Sequencing Solutions
Unlocking Life’s Blueprint with Precision and Purpose
At GeneInsight, we empower researchers, institutions, and innovators to explore the full potential of genomics. Our advanced sequencing solutions are designed to reveal the intricate layers of biology—from genome structure to gene expression—enabling discoveries across fields such as personalized medicine, agriculture, biodiversity, and environmental science.
Our platform combines state-of-the-art sequencing technologies with AI-enhanced data interpretation to deliver high-resolution insights with unmatched speed and accuracy. Whether you’re decoding plant genomes, analyzing microbial communities, or profiling complex cellular ecosystems, GeneInsight equips you with the tools and expertise to accelerate your mission.
From sample preparation to data delivery, we support your project with end-to-end solutions tailored to your objectives. With GeneInsight, you’re not just sequencing—you’re advancing science, innovation, and global impact.
Cost-Effectiveness
Efficient sequencing of libraries already prepared by you. Ideal for researchers who’ve completed their library prep and need high-throughput, quality-controlled sequencing services with rapid turnaround times. We support various platforms and formats, including DNA, RNA, and targeted libraries.
RNA Sequencing
Unlock transcriptomic data to study gene expression, differential expression, and alternative splicing. RNA-Seq enables comprehensive insights into coding and non-coding RNAs, revealing functional elements of the genome and offering a dynamic view of cellular states across conditions or tissues.
Whole Genome Sequencing
Gain an unbiased, base-by-base view of the entire genome. WGS detects single nucleotide variants, insertions /deletions, copy number variations (CNVs) and structural variants. It’s widely used in population genetics, rare disease research, evolutionary studies, and complex trait mapping.
Whole Exome Sequencing (WES)
Focus on the protein-coding regions that account for ~1–2% of the genome but harbor ~85% of disease-causing mutations. WES is a cost-effective strategy for identifying pathogenic variants, especially in clinical diagnostics and hereditary disease research.
Single-cell Sequencing
Dissect cellular heterogeneity by profiling gene expression in thousands of individual cells. Ideal for understanding tissue composition, immune landscapes, stem cell differentiation, or tumor microenvironments. Supports droplet-based and plate-based protocols.
Spatial Transcriptomics
Bridge the gap between gene expression and tissue architecture. Spatial transcriptomics enables the localization of transcripts within intact tissue sections, preserving spatial context. It’s transformative for cancer research, developmental biology, and neuroscience.
Immune Repertoire Sequencing
Analyze T-cell and B-cell receptor diversity at high resolution. This service enables clonality assessment, immune profiling, and tracking immune responses in infection, autoimmunity, and immuno-oncology. Supports both bulk and single-cell workflows.
Epigenomics Sequencing
Interrogate the epigenetic landscape with assays such as Whole Genome Bisulfite Sequencing (WGBS), ATAC-seq, and ChIP-seq. Epigenomics helps decipher DNA methylation, chromatin structure, and histone modifications—key regulators of gene expression and cellular identity.
Oncology Panel Sequencing
Bridge the gap between gene expression and tissue architecture. Spatial transcriptomics enables the localization of transcripts within intact tissue sections, preserving spatial context. It’s transformative for cancer research, developmental biology, and neuroscience.
Long-read Sequencing
Utilize PacBio or Oxford Nanopore technologies to achieve extended read lengths and resolve complex genomic regions, including structural variants, repeat expansions, and haplotypes. Especially powerful for de novo assemblies, metagenomics, and isoform-level transcriptomics.