In the Neonatal Intensive Care Unit (NICU), clinicians face highly challenging cases every day. These infants often develop severe symptoms shortly after birth, such as respiratory failure, metabolic ...
Methylation, as the core modification in epigenetics, directly regulates gene expression and chromatin structure. Its abnormal patterns serve as early biomarkers for cancer, neurodegenerative diseases...
In the work of infectious disease prevention and control as well as emergency monitoring, the accurate identification and genotyping analysis of pathogens are key to achieving scientific prevention an...
01 Proven and Effective Detection SolutionCurrently, among domestic and international detection solutions, after multiple comparisons and validations of clinical data between the fixed-panel approach ...
Duchenne Muscular Dystrophy (DMD) and Becker Muscular Dystrophy (BMD) are X-linked recessive monogenic disorders caused by mutations in the DMD gene. They primarily affect males, who present with prog...
iGeneTech RNA Exome is a capture product targeting the human whole transcriptome. Designed based on the RefGene and RefSeq databases, it enables targeted capture of a 46.1 Mb region, including coding ...
As a genotyping tool specifically designed for East and Southeast Asian populations, the traditional solid-phase microarray has long served as a commonly used variant detection tool, relying on over 6...
What Exactly Is a "GC Content - Sequencing Depth" Heatmap? How to Interpret It? And How to Plot It?1. In genomic sequencing data analysis, "whether GC content affects sequencing depth&q...
Gene Capture Uniformity IndicatorsiGeneTech has been deeply engaged in the gene capture industry for 11 years. It has always adhered to taking clinical needs as the core and built full-chain service c...
Do You Know?On average, each person carries 2–3 recessive pathogenic genetic variants. They may show no symptoms themselves, but if both partners in a couple carry the same gene mutation, their baby ...