supported by the National Institute of General Medical Sciences of the National Institutes of Health under Award Number U54GM128729 and Award number 2P20GM104360-06A1."

  • Data Sharing Policy

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