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Genomics Analysis System

You have sequencing data and need an analysis others can repeat.

Sequencing produces a great deal of data quickly. Turning it into results that hold up means checking quality, choosing the analysis and documenting every step.

Without that documentation, nobody can repeat the work, including you.

Opening soon

Who it is for

Research groups with sequencing data.

What it aims to improve

A documented analysis that others in your group can repeat.

What it does

This service is planned. The scope and the methods are not fixed yet, so we describe only what we intend to cover.

The right method depends on your research question, study design and data. We support your analysis; scientific responsibility for the results stays with you and your team.

What we plan to include

  • Quality assessment of sequencing data
  • Sequence or variant analysis
  • Reproducible, documented analysis steps
  • Support with interpretation

What is not included

  • Clinical or diagnostic interpretation
  • Sequencing itself
  • Analysing data you have no right to share

What you need to bring

  • The kind of sequencing data you have
  • The question you want to answer with it

Where this service stands

Opening soon

We are finalising this service. Leave your email and we will tell you the day it opens.

Good to know before we start

  • The scope and the methods are not fixed yet. We name no specific tools until they are.
  • No data is sent before a secure transfer method has been agreed.

The next step

Leave your email address and we will write to you the day this service opens. There is nothing to prepare yet.

There is no preparation sheet for this service yet, because it is not open.

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