Microarray
Our Microarray analysis services provide a wide-ranging toolkit for investigating genetic information, including Transcriptomics, Genomics, and Epigenetics Microarray Services.
- Within Epigenetics Microarray, we offer ChIP-on-chip and DNA Methylation Microarray Service.
- Our Genomics Microarray Service includes CGH and SNP Microarray Service.
- In Transcriptomics Microarray, we cover LncRNA Microarray, MicroRNA, and Gene Expression Profiling Microarray Services.
Sequencing
We provide three types of sequencing methods: Human Whole Genome Sequencing, Whole Exome Sequencing and Transcriptome Sequencing.
- Human whole genome sequencing (hWGS) deciphers complete genetic compositions, identifying vital genomic variations like SNPs, InDels, SVs, and CNVs cost-effectively.
- Whole Exome sequencing (WES) uses Next Generation Sequencing (NGS) to offer a budget-friendly alternative to whole genome sequencing, allowing in-depth analysis of genome variants, germline and somatic mutations, and pathogenic mechanisms.
- Transcriptome Sequencing services cover mRNA and non-coding RNA, including popular long non-coding RNA, small RNA, and circular RNA sequencing. We also provide whole transcriptome sequencing to explore interactions between coding and non-coding RNAs in eukaryotes.
Genotyping
We offer comprehensive Whole-Genome SNP Genotyping, utilizing microarray technology and high-throughput Next Generation Sequencing (NGS). This approach enables wide-ranging exploration of the entire genome, allowing for the detection and screening of SNP loci. These SNP markers support genome-wide association studies, which help identify genetic variations associated with complex disorders.
Bioinformatics
Himagene offers two types of Bioinformatic services: Genomic Data Analysis and Transcriptomatic Data Analysis.
- Genome Data Analysis is the study of genetic information within an organism’s genome. It involves identifying genes, regulatory elements, and genetic variations. This analysis also explores genetic relationships within populations and individuals.
- Transcriptomic Data Analysis focuses on characterizing all transcriptional activity, including coding and non-coding RNA transcripts in a sample. This analysis identifies candidate genes and markers associated with specific traits
Genetic Consulting
Our genetic counselors evaluate the risk of inherited conditions, including birth defects. They discuss genetic test results with individuals and families, aiding them in decision-making based on these results. Additionally, they provide information to other healthcare providers.
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