At the Human Genome Sequencing Center, we offer a comprehensive range of capabilities to support your genomic research and applications. Our state-of-the-art facilities and expert team provide
High-throughput Sequencing
Fast and accurate sequencing of genomes, transcriptomes and epigenomes
Bioinformatics
Customized data analysis, visualization and interpretation
Consultation and Collaboration
Expert guidance and support for study design, data analysis and result interpretation
Multiple Sequencing Platforms
Our fleet of world-class sequencers provides a scalable response to meet any need
Whether you're a researcher, a clinician, or an industry professional, we have a multitude of capabilities to support your genomic needs and advance your discoveries.
Genomics
Our genomic offerings allow researchers, clinicians and industry leaders to harness the power of genomics and drive innovation in fields like precision medicine, biotechnology, and environmental science.
Dive into the complexities of human biology with our cutting-edge genomic solutions. Explore the human genome to gain insights into inherited traits, disease susceptibility and personalized medicine.
Analyze microbial communities, identify novel species and gain insights into the intricate relationships between microbes and their environments.
A tool to compare and contrast genomes across species to understand evolutionary relationships, identify conserved regions and uncover novel biological mechanisms.
Multiomics
Our expertise in integrating multiple omics technologies to decipher the intricate relationships between genes, proteins, metabolites, and other biomolecules enables researchers to gain a comprehensive understanding and uncover hidden patterns across different omics layers.
By analyzing structure, function and interactions of proteins, researchers can understand cellular processes and disease mechanisms and identify biomarkers for diagnosis and treatment.
Analyzing metabolites provides insights into cellular metabolism and function, helps identify biomarkers for disease diagnosis and treatment, and elucidates the effects of environmental factors on metabolism.
Methylation data play a key role in understanding disease and provide insights into how gene expression changes over time or due to environmental factors.
Bioinformatics
Our expertise in integrating multiple omics technologies to decipher the intricate relationships between genes, proteins, metabolites, and other biomolecules enables researchers to gain a comprehensive understanding and uncover hidden patterns across different omics layers.
De novo assembly, reference-guided assembly and hybrid approaches tailored to fit your research goals.
Identification, annotation and prioritization of genetic variants for studies at any scale or scope.
RNA-seq, microarray and qRT-PCR data analysis provide insights into how genes are regulated and how they contribute to biological processes, development and disease.
Understanding the genetic changes that drive disease provides data to help identify cancer driver mutations, understand disease mechanisms, develop targeted therapies and monitor treatment response.
SV analysis enables the detection and interpretation of large-scale genomic rearrangements. We have developed approaches to identify SVs in short and long read data and merge SVs in large datasets.
Studying changes in gene function that occur without altering the underlying DNA sequence with ChIP-seq, ATAC-seq and DNA methylation analysis.