email: contact@intelliseq.com

Bioinformatic Products. Bioinformatics Services.  R&D.

DNA Analysis made simple

bioinformatic tools for genome-based medicine.

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IntelliseqFlow

Software as a service platform for NGS data analysis requiring no upfront cost. IntelliseqFlow takes your WGS or WES samples from raw data to automatic and complete report with clinical insights.

How it works:

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Step I

Create an account and easily upload to catalogue your sample with raw NGS data

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Step II

Choose 1 out of 100+ Workflows, manage input and output files. Run analysis.

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Step III

Check the analysis progress on your dashboard and results when completed. Make decisions based on the complete report. 

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Secure

Data is encrypted and we are HIPAA complaint.

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Intuitive

Simple to use, designed by scientists for scientists.

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Fast

Few steps and bit of time from data to result

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SaaS

Software as a service platform with no installation needed.

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Elastic

Integration with LIMS, custom installations, white-label.

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Complete Workflows

100+ Workflows available, from simple to complex.​

How can we help you?

Intelliseq is a team of experienced scientist, geneticists, bioinformaticians and software engineers. We have already solved many problems for our clients globally. Let us help you with yours.

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Custom NGS data analysis

Being scientists and doctors ourselves, we know that even advanced bioinformatics software for data analysis is sometimes not enough. Some genetics projects are of high data volume; the others are more complex and demand custom bioinformatic analysis with individual attendance and in-depth attitude. Intelliseq responds to the expectations and provides advanced analysis and development services for clients requiring more.

Our custom services include:

  • Icon_LICreated with Sketch. Advanced identification of genetic variants,
  • Icon_LICreated with Sketch. Functional and clinical annotation of genetic variants,
  • Icon_LICreated with Sketch. Qualitative and quantitative analysis of the transcriptome,
  • Icon_LICreated with Sketch. Analysis of copy number variants(CNV),
  • Icon_LICreated with Sketch. De novo assembly of the entire genome or transcriptome.
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Research & Development

Our products and services are the result of advanced and in-depth research and development activities.

We try not only to follow the path, but also uncover new ones.

Genetraps

automatic genome interpretation software for  reporting multiple diagnostic traits 

Mobigen

Innovative mobile application for consumer genomics

PGx

development and validation of the software system for pharmacogenomics

Trusted us

Learn more about our partners and their use cases from the collaboration.

THE JOHN PAUL II HOSPITAL

One of the Intelliseq clients is a healthcare facility, which either uses IntelliseqFlow or cooperates with our team in large projects. 

Our Blog

Partnership for Innovation

Attending the “Partnership for Innovation” conference. Our representatives, Klaudia and Michał, took part in the “Partnership

January 15, 2020

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