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Research Services

Pioneer Genomic Discovery

Our pioneering scientists harness the power of genetic insights to accelerate targeted drug development and advance population health. Through our research services, we collaborate with leading pharmaceutical and biotech organizations to enhance R&D outcomes by integrating human genetics across every stage of discovery and development.

Collaborate with us

We act as scientific partners to help integrate human genetics into drug discovery and development. Whether identifying new targets, evaluating clinical-stage assets, or refining development strategies, AGTC Genomics delivers customised, data-driven approaches tailored to your strategic goals. Together we can accelerate drug discovery and advance population health to help people live longer, healthier lives.

Powering Discovery and development

Our offerings reflect the sum of our experiences, providing meaningful answers to fundamental questions.

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Whole Genome Sequencing (WGS)

Enables researchers to describe the full genetic composition of individuals and characterize entire human genomes.

  • Population genomics
  • Identification of somatic mutations in cancer
  • Rare disease studies
  • Biobanking projects
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Whole Exome Sequencing (WES)

Supports studies on genetic disorders, complex diseases, cancer, and human population genetics.

  • Population genomics
  • Identification of somatic mutations in cancer
  • Rare disease studies
  • Biobanking projects
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Human Genotyping Arrays

For researchers conducting large-scale genetic studies, such as genome-wide association studies (GWAS), validation of variants, and population genetics research.

  • Genome-wide association studies (GWAS)
  • Consumer genomic testing
  • Polygenic risk scores
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COVID-19 Sequencing

For diagnosis of patients suspected of novel coronavirus

  • Detection of SARS-CoV-2 virus RNA and virus genome analysis
  • ​2019-nCoV primers designed to detect RNA from the SARS-CoV-2 virus 
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De novo Sequencing

For researchers and organizations in genomics, microbiology, agriculture, medicine, ecology, and evolutionary biology.

  • Virulence research
  • Drug resistance mechanism
  • Vaccine development
  • Epidemiology
  • Microbial evolution
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Whole Transcriptome Sequencing

Offers a range of solutions tailored to your study’s needs

  • Determining differential gene expression, single nucleotide variations, and fusion gene in single run.
  • Exploring miRNA sponge and target regulatory elements.
  • Investigating regulatory networks among lncRNA/circRNA-miRNA-gene pairs.
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mRNA Sequencing

For researchers of agriculture, environment, healthcare labs etc. who use transcriptomics to solve practical challenges. 

  • Population genomics
  • Identification of somatic mutations in cancer
  • Rare disease studies
  • Biobanking projects
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microRNA Sequencing

Allows researchers to measure the abundance of miRNAs in a sample and to compare the miRNA expression levels between different samples.

  • Identification of miRNA biomarkers 
  • Characterization of miRNA-based therapeutic targets.
  • Investigating the mechanisms drug respins.
  • Study of miRNA-mediated gene regulation
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Single Cell Sequencing

For researchers and innovators who need to resolve cellular complexity beyond what bulk sequencing can reveal, especially in heterogeneous samples or rare cell populations.

  • Single Cell Gene Expression
  • Single Cell Immune Profiling 
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16S/18S/ITS Metagenomic Sequencing

For researchers who need accurate profiling of microbial communities to uncover species composition, diversity, and function.

  • Targeting and identifying the organisms of interest
  • Annotating diverse microorganisms 
  • Detection of pathogens, microorganism contamination.
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Shotgun Metagenomic Sequencing

For researchers who need unbiased, whole-community genomic insights to study microbial diversity, functions, and interactions.

  • Targeting and identifying the organisms of interest
  • Annotating diverse microorganisms 
  • Detection of pathogens, microorganism contamination
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Whole Genome Bisulfite Sequencing

For researchers in oncology, neuroscience, developmental biology, plant/animal genetics, and translational epigenetics.

  • Profiling methylation patterns 
  • Identifying differentially methylated sites 
  • Understanding mechanisms of cell differentiation
  • Detection of DNA hypermethylation 
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DNA Methylation Microarray

Assists researchers in the epigenome wide association studies.

  • Understanding the functional mechanisms at work in complex disease.
  • Detecting altered methylation patterns and epigenetic changes
  • Investigating the host methylation to infectious diseases.
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Bioinformatics Analysis

For variant detection, sequence data is aligned to available reference sequences

  • Variant Analysis
  • Transcriptome Analysis
  • Microbiome Profiling
  • Pathway & Network Analysis
  • ​Customized Analysis
     
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