Next Generation Sequencing
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GenNext is a product of Geniva.
For more information about Geniva, visit our website: geniva.bio
GENNEXT Platform
GenNext is a network infrastructure specifically developed for the analysis of health big data. GenNext’s uniquely designed architecture allows each device on the network to transmit data directly to other devices. In this way, data can be shared and analyzed without the need to save, archive, and process personal data in a central location.
Due to GenNext's uniquely designed network architecture, personal data is not recorded and stored.
GenNext protects you against all possible data breaches within the scope of KVKK-TR and EU-GDPR with its decentralized, peer-to-peer (P2P) structure.
Why GenNext?
Fully automated data processing, analysis and reporting
Fast, efficient and secure data analysis without delays in data loading and analysis
Exceptional user experience with low cost and high quality
Services
GenNextwellness
June 2024
GenNextklinik
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.
With GenNextklinik, you can perform data processing, annotation, and variant filtering starting from a FASTQ, BAM, or VCF file, and form a report with the selected variant(s) using our automatic reporting tool.
Due to GenNextklinik‘s streamlined user-friendly interface, you can save the options you use most frequently in your analysis for the next time. You can view your saved analysis and filtering options and customize them as you wish.
The platform offers duo and trio case filtering options in addition to both predefined and customizable filtering options -including clinical, research, and specialized- to facilitate your analyses. GenNextklinik offers over 150 up-to-date annotators, HPO (Human Phenotype Ontology)-integrated gene listing options that can be saved within your account. It also offers a CNV filtering tool to perform case-specific analysis for your clinical, research, and challenging cases suitable for routine diagnostics.
GenNextklinik is suitable for the analysis of both germline and somatic variants. Due to the integrated system of the platform, the variant can be visualized and validated using the BAM file simultaneously during the variant filtering step, and if necessary, it can be displayed and analyzed together with RNA sequencing data.
GenNextklinik can be run – depending on the size of your data:
- on your own computer or corporate servers
- on GenNext Computation Units
- with GenNext Cloud using our cloud service.
With GenNextklinik
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