How do we classify variants according to the ACMG/AMP criteria?
Variant classification is crucial for the clinical interpretation of findings in patients’ genetic makeup. Intelliseq’s reports
May 12, 2021
email: contact@intelliseq.com
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Bioinformatic products. Bioinformatics services. R&D.
DNA analysis made simple
bioinformatic tools for genome-based medicine
Sign up now to get early access to IntelliseqFlow!
IntelliseqFlow
Software as a service platform for NGS data analysis with no upfront cost. IntelliseqFlow translates your raw DNA data into complete reports with clinical insights.
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.
Sign up now to get early access to IntelliseqFlow!
Automatic and scalable
one platform, any NGS analysis
Complete
from raw sequence to clinical insight reports
Bioinformaticianless
user-friendly interface - easy to operate
Cost-effective
no upfront cost and fixed price per analysis
SaaS
software as a service platform with no installation required
Secure
ISO:13485 and HIPAA
Flexible
easy integration with LIMS, custom installations, white-label
Comprehensive
100+ Workflows available, from simple to complex ones
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.
Our Partners
Learn more about our partners and the use cases from our collaboration.
Our Blog
Interview for the DNAweekly
How did Intelliseq start? What capabilities does IntelliseqFlow platform bring into the lab? How do we
February 22, 2021
User-friendly and accessible DNA test reports
Well-designed reports showing DNA test results facilitate the work of genetic consultants and help customers understand
July 30, 2020
Polygenic risk score application including severe COVID-19
The vast majority of differences between humans is caused by variations in their DNA, usually by
July 15, 2020
System for pharmacological interpretation of the human genome
Pharmacogenomics, according to the National Library of Medicine, is the study of how genes affect a
June 26, 2020
Expanding our R&D potential
We have co-authored 4 new papers as a result of a cooperation with multiple research institutes:
June 5, 2020
Genomics at scale – building reproducible, scalable workflows for genome-based medicine
Contemporary computational genomics is inseparable from all the technical hurdles that arise when there is a
May 6, 2020
We’re ISO 13485 certified!
We can proudly announce that our company has successfully passed the audit for the ISO 13485:2016
May 5, 2020
Intelliseq recognized by FDA
In October 2019, we participated in the BioCompute Object (BCO) App-a-thon organized by PrecisionFDA partnered with
April 5, 2020