Analityk Group

Are you facing complex genetic analysis challenges in microbiology or virology?
Do you require microbiological diagnostics with CE-IVD certification?
Is there a need to expand your virological diagnostic capabilities?

Arrow Diagnostics offers simple and effective solutions to meet these demands.

Arrow Diagnostics is a manufacturer of targeted NGS-based panels compatible with Illumina sequencing platforms. Established in 2003, the company specializes in the development of high-quality reagents and diagnostic kits for molecular biology, microbiology, and virology.

Learn more about our full product portfolio: https://arrowdiagnostics.it/en/home/

For inquiries or further information, please contact us: https://www.analitykgenetyka.pl/kontakt

Funding for the G4PL – Genomics for Poland project!

We are pleased to announce that the project entitled G4PL – Genomics for Poland, headed by Prof. Luiza Handschuh, has received funding from the European Funds for a Smart Economy (FENG) program, Action 2.4 Research Infrastructure of Modern Economy.

The consortium leader, the Institute of Bioorganic Chemistry PAS along with the Poznan Supercomputing and Networking Center, will collaborate with eleven research units:
• Institute of Human Genetics PAS
• Nencki Institute of Experimental Biology PAS
• Poznan University of Technology
• University of Warsaw
• Medical University of Bialystok
• University of Lodz
• University of Gdansk
• Jagiellonian University
• Cardinal Stefan Wyszynski National Institute of Cardiology – National Research
Institute in Warsaw
• Maria Sklodowska-Curie National Research Institute of Oncology – Gliwice Branch
• Łukasiewicz Research Network – Polish Center for Technology Development

The primary objective of the project is to establish a nationwide network of laboratories conducting research and providing services in the field of genomics, serving academic, commercial and healthcare institutions. These activities will support the development of science, personalized medicine, precise diagnostics, innovative therapies, and targeted prevention.

The network will be equipped with advanced infrastructure for genome research, including high-throughput long-read sequencing machines and a device for creating optical maps. The project will also result in the collection of new genomes, including those from patients with rare diseases, the integration and re-analysis of existing data, and their sharing within a nationwide repository. New IT tools for genome analysis will also be developed, utilizing artificial intelligence algorithms and quantum technologies.

Population genomic research contributes to a deeper understanding of genetic variation, disease prevalence, and predisposition, enabling improved diagnostics, personalized treatment, and more effective preventive measures. It also translates into tangible economic benefits, as well-targeted prevention, precise diagnostics, and personalized therapy reduce healthcare costs. The project plans to sequence samples from 6,000-7,000 donors. Some of these samples will constitute Poland's contribution to the Genome of Europe (GoE) project.

Project value: PLN 248,337,770.24.
Project funding: PLN 180,481,656.59.
Implementation period: 2026-2029.
The non-financial contribution to the project is made by BCODERS S.A. and Analityk Genetyka Unrug Wójtowicz Sp. k.

The project is co-financed by the European Union under the European Funds for a Smart Economy program.

Webinar: New AI Strategies in Rare Disease Diagnostics

Join us for an upcoming webinar, held in collaboration with the NHS North West Genomic Laboratory Hub (NWGLH), where experts will explore how DRAGEN, Emedgene, and Illumina Genomic AI are transforming the analysis and interpretation of genetic variants in clinical trials.

Agenda highlights:

Strategies for implementing AI-powered software within NWGLH and its impact on NHS services

Demonstration of the high accuracy and efficiency in analyzing and interpreting various genetic variants, including:
SNV, indel, CNV, SV, STR, and mtDNA

Aligning AI-assisted interpretation with established best practices

Register here:

Warsaw Single Cell and Spatial Discovery Symposium 2025

We are pleased to invite you to the upcoming Warsaw Single Cell and Spatial Discovery Symposium, taking place on October 8 at the Center for Biological and Chemical Sciences, University of Warsaw (101 Żwirki i Wigury Street).

This event is designed for both newcomers beginning their journey with single-cell and spatial technologies, as well as for experienced users of 10x Genomics platforms.

As in previous years, the symposium will feature engaging presentations from researchers who apply these cutting-edge technologies in their work. It also offers a valuable opportunity to network, collaborate, and share experiences with fellow participants.

Register today!

10x Genomics The Single Cell and Spatial Discovery Symposium is a unique event intended for those new to single cell and spatial technology as well as seasoned 10x Genomics technology users. The highly informative series of exclusive scientific sessions will feature keynote presentations by leading researchers a...