Pioneer Genomic Discovery
Unlock the Secrets of the Genome with Our Comprehensive Genomics Services for Groundbreaking Research Discoveries
Our Services
Our offerings reflect the sum of our experiences, providing meaningful answers to fundamental questions.
Whole Genome Sequencing
Our Whole Genome Sequencing (WGS) service delivers a comprehensive and unbiased method of sequencing an individual’s entire genome. It’s essential for research in genomics, population genetics, and personalized medicine. Our expert team uses cutting-edge technology to provide reliable, scalable results.
Whole Exome Sequencing
Our Whole Exome Sequencing (WES) service provides a cost-effective method of sequencing the protein-coding regions of the genome. It’s essential for cancer genomics, rare disease research, and population genetics, providing a comprehensive view of genetic variation for research studies with high sensitivity to detect SNVs and indels.
Human Genotyping Arrays
Our Human Genotyping Arrays service offers a cost-effective and high-throughput method for genotyping a large number of genetic variants. It’s an essential tool for research studies in fields such as population genetics, disease association studies, and pharmacogenomics. .
Whole Transcriptome Sequencing
Our Whole Transcriptome Sequencing (WTS) service provides a method of sequencing the entire set of RNA transcripts in a sample, offering a comprehensive view of gene expression, identification of mutations, and fusion transcripts. It’s essential for transcriptomics, gene regulation, and biomarker discovery research.
mRNA Sequencing
Our mRNA Sequencing service provides insights into gene expression. It’s essential for research studies in fields such as transcriptomics, disease biology, and drug discovery, enabling a better understanding of gene regulation and its impact on human health.
microRNA Sequencing
Our miRNA Sequencing service provides a comprehensive and unbiased method for studying microRNA expression profiles. It’s essential for research studies in fields such as cancer biology, stem cell research, and neurodegenerative diseases, enabling a better understanding of the role of miRNAs in gene regulation and disease progression.
Shotgun Metagenomic Sequencing
Our shotgun metagenomic sequencing provides information on the total genomic DNA from all organisms in a sample, avoiding the need for isolation and cultivation of microorganisms or amplification of target regions. It provides information on the taxonomic annotations of each organism, and the functional profiling, gene prediction and microbial interaction of the whole community.
16S/18S/ITS Metagenomic Sequencing
Our 16S/18S/ITS Amplicon Metagenomic Sequencing service identifies microbial communities by sequencing specific regions of microbial DNA. It’s essential for microbiology, ecology, and environmental science research, providing comprehensive insights into microbiome composition. Our expert team delivers reliable results using cutting-edge technology.
De novo Sequencing
Our De novo Sequencing service offers a comprehensive and unbiased method for sequencing novel genomes without a reference genome. It’s an essential tool for research studies in fields such as genomics, evolution, and biodiversity. Our expert team uses cutting-edge technology and advanced bioinformatics tools to deliver reliable, accurate, and high-quality results for discovery.
Single Cell Sequencing
Our Single Cell Sequencing service offers a powerful and unbiased method for studying genomic and transcriptomic heterogeneity at the single-cell level. It’s essential for research studies in fields such as cancer biology, immunology, and developmental biology, enabling a better understanding of cellular diversity and its impact on human health.
Whole Genome Bisulfite Sequencing
Our Whole Genome Bisulfite Sequencing service provides a comprehensive and unbiased method for studying DNA methylation patterns across the entire genome. It’s essential for research studies in fields such as epigenetics, cancer biology, and developmental biology, enabling a better understanding of the role of DNA methylation in gene regulation and disease progression.
DNA Methylation Microarray
Our DNA Methylation Microarray service provides a high-throughput method for studying DNA methylation patterns across the entire genome. It’s essential for research studies in fields such as epigenetics, cancer biology, and developmental biology, enabling a better understanding of the role of DNA methylation in gene regulation and disease progression.
COVID-19 Variant Sequencing
Our COVID-19 Variant Sequencing service offers a targeted and high-throughput method for identifying SARS-CoV-2 mutations within the genome of sub-strains which may result in differences in infectability, severity, and vaccine response, therefore characterizing and tracking them is essential for successful surveillance and prevention.
Nucleic Acid Extractions
Our Nucleic Acid Extractions can be combined with sequencing, GWAS arrays, panels, or custom content products to provide you with an end-to-end solution for your study regardless of sample source. We offer extraction and qualification services for a wide range of sources and formats, including FFPE tissue.
Bioinformatics Analysis
Our Bioinformatics Analysis service provides a comprehensive and efficient method for analyzing large-scale genomic data generated from various sequencing platforms. It’s essential for research studies in fields such as genomics, transcriptomics, and epigenomics. Our expert team uses cutting-edge algorithms and software tools to deliver reliable, accurate, and scalable results for research studies.