GenetureSeq Prep Kit - Hi-Exon 35 Panel

Genomic sequencing panel for cancer-related mutation and biomarker detection. Supports precision oncology treatment planning and selection.

Sequencing panel for identifying genetic variations associated with hereditary and congenital disorders. Enables comprehensive genetic disease diagnosis.

A comprehensive genetic testing panel designed for detecting genetic variations associated with hereditary diseases and health conditions. The panel utilizes advanced sequencing technology for precise variant identification.

Comprehensive PCR-based screening panel for multiple genetic diseases. Allows simultaneous detection of multiple genetic markers in single analysis.

Collection of pre-configured next-generation sequencing panels available for immediate clinical use. Enables rapid deployment of validated genomic testing workflows for common applications in oncology, constitutional genetics, and precision medicine.

Comprehensive multigene panel for hereditary disease identification and cancer risk assessment. Provides clinical-grade analysis with detailed genomic reporting.

A research use only whole exome sequencing panel for comprehensive genomic analysis. Enables detection of variants across coding regions of the genome. Designed for translational research and exploratory genomic studies.

A research use only targeted sequencing panel for comprehensive genomic analysis. Provides high-accuracy genomic data through targeted region sequencing. Designed for translational research applications.

Kit for preparation of next-generation sequencing libraries covering the entire human exome and mitochondrial genome. Designed for comprehensive genomic analysis applications requiring high-throughput sequencing capabilities.

A semi-automated kit for next-generation sequencing (NGS) of the exonic regions of the human genome, covering a 37.64 Mb region using genomic DNA extracted from whole blood and buccal swabs. The kit includes reagents for the preparation of DNA libraries enriched in exonic regions, intended for use on Illumina NGS sequencing platforms. It is designed for the identification of genetic variants in the exome to support the diagnosis of hereditary diseases, detect variants related to disease predisposition, and guide personalized medicine.

Next-generation sequencing testing kit for comprehensive genomic analysis and variant detection. Enables high-throughput sequencing for applications in molecular diagnostics and research.

iGenetech NGS kits enable next-generation sequencing for genomic analysis and molecular diagnostics. These kits support clinical applications including genetic testing, disease screening, and precision medicine workflows. Complete reagent systems designed for laboratory-based sequencing platforms.