Genomic Data Services
Unlocking Insights for Health and Innovation
In the intricate world of genomics, data holds the key to unravelling mysteries related to human health, diseases, and therapeutic interventions. Our genomic data science services bridge the gap between raw genetic information and actionable insights, empowering researchers, pharmaceutical pioneers, and healthcare institutions.
Why Our Genomic Data Analysis Matters
Health Understanding
Genomic data analysis provides a deeper understanding of individual health profiles. By decoding DNA sequences, we uncover genetic variations, susceptibility to diseases, and potential drug responses.
Disease Insights
From rare genetic disorders to complex diseases, our computational and statistical methods reveal patterns, biomarkers, and pathways. These insights drive precision medicine and targeted therapies.
Drug Development
Pharmaceutical companies leverage genomic data to identify drug targets, optimize clinical trials, and personalize treatments. It’s a game-changer in the quest for novel therapeutics.
How We Power Your Genomics Research
Data Analytics Solutions
We transform raw genomic data into actionable knowledge. Our team analyses large-scale datasets, identifies variants, and interprets their functional impact.
Pharma and Biotech Collaboration
Collaborate with us to accelerate drug discovery. Our expertise supports preclinical research, biomarker identification, and pharmacogenomics.
Research Institution Support
Academic and research institutions benefit from our tailored solutions. We assist in GWAS (genome-wide association studies), transcriptomics, and epigenetics research
Adding Value to Your Research:
Target Discovery
Biomarker Discovery
Pharmacogenomics
Molecular Diagnostics
Patient Stratification
Drug Repurposing
Disease Risk Prediction
Genetic Risk Prediction
Genomic Data Services
High dimensional data analysis
Genetic Variation Analysis
- WGS/WES analysis to decipher somatic and germline mutations
- Rare-Variant Association Analysis
- GWAS and haplotype analysis to facilitate the discovery of SNPs implicated in disease
- Polygenic Risk Score analysis
Gene Expression Analysis
- mRNA, miRNA exploratory analysis and visualization
Epigenetics Data Analysis
- Gaining insight into protein–DNA interactions
- Investigating methylation patterns
Pathway enrichment analysis
Multiomics Services
Integrate multiomics methods across
- Genomics
- Transcriptomics
- Epigenomics
- Single-cell genomics
Gain Deeper Insights on
- Therapeutic targets
- Novel disease-biomarkers
- Disease heterogeneity in a population
- Genotype–Phenotype associations
- Clinically actionable genetic variants
Cloud-based genomics computing
- Assist in the analysis & secure management of genomic datasets
- Design customised genomics workflows
- Access data via a web interface, APIs, or Jupyter Notebook
- Make data visualization possible in novel & creative ways
- Allow multiuser access & collaboration from anywhere
Data management services
- Data Cleaning & Knowledge Mining
- Creating FAIR data
- Mapping files & Data cataloguing
- Intake & Integration of Varied Datasets
- Building Workflows to Support Automation
- Accessing Data in different programmatic ways
- Creating collaborative & unified data science environment
Why Work with Latlon ?
Global Reach
Our services extend across borders, serving Pharma, Biotech, and Research Institutions worldwide.
Scientific Rigor
Our team comprises bioinformaticians, geneticists, and data scientists who adhere to rigorous scientific standards.
Customized Genomic Data Strategies
We blend diverse data sources, analytical methods, and tools to manage the vast array of structured, semi-structured, and unstructured data.
Privacy and Compliance
We handle sensitive genomic data with utmost confidentiality and comply with all regulatory requirements.
