BioFX - Bioinformatics Services
From BioFX Bioinformatics Services
A comprehensive suite of bioinformatics services for NGS data analysis encompassing a wide range of applications including genomics, transcriptomics, single cell genomics, immune profiling, genome assembly and annotation and more. Our team of experts combined with our advanced reporting have resulted in over 200 scientific publications in high-impact journals. Let us help you get the most out of your data.
Unlock Your Analysis Potential
BioFX Analysis Platform
- Streamlined pipelines for fast & scalable analysis
- Best-in-class Bioinformatics tools
- Interactive reports
- Publication-ready analysis outputs
- Improve data interpretation with support from MedGenome’s team of experts
BioFX - Dedicated Bioinformatics Resources
- Scalable & cost-effective resource staffing approach
- Deep biology expertise to handle your analysis requirements
- Analyze public or curated data sets
- Publication-ready analysis outputs
Explore Our Analysis Reports
A proprietary analysis platform for genomics that allows the delivery of high-quality, interpretable and interactive publication-ready figures and analysis reports. Customizable reports are available to meet every project’s requirements.
Single Cell Analysis
- Built using state-of-the-art analysis tools for gene expression, T-cell and B-cell sequencing data
- Multi-omic analysis integrates gene expression and VDJ sequencing data
- Advanced QC metrics
Transcriptome & Tumor Microenvironment Analysis
- Detailed RNA specific QC reports
- Differential expression analysis
- Pathway enrichment analysis
- Fusion and splicing event analysis with interactive genome browser to visualize results
- Proprietary tumor microenvironment analysis
Immune Repertoire Analysis
- Automated analysis workflows for bulk T-cell and B-cell sequencing
- Analyze TCR/BCR repertoires in custom species including human, horse, rat, mouse and rhesus monkey
- Detailed QC reports
- Advanced analysis outputs including V-J gene usage, clonotype diversity, clustering, CDR3 motif analysis
DNA and Whole Exome Analysis
- Germline, low-frequency somatic variant analysis and annotation
- Structural variant, copy number variant analysis and annotation
- Integrated genome browser to visualize results
- Proprietary analysis workflow to prioritize clinically-relevant variants
- Detailed QC and analysis reports
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