Understanding Today. Transforming Tomorrow.
Official Portal: hgomics.com
Empowering Precision Medicine through Genomic Intelligence & Bioinformatics
HG-Omics bridges high-throughput whole-genome sequencing analysis with accessible, hands-on university fellowship programs. Explore our interactive gene screeners, pipeline workflow simulators, and nationwide university ambassador network.
Center for Human Genomics & Omics Research
“Uncover. Understand. Empower.”
HG-Omics provides end-to-end integrated solutions — from sample extraction to high-throughput sequencing & clinical molecular diagnostics under one roof.
Comprehensive Sample & Specimen Support
Advanced sequencing and multi-omics services tailored for diverse biological specimen domains:
GENOMIC SEQUENCING & OMICS SERVICES12 Core Offerings
Publication-grade DNA/RNA extraction, Sanger sequencing, metagenomics, transcriptomics, and custom synthesis.
PCR Product Sequencing
Sanger sequencing for PCR products with high accuracy and quality.
DNA Barcoding
Species identification using standard barcoding markers (COI, rbcL, matK, ITS).
Metagenomics
16S, 12S, 18S, COI & Shotgun Metagenomics
Metagenomics for microbial community profiling and functional analysis.
Whole Genome Sequencing (WGS) & Re-sequencing
De novo sequencing, re-sequencing and comparative genomics with comprehensive analysis.
Transcriptomics
RNA-Seq, Whole RNA-Seq, scRNA-Seq
Gene expression profiling, differential expression and pathway analysis.
Whole Exome Sequencing (WES), WGBS, SNP Array
Exome sequencing, methylation profiling (WGBS) and SNP genotyping services.
Clinical Genomics
Genetic testing and interpretation for disease diagnosis, risk assessment and precision medicine.
Proteogenomics
Integrated analysis of proteomics and genomics for functional insights and biomarker discovery.
Mitochondrial / Chloroplast Sequencing
Complete mitochondrial and chloroplast genome sequencing and analysis.
Variant Analysis & Epigenetics Sequencing
SNP, InDel, CNV calling, variant annotation and epigenetic profiling (methylation, ChIP-Seq etc.).
Primer Synthesis / Gene Synthesis / gRNA Synthesis
Custom primer design and synthesis, gene synthesis and gRNA synthesis services.
Molecular Biology Lab Chemicals & Consumables
High-quality reagents, kits and consumables for molecular biology and genomics research.
34 Specialized Molecular Diagnostic Tests
RT-PCR, Mutation Profiling, Hereditary Panels, and Clinical Metagenomics for healthcare providers & clinical research.
Dengue Virus RT-PCR Test
Category: Infectious DiseasesSARS-CoV-2 RT-PCR Test
Category: Infectious DiseasesInfluenza A/B RT-PCR Test
Category: Infectious DiseasesRespiratory Syncytial Virus (RSV) PCR Test
Category: Infectious DiseasesHepatitis B Virus (HBV) DNA PCR Test
Category: Infectious DiseasesHepatitis C Virus (HCV) RNA PCR Test
Category: Infectious DiseasesHIV-1 Viral Load Test
Category: Infectious DiseasesHPV DNA Test
Category: Infectious DiseasesTuberculosis (TB) Molecular Test
Category: Infectious DiseasesChlamydia trachomatis PCR Test
Category: Infectious DiseasesNeisseria gonorrhoeae PCR Test
Category: Infectious DiseasesMalaria PCR Test
Category: Infectious DiseasesEpstein–Barr Virus (EBV) PCR Test
Category: Infectious DiseasesCytomegalovirus (CMV) PCR Test
Category: Infectious DiseasesHerpes Simplex Virus (HSV) PCR Test
Category: Infectious DiseasesClostridioides difficile PCR Test
Category: Infectious DiseasesMethicillin-Resistant Staphylococcus aureus (MRSA) PCR Test
Category: Infectious DiseasesBRCA1/BRCA2 Mutation Test
Category: Genetic & Inherited DisordersFactor V Leiden Mutation Test
Category: Genetic & Inherited DisordersThalassemia Mutation Test
Category: Genetic & Inherited DisordersSickle Cell Disease Molecular Test
Category: Genetic & Inherited DisordersCystic Fibrosis Genetic Test
Category: Genetic & Inherited DisordersHuntington Disease Genetic Test
Category: Genetic & Inherited DisordersDuchenne Muscular Dystrophy Genetic Test
Category: Genetic & Inherited DisordersFragile X Syndrome Genetic Test
Category: Genetic & Inherited DisordersHereditary Cancer Gene Panel Test
Category: Oncology & Precision ProfilingPharmacogenomic Testing
Category: Oncology & Precision ProfilingLeukemia Mutation Panel
Category: Oncology & Precision ProfilingLung Cancer Molecular Profiling Test
Category: Oncology & Precision ProfilingColorectal Cancer Molecular Profiling Test
Category: Oncology & Precision ProfilingWhole-Exome Sequencing (WES) Diagnostic Test
Category: Clinical NGS DiagnosticsWhole-Genome Sequencing (WGS) Diagnostic Test
Category: Clinical NGS DiagnosticsClinical Microbial Whole-Genome Sequencing Test
Category: Clinical NGS DiagnosticsMetagenomic Pathogen Detection Test
Category: Clinical NGS DiagnosticsStreamlined 6-Step Multi-Omics Process
We guide your research and diagnostic projects seamlessly from physical sample collection through rigorous bioinformatics reporting.
Sample Collection
Collection & safe preservation of tissue, blood, soil, water, or microbial samples.
DNA/RNA Extraction
High-yield, ultra-pure genomic DNA or RNA isolation in our dedicated lab facility.
High-Throughput Sequencing
Next-Generation & Long-Read sequencing on cutting-edge platforms.
Bioinformatics Analysis
Quality trimming, alignment, variant calling, assembly & functional annotation.
Publication-Standard Report
Clear data visualizations, statistical rigor & ready-for-submission reports.
Data Interpretation & Research Support
Expert consultation to help interpret biological insights for publications.
We ensure high-quality data, accurate analysis, and reliable results that meet international standards for research, publication, and clinical reporting.
WHY CHOOSE HG-OMICS?
Combining world-class lab infrastructure with experienced bioinformatics scientists under one roof.
LET US EMPOWER YOUR RESEARCH AND DISCOVERIES THROUGH ADVANCED GENOMICS & DIAGNOSTICS!
HG-Omics: Empowering Genomics for a Healthier, Sustainable Tomorrow
Featured Omics Training Programs
Curated hands-on modules designed by HG-Omics researchers covering NGS pipelines, transcriptomics, and Bio-AI.
Human Whole-Genome & Exome Sequencing Analysis
Master FASTQ QC, BWA alignment, GATK best practices, VCF variant calling, and annotation using ANNOVAR and ClinVar.
Bulk & Single-Cell Cancer Transcriptomics
Explore RNA-Seq differential expression with DESeq2, pathway enrichment analysis (GSEA), and single-cell RNA analysis using Seurat.
Python & Machine Learning in Precision Medicine
Build predictive machine learning models using Scikit-Learn and PyTorch for drug target screening and phenotype classification.
Interactive Gene & Variant Bio-Screener Tool
Filter genomic variants across ClinVar, dbSNP, and expression change benchmarks in real time. Simulate next-generation sequencing workflows from FastQC to variant annotation.
Campus Representatives Showcase
Student ambassadors representing HG-Omics across premier universities & medical institutes.
2026Md Foisal Imtiaz
Campus Representative
2026Mosammat Fahmida Akter Esha
Campus Representative
2026Md Lisan Islam Bhadhon
Campus Representative
2026Zidni Al Nahian Alif
Campus Representative
Research Coordinators & Division Leads
Leading multi-omics initiatives across human genetics, cancer transcriptomics, metagenomics, and bio-AI infrastructure.
Sabekun Naher
Industrial Coordinator
Emami Bangladesh Limited (Officer, Microbiologist)
Md. Elias Hossain
Industrial Coordinator
NIPRO JMI Pharma Ltd. (Executive, Microbiology)
Akbar Hossain Chowdhury
Director of Finance
Center for Human Genomics & Omics Research (Ex. Senior Officer, Sonali Bank)
Md. Shakil Ahemed
Industrial Coordinator
Square Pharmaceuticals PLC. (Executive, Global Regulatory Affairs)
Featured Research Publications
Peer-reviewed contributions to human population genetics, precision oncology, and computational biology.
Whole-Genome Landscape and Germline Susceptibility Markers in South Asian Population Cohorts
Comprehensive high-throughput whole-genome sequencing of 1,500 individuals revealed novel population-specific single nucleotide variants (SNVs) associated with metabolic traits and hereditary cancer susceptibility.
Single-Cell RNA-Seq Uncovers Microenvironmental Heterogeneity in Triple-Negative Breast Cancer
Characterizing 45,000 single-cell transcriptomic profiles identified tumor-infiltrating lymphocyte subtypes associated with anti-PD1 therapy response rates.
Ready to Advance Your Genomics Career?
Join the HG-Omics fellowship network, apply to become a Campus Representative at your university, or explore our interactive bio-screener tools.