GenNext is a decentralized peer-to-peer (P2P) genomic data analysis platform. Due to the design and structure of GenNext, genomic data is not shared with anyone other than the computer where the analysis will be performed and the person performing the analysis.

GenNext is differentiated from other data analysis platforms on the market thanks to its unique architecture and network structure, providing an exceptional user experience.

Successful data analysis and reporting: The GenNext platform incorporates the latest literature in genetics/genomics, enabling successful analysis of next-generation sequencing data.

Privacy and security: With GenNext, data is not stored and saved in a centralized location, which means there is less risk of your data being compromised by malicious actors.

High-throughput and fast data transfer: Thanks to GenNext’s specially developed network structure, data is transferred directly between users. This significantly reduces the time and bandwidth required to transfer data to centralized servers or cloud platforms used in traditional big data analysis platforms.

Secure analysis of personal data and EU-GDPR compliance: In a decentralized P2P network, data is stored and analyzed locally on users’ devices. This provides greater privacy and security compared to traditional big data analytics platforms that depend on storing and processing data in a central location. In addition, this structure allows data to be analyzed in compliance with EU-GDPR (The European General Data Protection Regulation) and KVKK (Personal Data Protection Law-Turkiye).

Alignment with Web3.0 principles: Decentralized P2P networks are one of the underlying technologies of Web3.0, which can be defined as a decentralized and user-owned internet. GenNext’s network design, which enables decentralized P2P data transfer and analysis, is in line with the principles underlying Web3.0.

GenNextklinik is a genomic data analysis and reporting tool within the GenNext platform. With its rich analysis and annotation tools, advanced filtering and reporting options, and user-friendly interface, GenNextklinik offers a unique genomic data analysis experience.

Comprehensive analyses and streamlined diagnostic process: GenNextklinik aims to accurately detect and prioritize genomic variants thanks to its comprehensive workflow and rich annotation options developed by following the current literature and based on Best-Practice applications. This makes it a powerful aid in the diagnosis of genetic diseases. Using the pre-customized filtering options integrated into the platform, the clinically important variants among thousands are prioritized with GenNextklinik ,which helps accelerate the diagnostic process. In addition, thanks to the multi-sample analysis options, the genetic disease diagnosis process is supported by taking heredity into account with Duo and Trio analyzes.

Find actionable variants and treatment options in cancer: GenNextklinik uses a comprehensive somatic variant detection workflow and helps identify genetic alterations that can support the diagnostic-treatment process. Using up-to-date literature and databases, identified variants are reported and presented in terms of their diagnostic significance, pathogenicity and drug interactions that can help the therapeutic process.

Fast reporting: With GenNextklinik‘s automated report generation feature, you can report on the variants you select after analysis using report templates and print the report format instantly. You can also upload the report format you want to use to the platform and access variant reports in the format you specify in seconds.