Multi-Omic Insights Simplified Tools

Skygenic Solutions

what sets skygenic apart

Other software platforms claim to offer user-friendly graphical interfaces, yet our scientists found they are built from a bioinformatics perspective—evident in their 1,000+ tools and focus on extensive capabilities. Skygenic bridges this gap by prioritizing simplicity and guidance, supporting the most commonly used multi-omic strategies. Designed from a biological perspective rather than a bioinformatics one, Skygenic empowers scientists to navigate analyses with ease. 

Raw data

or

Guided Analysis

or

Guided insight

Global Resources

Multipe Sources

Secure Data

Each member’s data remains secure and inaccessible to others, yet can be seamlessly combined for collaborative analysis when needed. 

Real-Time

Each member’s data remains secure and inaccessible to others, yet can be seamlessly combined for collaborative analysis when needed. 

Smart Navigation

Wizards ask biologically relevant questions to guide a scientist to the appropriate pipeline and parameters. 

Other software stops here

Automated Analysis

An automatically generated report helps scientists review results, adjust parameters, and gain insights using the same methodology as a bioinformatician’s thought process.  

Dynamic Visualization

Interactive data tables and graphs enable scientists to focus on relevant genes and results. Visualization tools are tailored to the research question, ensuring all necessary resources are utilized effectively. 

Expanded Knowledge

To deepen their understanding, scientists are connected with additional resources relevant to their research questions—resources they may not be aware of but should utilize. These include genotype-to-phenotype analysis, protein and gene functional enrichment analysis, and more.  

Multipe Sources

Secure Data

Each member’s data remains secure and inaccessible to others, yet can be seamlessly combined for collaborative analysis when needed. 

Real-Time

Each member’s data remains secure and inaccessible to others, yet can be seamlessly combined for collaborative analysis when needed. 

Smart Navigation

Wizards ask biologically relevant questions to guide a scientist to the appropriate pipeline and parameters. 

Automated Analysis

An automatically generated report helps scientists review results, adjust parameters, and gain insights using the same methodology as a bioinformatician’s thought process.  

Dynamic Visualization

Interactive data tables and graphs enable scientists to focus on relevant genes and results. Visualization tools are tailored to the research question, ensuring all necessary resources are utilized effectively. 

Expanded Knowledge

To deepen their understanding, scientists are connected with additional resources relevant to their research questions—resources they may not be aware of but should utilize. These include genotype-to-phenotype analysis, protein and gene functional enrichment analysis, and more.  

Multipe Sources

Secure Data

Each member’s data remains secure and inaccessible to others, yet can be seamlessly combined for collaborative analysis when needed. 

Real-Time

Each member’s data remains secure and inaccessible to others, yet can be seamlessly combined for collaborative analysis when needed. 

Smart Navigation

Wizards ask biologically relevant questions to guide a scientist to the appropriate pipeline and parameters. 

Automated Analysis

An automatically generated report helps scientists review results, adjust parameters, and gain insights using the same methodology as a bioinformatician’s thought process.  

Dynamic Visualization

Interactive data tables and graphs enable scientists to focus on relevant genes and results. Visualization tools are tailored to the research question, ensuring all necessary resources are utilized effectively. 

Expanded Knowledge

To deepen their understanding, scientists are connected with additional resources relevant to their research questions—resources they may not be aware of but should utilize. These include genotype-to-phenotype analysis, protein and gene functional enrichment analysis, and more.  

Multipe Sources

Secure Data

Each member’s data remains secure and inaccessible to others, yet can be seamlessly combined for collaborative analysis when needed. 

Real-Time

Each member’s data remains secure and inaccessible to others, yet can be seamlessly combined for collaborative analysis when needed. 

Smart Navigation

Wizards ask biologically relevant questions to guide a scientist to the appropriate pipeline and parameters. 

Automated Analysis

An automatically generated report helps scientists review results, adjust parameters, and gain insights using the same methodology as a bioinformatician’s thought process.  

Dynamic Visualization

Interactive data tables and graphs enable scientists to focus on relevant genes and results. Visualization tools are tailored to the research question, ensuring all necessary resources are utilized effectively. 

Expanded Knowledge

To deepen their understanding, scientists are connected with additional resources relevant to their research questions—resources they may not be aware of but should utilize. These include genotype-to-phenotype analysis, protein and gene functional enrichment analysis, and more.  

Multi-Omic Sequencing Capabilities

Comprehensive Variant Analysis

Detect and characterize germline and somatic variants in whole-genome and whole-exome sequencing data to advance disease research, personalized medicine, and clinical diagnostics.

DNA Methylation Analysis

Processes whole-genome bisulfite sequencing (WGBS) and targeted methylation sequencing data to study epigenetic modifications and their impact on gene regulation.

Viral Genome Sequencing & Surveillance

Viral genome assembly, variant calling, and phylogenetic analysis for outbreak surveillance and infectious disease research.

Genomic Insights for Rare Disorders

Perform variant calling and prioritization for rare disease research, integrating WGS/WES data with annotation tools to identify pathogenic mutations.

Targeted Amplicon Sequencing

Detect and characterize germline and somatic variants in whole-genome and whole-exome sequencing data to advance disease research, personalized medicine, and clinical diagnostics.

Microbial Taxonomy Profiling

Identify microbial composition and diversity from metagenomic sequencing data, enable microbiome research in health, agriculture, and environmental sciences.

Immune Repertoire Sequencing

Analyze adaptive immune receptor repertoire (AIRR) sequencing data to study B-cell and T-cell diversity, aiding in immunotherapy and vaccine research.

Differential Gene Expression Analysis

Perform bulk RNA sequencing analysis, including transcript quantification, differential expression, and functional enrichment of gene pathways.

Fusion Gene Detection

Detect and characterize gene fusions from RNA sequencing data, aiding in cancer research and biomarker discovery.

Chromatin Accessibility Profiling

Analyze ATAC-seq data to identify open chromatin regions, transcription factor binding sites, and regulatory elements influencing gene expression.

Single-Cell Transcriptomics & Interpretation

Process scRNA data, cell classification, gene expression profiling, differential expression analysis, integrate clustering, trajectory inference, and functional enrichment analysis.

CRISPR Screening Analysis

Analyze CRISPR knockout, knockdown, and activation screening data, identifying guide RNA efficiency and gene essentiality from sequencing data.