About AccuraScience
Established in June 2013, AccuraScience was the first bioinformatics service company in the U.S. offering broad-spectrum customized bioinformatics solutions to academic and industry researchers.
We’ve since helped over 180 research organizations across five continents complete 400+ projects successfully, contributing to peer-reviewed publications, NIH-funded grants, and clinical pipelines.
Our clients include universities, hospitals, biotech companies, CROs, and pharmaceutical firms — from early-stage explorations to mission-critical programs.
Our team brings over 200 years of combined experience, and many of our Lead Bioinformaticians hold advanced degrees in both biology and computational fields, allowing us to “speak both scientific and statistical languages” fluently.
Who We Are
- - Many of our core team members have served as faculty at major U.S. institutions and worked in biotech or clinical settings (Meet our team →)
- - We work directly with PIs, scientists, and project leads to develop, execute, and refine analysis pipelines.
- - We operate entirely in-house — no outsourcing, no black-box automation.
- - Every project is guided by human expertise and biological insight.
Our Mission
Our mission is to help researchers transform complex data into usable, meaningful results — through:
- - Scientific collaboration
- - Rigorous methodology
- - Timely delivery
We do this by:
- - Translating biological questions into analytical frameworks
- - Designing or adapting pipelines tailored to your data and goals
- - Delivering reviewer-ready, well-documented outputs
- - Troubleshooting problems generic pipelines can’t handle
Whether you’re working on a grant, publication, validation study, or new product, we adapt to your timeline and context.
Our Expertise
We offer comprehensive bioinformatics services across omics types, data modalities, and study goals.
Here’s a high-level summary, with links to expert-authored blogs:
🔬 Short-Read Sequencing & Core Omics
- - Whole-genome/exome analysis, variant calling
- - RNA-seq: quantification, DE, isoforms, de novo transcriptomes
- - ATAC-seq, ChIP-seq, CUT&Tag, CUT&RUN, DNA methylation (WGBS, RRBS, EPIC, scBS-seq)
- → Epigenomics analysis blog | DNA methylation pitfalls blog
🧬 Single-Cell & Spatial Transcriptomics
- - scRNA-seq, scATAC-seq, Multiome
- - Visium, Xenium, CosMx
- → Single-cell multiome blog | Multi-omics integration blog | Spatial transcriptomics blog
🔗 Multi-Omics Integration
- - RNA + ATAC + methylation + proteomics + metabolomics
- - Correlation, enrichment, graph/network analysis, deep learning
- → Multi-omics integration blog
🧪 GWAS, EWAS, TWAS, PWAS & Population Studies
- - Full pipeline support, population structure correction, summary stats
- → GWAS 15-minute guide | GWAS troubleshooting blog | Beyond GWAS blog
🤖 AI & Structural Modeling
- - AlphaFold 2/4, CNNs, LLMs, biomarker discovery, drug response prediction
- → AlphaFold 2 blog | AlphaFold 4 blog | 10 AI use cases blog
🦠 Microbiome Analysis
- - 16S and shotgun metagenomics: taxonomic + functional profiling
- → Microbiome analysis blog
🧫 Proteomics
- - DIA/TMT pipelines, normalization, batch correction, differential abundance
- → Proteomics blog
🛠 Custom Pipelines & Troubleshooting
- - Long-read methylation, hybrid assemblies, dropout handling, peak issues
- → Troubleshooting ATAC/ChIP blog | DNA methylation pitfalls blog | Long-read integration blog
Global Reach and Impact
- - 180+ academic, biotech, and pharma clients
- - Research teams across North America, Europe, Asia, Africa, and Australia
- - Projects on human, microbial, plant, and model organism systems
Our work has contributed to:
- - Peer-reviewed papers in Nature, eLife, Cell Reports, Frontiers, and more
- - NIH and international grants
- - Clinical and regulatory programs at biotech and pharma firms
What to Expect
- ✅ Personalized expert support
- ✅ Clear deliverables and documentation
- ✅ Transparent pricing and scope
- ✅ Flexible collaboration with PIs, staff scientists, or commercial teams