iGeneTech Bioscience Co., Ltd.
EN
Blogs

Blogs

07
11, 2025
The Turnaround Time for Whole Exome Testing can be completed within 12 hours!
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 ...
05
11, 2025
iGeneTech has innovatively launched the OmniTrait Methylation Panel
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...
03
11, 2025
iGeneTech Whole-Genome Capture Technology: A New Tool for Pathogen Monitoring
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...
31
10, 2025
How iGeneTech Conducts the Application of MRD Detection
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 ...
30
10, 2025
iGeneTech Helped Its Client(s) Publish Research Findings in Journal of Genetics: NGS Technology Identifies Novel DMD Gene Duplication Variants
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...
27
10, 2025
New Product Launch-RNA Exome: Comprehensive and Accurate Capture of Whole Transcriptome Information
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 ...
20
10, 2025
iGeneTech New Product Launch: Human Genotyping Product Covering 630,000 SNP Loci
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...
13
10, 2025
Bioinformatics Mini-Course: Plot GC Content - Sequencing Depth Distribution in 3 Steps
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...
30
09, 2025
How does iGeneTech improve the uniformity of the panel?
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...
28
09, 2025
Protect the next generation, starting with carrier screening
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 ...