Solution reagent kit NEXome Mini Panel v1.0

for researchclinicalgenetic

NEXome Mini Panel focuses on the exome associated with clinical inherited diseases, with probe coverage spanning a 16.1 Mb genomic region involving 5650 clinically significant genes and encompassing over 4000 genetic disorders. In comparison to the whole exome panel, the NEXome Mini Panel can be used to rapidly and efficiently detect pathogenic genetic variations within target genes in the human genome. This not only reduces sequencing costs but also significantly shortens data analysis time. Feature Highly Targeted: Focuses on the exome associated with clinical inherited diseases, covering a 16.1 Mb genomic region, involving 5650 genes related to over 4000 clinical genetic disorders. High Accuracy: Based on the probe hybridization capture principle, it can accurately detect genetic variations within target genes, providing reliable data support for subsequent research. High Efficiency: Compared to the whole exome Panel, the NEXome Mini Panel can rapidly detect pathogenic genetic variations within target genes, thereby reducing data analysis time and minimizing turnaround time. Cost-effective: Aim to only include clinically significant regions specifically related to inherited diseases, effectively reducing sequencing costs.