Whole Genome Sequencing (WGS)
Our WGS service provides unparalleled coverage of the entire
genome, allowing for comprehensive analysis of genetic variations,
structural variations, and functional elements across the genome.
With state-of-the-art sequencing technology, we ensure
high-quality data output, enabling researchers to uncover novel
insights into genetic mechanisms underlying diseases and traits.
Whole Exome Sequencing (WES)
Targeting the exome, our WES service focuses on sequencing the
protein-coding regions of the genome, providing a cost-effective approach
to explore the functional elements most relevant to disease and phenotype.
By capturing key coding regions, researchers can identify rare variants,
mutations, and potential disease-causing genes with high precision,
facilitating in-depth analysis and discovery in genetic research.
Transcriptome Sequencing
Our transcriptome sequencing service offers a comprehensive analysis
of gene expression patterns, providing valuable insights into the dynamic
regulation of gene expression in various biological processes and disease
states. By profiling the transcriptome, researchers can uncover key
regulatory mechanisms, identify novel transcripts, and elucidate the
underlying molecular pathways involved in disease pathogenesis.
Run-only Sequencing
For clients who have already prepared their sequencing
libraries, our run-only sequencing service offers efficient
and cost-effective sequencing solutions. With flexible
options for sequencing platforms and throughput, we deliver
high-quality sequencing data with rapid turnaround times,
allowing researchers to focus on data analysis and
interpretation without the hassle of library preparation.
