Where curiosity
meets clarity

Powerful spectrum of analysis services for genomics led by top global scientists as recognized by a significant number of peer reviewed publications.

Advance your genomic research

Genuity Science delivers interpretation and actionable insights for whole genome sequencing (WGS), whole exome sequencing (WES), or transcriptome sequencing data through our Genomic Analysis Services. Advance your genomic research with our streamlined secondary and tertiary analysis services.

Available Services

Whole Genome Sequencing (WGS) and Whole Exome Sequencing (WES) Data Analysis

Secondary Analysis​

  • Reference genome alignment to hg38 or hg19​
  • SNV/Indel variant calls using Sentieon​
  • Copy number variation (CNV) calls using CNVkit​
  • Somatic: tumor only or tumor/normal comparison

Tertiary Analysis​

  • QC analysis: sample and variant overall quality/coverage, HWE, relatedness, sex check​
  • Variant annotations from over 30 reference sources​

Germline Variant Analysis​

  • Target gene validation: variant/gene prioritization, disease associations​​
  • Cohort analysis: variant/gene-based association studies, PheWAS

Somatic Variant Analysis

  • Driver gene identification​
  • Tumor mutation burden (TMB)​
  • Microsatellite instability (MSI)​

Transcriptome Sequencing Data Analysis for Bulk and Single Cell RNA

Secondary Analysis​

  • Reference genome alignment to hg38 or hg19​
  • Transcript quantification using RSEM
  • Alternate splicing analysis (requires minimal 50M PE reads) – human only

Tertiary Analysis​

  • Differential gene expression analysis with EdgeR​​
  • Functional enrichment: GOseq/nGOseq for pathway analysis​
  • Network analysis

Artificial Intelligence​

Learn more about our AI solutions for advanced single cell RNASeq and multi-omic analyses.