Intelliseq | DNA analysis made simple

Bioinformatics products. Bioinformatics services. R&D.

Intuitive cloud-based platform for NGS data analysis

We deliver a scalable and lab-friendly platform for genome data analysis with no upfront cost.

Built by engineers, trusted by industry specialists

saas platform We developed an automatic genome interpretation platform for next-generation genome sequencing (NGS) data. IntelliseqFlow platform generates complete reports with clinical insights for doctors, genetic counselors or patients, depending on the chosen workflow.

Our drop-in solution fits all NGS analysis approaches:

From a single gene to a whole genome Genetic diseases Carrier screening Hereditary and somatic cancer Pharmacogenetics Research

How it works

Step I. Create an account and easily upload your sample with raw NGS data.

Step II. Choose 1 out of 100+ Workflows, manage input and run analysis.

Step III. Check the analysis progress on your dashboard and results when completed. Make decisions based on the clinical insight report.

Watch our video presenting the main advantages of the IntelliseqFlow platform.

The IntelliseqFlow platform has a very intuitive interface and allows for a quick and precise analysis of NGS samples. It does not require bioinformatics skills from its users and it accelerates the process of diagnosis in a cost- and time-efficient way. The user pays only per analysis, there are no upfront costs nor installation required or cost of high-power computer facilities. The program runs on its own servers. The reports generated via IntelliseqFlow platform covered the information about variant pathogenicity necessary for the diagnosis of hereditary disorders among our patients.

Center for Medical Genetics GENESIS
Intelliseq has completed a number of orders for OpenExome (currently AnalitykGenetyka) regarding sequencing and bioinformatic analysis of genetic data. We confirm that the services were performed properly and on time. We recommend Intelliseq as a reliable contractor.

Analityk Genetyka
We have been using the IntelliseqFlow platform from the very beginning - we’ve also participated in the beta-tests. The app facilitated the diagnosis of genetic diseases related to the neuromuscular system. We are convinced that the application fulfills its role 100%, enabling very fast and accurate analyses of exome and genome samples, in various areas of interest.

Mossakowski Medical Research Centre Polish Academy Of Sciences
Intelliseq performed for us the sequencing of the full transcriptome of RNA samples and bioinformatics analysis of the obtained data. I confirm that the service was performed properly and on time. I recommend Intelliseq as a reliable contractor.

Jagiellonian University Medical College
We’ve tested the IntelliseqFlow platform and are impressed with its functionality and simplicity of use. It enables users to transfer raw DNA data into full reports with clinical insights with no bioinformatics skills needed. We recommend using the IntelliseqFlow platform especially for entities that want to quickly access genome-based diagnostics market and precision medicine with full cost control.

ixLayer a complete solution for Health Testing
We use the IntelliseqFlow platform for the RNA-seq analyses within our research projects in the Department of Molecular Neuropharmacology. The analyses were carried out quickly and accurately without any problems. IntelliseqFlow met all our expectations and we are happy to recommend it.

Maj Institute of Pharmacology Polish Academy Of Sciences

Place in workflow IntelliseqFlow works for labs as a cloud-based platform with no installation required or as a plug-in for laboratory information management system (LIMS).

Features IntelliseqFlow accelerates and simplifies NGS data analysis and interpretation due to its versatility.

Automatic and scalable one platform, any NGS analysis

Cost-effective No upfront cost and fixed price per analysis

Flexible easy integration with LIMS, custom installations, white-label

Complete From raw sequence to clinical insight reports

Intuitive Simple to use, designed by practitioners for practitioners

Comprehensive 100+ Workflows available, from simple to complex ones

Bioinformaticianless User-friendly interface - easy to operate

SaaS Software as a service platform with no installation required

Fast Few steps and a bit of time from data to result

Secure ISO:13485 and HIPAA

How can we help you?

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

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:

NGS data analysis,
Bioinformatics and software engineering,
High-throughput sequencing.

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

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

NGS pipeline development in cooperation with SCC Soft Computers Implementation of the NGS data processing workflow for genome sequencing data Read more
Partnership with Helix MyTraits Sport mobile app for genetic analysis of athletic ability and obesity risk Read more
Collaboration with ixLayer for Vitalleo Developing together a customized genetic test Read more
Transcriptomic research collaboration with BioMed X Institute Analysis and interpretation of RNAseq data-set profiling gene expression alterations in the brain Read more
Cooperation with Adamed during MIT Enterprise Forum CEE acceleration program Pharmacogenetic test prototype based on whole genome sequencing Read more
Collaboration with Boehringer Ingelheim Project dedicated to central nervous system diseases Read more

Our most recent blog articles Follow us and read our posts to learn more.

Structural Variants (SVs) – Large-scale genome rearrangements

The Structural Variants (SVs) are large-scale genetic alterations that affect the structure of th ...

GRCh38: The golden standard in human genome assembly

A reference genome is a representation of a specific organism’s genetic material. It serves ...

Genome alignment tools: BWA-MEM or DRAGMAP?

Alignment involves the step when the short fragments of DNA sequence are being matched to the ref ...