We provide advanced NGS data interpretation, workflow management, clinical reporting and automated interpretation tools
The only one stop cloud solution for transferring, managing and interpreting Next Generation Sequencing
Enriching detection of variants for rare diseases by associated genes
Out of the box multiple analysis, designed specifically to assess both SNP mutations and structural variants
Fully customizable or ready-to-use integrated templates for routine testing, family analysis, prenatal, tumor and case control
Association (GWAS), imputing, linkage, population stratification and functional annotation of variants/mutations
Enhancing variant search by aggregating data from multiple public and internal databases
Analyzing microarray, RNAseq, or real-time PCR data, explore gene-to- disease associations, and enrich for pathways, biological processes, and diseases
Reducing raw genomic data up to 85% of its original size and achieving 10x faster genomic data transfer utilizing existing infrastructure
“I hold the safety of my patients highest. Working with Genoox gives me confidence as their uncompromising validations experiments are vast. I can easily understand the meaning of each of the reported variants and parameters due to their friendly and comprehensive user interface.”
“Genoox delivered us with faster and more accurate genomic testing results. Collaborating with Genoox increased our capacity to manage and interpret the number of genomic results”
“The Genoox platform provides us an efficient data analysis workflow, allowing for fast and accurate results and management of our internal database.”
“Genoox is a comprehensive, user-friendly, end-to-end NGS analysis platform for human genomic studies, the Genoox platform made a massive impression, It was efficient and provided fast and accurate results“
“The Genoox platform provides us with high quality interpretation of genetic data and precise diagnosis by leveraging knowledge from first-class data sources.”
