{"id":13842,"date":"2025-03-19T18:40:36","date_gmt":"2025-03-19T15:40:36","guid":{"rendered":"https:\/\/gennext.bio\/?page_id=13842"},"modified":"2026-02-04T12:06:05","modified_gmt":"2026-02-04T09:06:05","slug":"gennext-clinical","status":"publish","type":"page","link":"https:\/\/gennext.bio\/en\/gennext-clinical\/","title":{"rendered":"Gennext Clinical"},"content":{"rendered":"
[vc_section full_width=”stretch_row” pix_over_visibility=”” t_flip_h=”true” responsive_css=”{“pix_res_sm_pt“:“20“,“pix_res_sm_pb“:“20“,“pix_res_md_pt“:“40“,“pix_res_md_pb“:“40“}” css=”.vc_custom_1764692808092{padding-top: 10px !important;padding-bottom: 20px !important;}” t_custom_height=”200px”][vc_row full_width=”stretch_row” content_placement=”middle” pix_particles_check=”” responsive_css=”{“pix_res_sm_pt“:“40“,“pix_res_sm_pb“:“40“,“pix_res_md_pt“:“40“,“pix_res_md_pb“:“40“}”][vc_column width=”1\/2″ css=”.vc_custom_1604715604745{padding-top: 20px !important;padding-bottom: 20px !important;}”]Clinical Genomics Platform<\/span><\/span><\/span>

In Clinical Genetic Analyses, <\/span><\/span>Powerful, Fast and Reliable <\/span><\/span>Solution.<\/span><\/span><\/h2><\/div>

\r\nGennext Clinic is a clinical decision support platform that accelerates high-accuracy genetic analysis, phenotype matching, and interpretation processes for rare and inherited diseases.\r\n<\/p><\/div><\/svg>Become a Clinical Partner<\/span><\/a>[\/vc_column][vc_column width=”1\/2″ content_align=”text-center”]

\"Image<\/div><\/div>[\/vc_column][\/vc_row][\/vc_section][vc_section full_width=”stretch_row” pix_over_visibility=”” css=”.vc_custom_1764692801555{padding-bottom: 20px !important;background-color: #f8f9fa !important;}”][vc_row content_placement=”middle” pix_particles_check=”” css=”.vc_custom_1592058675604{padding-bottom: 20px !important;}” el_class=”mx-100″][vc_column width=”1\/2″ css=”.vc_custom_1591311397311{padding-right: 30px !important;padding-bottom: 30px !important;padding-left: 30px !important;}”]

We <\/span><\/span> transform <\/span><\/span> complex <\/span><\/span> genetic <\/span><\/span> data <\/span><\/span> into <\/span><\/span> meaningful <\/span><\/span> insights. <\/span><\/span> <\/h4><\/div>
<\/path><\/g><\/svg><\/div>Medical Genetics Specialists<\/span><\/div>
<\/path><\/g><\/svg><\/div>Pediatric Geneticists<\/span><\/div>
<\/path><\/g><\/svg><\/div>Pathologists and Oncologists<\/span><\/div>
<\/path><\/g><\/svg><\/div>University Hospitals<\/span><\/div>
<\/path><\/g><\/svg><\/div>Private Hospitals<\/span><\/div>
<\/path><\/g><\/svg><\/div>Clinical Laboratories<\/span><\/div><\/div><\/div><\/div><\/div>[\/vc_column][vc_column width=”1\/2″]
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Accelerates time-consuming analysis workflows in clinical settings<\/h5>
\r\nReduces variant analysis and interpretation timelines from weeks to days.\r\n<\/div><\/div><\/div>
<\/g><\/svg><\/div>
GPU-accelerated variant analysis infrastructure<\/h5>
\r\nDelivers high accuracy and reproducibility with GATK\/DRAGEN-compatible pipelines.\r\n<\/div><\/div><\/div>
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Secure data processing compliant with data protection regulations<\/h5>
\r\nThanks to a federated data model, sequencing data never leaves the institution.\r\n<\/div><\/div><\/div><\/div><\/div>[\/vc_column][\/vc_row][\/vc_section][vc_section full_width=”stretch_row” pix_over_visibility=”” css=”.vc_custom_1764692780021{padding-top: 10px !important;padding-bottom: 10px !important;background-color: #f8f9fa !important;}”][vc_row full_width=”stretch_row” pix_particles_check=”” css=”.vc_custom_1764679371694{padding-bottom: 5px !important;}”][vc_column]

Clinical <\/span><\/span> Use <\/span><\/span> Cases <\/span><\/span> <\/h3><\/div><\/div>[\/vc_column][\/vc_row][vc_row full_width=”stretch_row” equal_height=”yes” content_placement=”middle” pix_particles_check=”” css=”.vc_custom_1764678568255{padding-bottom: 0px !important;}”][vc_column]
Rare \/ Inherited<\/span><\/a><\/div>
Oncology<\/span><\/a><\/div><\/div>
[vc_row_inner][vc_column_inner width=”2\/3″ css=”.vc_custom_1764781680585{padding-right: 20px !important;padding-left: 20px !important;background-color: #FFFFFF !important;border-radius: 5px !important;}”]
Rare \/ Inherited Diseases<\/h5><\/div>

\r\nAdvanced modules that simplify the analysis of genetically driven disorders in pediatric and adult patients.\r\n<\/span><\/p><\/div><\/div>

<\/path><\/g><\/svg><\/div>HPO (Human Phenotype Ontology)-supported variant prioritization<\/span><\/div>
<\/path><\/g><\/svg><\/div>Pathogenicity classification according to ACMG (American College of Medical Genetics and Genomics) and AMP (Association for Molecular Pathology) standards<\/span><\/div>
<\/path><\/g><\/svg><\/div>Trio and segregation analysis<\/span><\/div>
<\/path><\/g><\/svg><\/div>University Hospitals<\/span><\/div>
<\/path><\/g><\/svg><\/div>CNV \/ SNV \/ Indel detection<\/span><\/div>
<\/path><\/g><\/svg><\/div>Clinically compliant PDF\/JSON reports<\/span><\/div><\/div><\/div>[\/vc_column_inner][vc_column_inner width=”1\/3″ css=”.vc_custom_1764781668654{padding-right: 20px !important;padding-left: 20px !important;background-color: #FFFFFF !important;border-radius: 5px !important;}”]
Sample Report<\/h5><\/div>
\"Image<\/div><\/div><\/svg>Sample Report<\/span><\/a>[\/vc_column_inner][\/vc_row_inner]<\/div>
[vc_row_inner][vc_column_inner width=”2\/3″ css=”.vc_custom_1764678775855{padding-right: 20px !important;padding-left: 20px !important;background-color: #FFFFFF !important;}”]
Oncology<\/h5><\/div>

\r\nAnalyses that support treatment decisions through tumor profiling and actionable gene sets.\r\n<\/span><\/p><\/div><\/div>

<\/path><\/g><\/svg><\/div>Tumor mutation profiling<\/span><\/div>
<\/path><\/g><\/svg><\/div>Actionable variant detection<\/span><\/div>
<\/path><\/g><\/svg><\/div>FDA, ESMO, NCCN compliant<\/span><\/div>
<\/path><\/g><\/svg><\/div>TMB, MSI and HRD calculations supported<\/span><\/div>
<\/path><\/g><\/svg><\/div>Clinical decision support report (PDF\/JSON)<\/span><\/div>
<\/path><\/g><\/svg><\/div>Clinically compliant PDF\/JSON reports<\/span><\/div><\/div><\/div>[\/vc_column_inner][vc_column_inner width=”1\/3″ css=”.vc_custom_1764678821967{padding-right: 20px !important;padding-left: 20px !important;background-color: #FFFFFF !important;}”]
Sample Report<\/h5><\/div>
\"Image<\/div><\/div><\/svg>Sample Report<\/span><\/a>[\/vc_column_inner][\/vc_row_inner]<\/div><\/div><\/div><\/div><\/div>[\/vc_column][\/vc_row][\/vc_section][vc_section full_width=”stretch_row” pix_over_visibility=”” css=”.vc_custom_1764681767560{padding-top: 10px !important;padding-bottom: 10px !important;background-color: #ffffff !important;border-radius: 10px !important;}”][vc_row gap=”25″ equal_height=”yes” content_placement=”middle” pix_particles_check=”” css=”.vc_custom_1587871299654{border-radius: 10px !important;}”][vc_column content_align=”text-center”]

How <\/span><\/span> It <\/span><\/span> Works? <\/span><\/span> <\/h2><\/div>[\/vc_column][\/vc_row][vc_row pix_particles_check=”” css=”.vc_custom_1588778312964{padding-right: 30px !important;padding-left: 30px !important;}”][vc_column width=”1\/4″]
\"Data<\/div>
Data Ingestion<\/h6>
\r\nFASTQ\/BAM\/VCF import, S3\/SFTP connections, and on-premise deployment options.\r\n<\/div><\/div><\/a><\/div><\/div>[\/vc_column][vc_column width=”1\/4″]
\"Analysis<\/div>
Analysis Workflow<\/h6>
\r\nGATK-compliant and reproducible genomic analysis pipelines with integrated QC processes.\r\n<\/div><\/div><\/a><\/div><\/div>[\/vc_column][vc_column width=”1\/4″]
\"Interpretation\"<\/div>
Interpretation<\/h6>
\r\nACMG guidelines, phenotype matching, literature review, and evidence grading.\r\n<\/div><\/div><\/a><\/div><\/div>[\/vc_column][vc_column width=”1\/4″]
\"Reporting\"<\/div>
Reporting<\/h6>
\r\nWhite-label PDF\/JSON outputs with full integration into clinical workflows via LIMS\/EHR systems.\r\n<\/div><\/div><\/a><\/div><\/div>[\/vc_column][\/vc_row][\/vc_section][vc_section full_width=”stretch_row” pix_over_visibility=”” css=”.vc_custom_1764682333424{padding-top: 10px !important;padding-bottom: 30px !important;background-color: #ffffff !important;border-radius: 10px !important;}”][vc_row gap=”25″ equal_height=”yes” content_placement=”middle” pix_particles_check=”” css=”.vc_custom_1587871299654{border-radius: 10px !important;}”][vc_column content_align=”text-center”]

Validation <\/span><\/span> & <\/span><\/span> Evidence <\/span><\/span> <\/h2><\/div>[\/vc_column][\/vc_row][vc_row pix_particles_check=”” css=”.vc_custom_1588778312964{padding-right: 30px !important;padding-left: 30px !important;}”][vc_column width=”1\/2″]
\"Validation\"<\/div>
Validation<\/h6>
\r\nWet-lab and in-silico validation sets; sensitivity, specificity, and accuracy metrics.\r\n<\/div><\/div><\/a><\/div><\/div>[\/vc_column][vc_column width=”1\/2″]
\"Scientific<\/div>
Scientific Evidence<\/h6>
\r\nCurated literature, up-to-date database versions, and review audit trails.\r\n<\/div><\/div><\/a><\/div><\/div>[\/vc_column][\/vc_row][\/vc_section][vc_section full_width=”stretch_row” pix_over_visibility=”” css=”.vc_custom_1764682333424{padding-top: 10px !important;padding-bottom: 30px !important;background-color: #ffffff !important;border-radius: 10px !important;}”][vc_row gap=”25″ equal_height=”yes” content_placement=”middle” pix_particles_check=”” css=”.vc_custom_1587871299654{border-radius: 10px !important;}”][vc_column content_align=”text-center”]

Data <\/span><\/span> Security <\/span><\/span> <\/h2><\/div>[\/vc_column][\/vc_row][vc_row pix_particles_check=”” css=”.vc_custom_1588778312964{padding-right: 30px !important;padding-left: 30px !important;}”][vc_column width=”1\/3″]
\"GPU-based<\/div>
GPU-based analysis architecture<\/h6>
\r\nAn optimized infrastructure that processes large-scale genomic data within minutes.\r\n<\/div><\/div><\/a><\/div><\/div>[\/vc_column][vc_column width=”1\/3″]
\"Federated<\/div>
Federated data sharing<\/h6>
\r\nData remains on-premise; analysis is performed within Gennext\u2019s isolated and secure environment.\r\n<\/div><\/div><\/a><\/div><\/div>[\/vc_column][vc_column width=”1\/3″]
\"KVKK-compliant<\/div>
KVKK-compliant system<\/h6>
\r\nAll processes are executed on an end-to-end encrypted infrastructure.\r\n<\/div><\/div><\/a><\/div><\/div>[\/vc_column][\/vc_row][\/vc_section][vc_row full_width=”stretch_row” pix_particles_check=”” css=”.vc_custom_1593136293430{padding-top: 80px !important;padding-bottom: 80px !important;}”][vc_column offset=”vc_col-lg-offset-2 vc_col-lg-8″]
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