Whole Genome Sequencing
Decode entire genomes to uncover genetic variations, enabling comprehensive insights into organisms or diseases
Whole Transcriptome Sequencing
Analyze RNA expression profiles to study gene activity and regulatory mechanisms across various conditions
Metagenome (16s/18s/ITS)
Explore the genetic composition of microbial communities to understand their roles in health, environment, and industry
Genotyping by Sequencing (GBS)
Identify genetic markers efficiently for applications in breeding, population genetics, and association studies
Bisulfite Sequencing
Detect DNA methylation patterns to study epigenetic modifications and their role in gene regulation
ATAC Sequencing
Map chromatin accessibility to identify regulatory regions influencing gene expression and cellular function
Single Cell Sequencing
Investigate the genetic heterogeneity of individual cells to reveal unique insights into cellular functions and diseases
SNP/SSR Analysis
Detect simple sequence repeats (SSRs) and single nucleotide polymorphisms (SNPs) for genetic diversity and trait mapping
Whole Exome Sequencing
Focus on protein-coding regions to identify disease-causing mutations with high precision and efficiency
Epigenome Sequencing
Uncover DNA methylation and histone modification patterns to study gene regulation and epigenetic changes linked to development and disease