PearlOmics is a Bioinformatics Research & Innovation Centre focused on bioinformatics, computational biology, teaching, research, and scientific communication. We bridge the gap between higher education, research, and industry through practical training, research support, and scientific expertise.
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End-to-end multi-omics pipelines—from high-throughput library prep and deep sequencing to publication-ready bioinformatic workflows tailored for academia, biotech, and clinical research.
Explore our full range of genomics services — scope, deliverables, and analytical pipelines curated by domain experts.
Comprehensive de novo assembly, structural variant discovery, and full-genome mutation mapping for microbes, plants, and mammalian systems.
Targeted deep sequencing of protein-coding regions for clinical diagnostics, rare disease genetics, and somatic oncology mutations.
Cost-effective high-density marker discovery for population genetics, QTL mapping, and molecular breeding programs.
Total RNA / mRNA sequencing to quantify gene expression dynamics, novel isoform detection, and alternative splicing events across any biological system.
High-resolution cellular heterogeneity profiling to resolve rare sub-populations and trajectory lineages at single-cell resolution.
Genome-wide mapping of open chromatin regions to pinpoint active promoters, enhancers, and transcription factor footprints.
Single-base resolution of DNA methylation (5mC/5hmC) to uncover epigenetic regulation in development and disease.
Taxonomic composition and functional gene potential across gut, environmental, soil, or clinical microbiome samples using amplicon and whole-metagenome approaches.
A rigorous, transparent four-phase pipeline that guarantees reproducibility, data integrity, and interpretive clarity.
