Genomics

Genome Sequencing

Genomic sequencing services provide whole genome sequencing (Whole Genome Sequencing, WGS) and related genomics research solutions, suitable for genetic information analysis of human, plant and animal, microbial, and complex population samples. We use next-generation sequencing (NGS) and third-generation sequencing (TGS) technologies, supporting short-read (Illumina), long-read (PacBio, Nanopore), and hybrid assembly strategies to ensure high accuracy and coverage in genome sequencing.

Whole-genome de novo sequencing
Used for genome assembly and evolutionary studies of new species
Resequencing
Used for SNP, Indel, structural variation (SV), and copy number variation (CNV) analysis
Metatranscriptome
Metagenomic and metatranscriptomic sequencing for single bacteria or environmental microbiomes supports 16S/ITS and other related studies
Whole-genome methylation sequencing
Analyzes DNA methylation modifications to study epigenetic regulation
Single-cell genome sequencing
Used for genome assembly and evolutionary studies of new species

Our genomic sequencing services are widely applied in genetic research, population evolution analysis, disease association studies, biodiversity, and precision medicine, providing high-quality genomic data support for scientific research and clinical studies.