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RNAseq via ribodepletion

Engineering Plans

Learn more

RNA-seq will be applied to quantify the gene expression patterns of human tissue, blood, plasma or cells as well as identify gene fusions. This will allow for the identification of cell types present in a sample, characterization and quantification of cell type specific expression patterns and study phenotypic differences between tissue/cell types, different treatment conditions and healthy vs disease.

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Sample types

Blood > RNA

PAXgene Blood RNA tube

10 ml (2,5 ml blood)

Ice pack

Blood > cfRNA/exoRNA

Streck RNA Complete BCT

10 ml

Room temperature

Cells of various tissue origins > RNA

Microtube* with cells on lysis buffer

> 5 million cells

Dry ice

FFPE block of various tissues > RNA

Paraffin block (in cassette)

Representative block ; Tumor load preferentially >10% ; To be processed by our pathology department (microtome section needed)

Room temperature

FFPE section of various tissues > RNA

Microtube*

Min. 1x 10 µm section (up to 2 mm³ tissue) ; Tumor load preferentially >10%

Room temperature

Plasma > cfRNA/exoRNA

DNA LoBind 5 ml tube

> 2ml

Dry ice

RNA from various tissues > RNA

Microtube*

See test details/specifications

Ice (max. 20 min) or dry ice

RNA from various tissues > RNA

Microtube* or 96 well plate

See test details/specifications

Ice (max. 20 min) or dry ice

Tissue of various origins > RNA

Cryovial containing stabilizer (eg. RNAlater) or tissue homogenized on lysis buffer

Application/tissue specific (contact us)

Dry ice

Extra requirements

Minimum DV200
RNA tube & plate - Diagnostic

Minimum: 30 %

Below a DV200 of 30% we experience lower yields or total library prep failure. Please provide us with a new sample if this requirement is not met.

Absorbance ratio A260/A230 - Minimum
RNA tube & plate - Diagnostic

Minimum: 1,5

Lower values are indicative for indicative for EDTA, carbohydrate, chaotropic salts (and also protein) contamination

Absorbance ratio A260/A280 - Minimum
RNA tube & plate - Diagnostic

Minimum: 1,5

Lower values are indicative for indicative for protein, phenol or other aromatic compound contamination

Elution buffer : nuclease free water
RNA tube & plate - Diagnostic

:

Please use nuclease free water as an elution buffer for your RNA samples. Other buffers (e.g. containing EDTA) may inadvertently affect our assays

Minimum RNA quantity
RNA tube & plate - Diagnostic

Minimum: 200 ng

Below 40 ng of input, success rate is very low without adjusting PCR cycles. Please provide us with as much as material as possible (200 ng preferred).

Image by Mezidi Zineb
Sample types
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Deliverables

Below, you can find the type of data files that can be retrieved for this test.

If you require more information or need a more custom output, please consult our Bioinformatics page.

Run folder

The complete run folder can be transferred if it concerns a run reservation (private run)

RUO (on request)
Deliverables

Costs

Below, you can find indicative prices (excl. VAT) for all potential options you'd require to accomplish your project. If you are interested, please contact us to receive a tailored quotation.

Update pending

Our prices are being updated. More info soon.

Euro Bill
Costs
Books

Documents & certificates

Validated
Validated
Documents
Plan Experiment

Plan experiment

  1. For Diagnostics

This test is also performed as a diagnostic assay. In this case, please contact your General Practitioner, Pathologist, haematologist or Clinical Geneticist (Centre for Medical Genetics or haematology department of choice) to get the diagnosis started.


  1. For Research

This test can also be applied in context of research. For this, please get approval from your local ethical committee and/or make proper arrangements with your Biobank.

Please follow the steps below to start up an experiment with us.

Get in touch (ONLY FOR NEW PROJECTS)

Explain your project, so we can assist you to find the best solution.

Expect questions like :

  1. What type of sample would you like to analyze?

  2. Which elution buffer did you use?

  3. What are the expected concentrations of your samples?

  4. How many samples would you like to process?

  5. How fast do you need the results (TAT) and/or do we need to expedite?

  6. If you deviate from our sample types, are there test samples available?

  7. Are our standard deliverables ok?

  8. ...

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1

Request quotation

Once you know which experiment you want to set up, fill out the 'Quote request' form, with the essential details of your project :

  1. Coordinates of the person to whom to address the quotation

  2. Which type of test you'd like to set up

  3. Do you require a specific deliverable?

  4. Do we need to expedite (comes at extra cost)?

  5. ...

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2

Submit your samples

Once you agree with our terms (quote / TAT / terms & conditions)  :

  1. Fill out our sample submission form

  2. Send it via email : contact us

  3. Print out the form and include it with your samples

  4. Send your samples to us

  5. Label your tubes/plates correctly : see details here

  6. Adhere to the corresponding transport conditions listed under Sample types

  7. Indicate if we can discard your samples after completion of project

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3

Your experiment starts

Now it is up to us... We will start your experiment as soon as possible.

  1. When expedited, the turn-around-time (TAT) is 2,5 weeks

  2. For standard requests the turn-around-time (TAT) is 2 months


The standard TAT is generally overestimated, but this extended timeframe allows us to : combine similar requests of multiple scientists and to repeat the experiment in case of issues.


Please refrain from contacting us in case the pre-agreed TAT didn't expire yet.

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BRIGHTcore / T +32 (0)2 477 64 79 / F +32 (0)2 477 68 59

Photography / See our Colofon

Content & illustrations / Ben Caljon

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