Analysis Packages
Choose the right analysis for your research. Each package delivers a comprehensive report with detailed findings and interpretations.
Genomic Analysis Services
WES AnalysisWhole Exome Sequencing (WES) Analysis
- Quality control and preprocessing of raw sequencing data
- Accurate read alignment to the reference genome
- Variant calling and filtering for SNPs and Indels with quality metrics
- Functional annotation using curated clinical and population databases
CES AnalysisClinical Exome Sequencing (CES) Analysis
- Processing and QC of germline data targeting clinically relevant exons
- High-confidence variant calling for inherited disorders
- Functional annotation via curated clinical databases
- ACMG-guided germline variant classification
WGS AnalysisWhole Genome Sequencing (WGS) Analysis
- Quality control and preprocessing of WGS data
- Read alignment and variant calling for SNVs, Indels, and structural variants
- Genome-wide functional annotation and impact prediction
- Detection of clinicallyrelevant variants and known disease associations
SVA AnalysisSomatic Variant Analysis
- Detecting somatic single-nucleotide variants (SNVs) and small…
- Estimating variant allele frequency (VAF) to resolve clonal architecture…
- Functionally annotating variants with COSMIC, TCGA, OncoKB, and other…
- Calculating tumor mutational burden (TMB) and assessing microsatellite…
CNV AnalysisCopy Number Variation Analysis
- High-resolution detection of copy-number alterations from WGS…
- Identification of copy-number gains and losses
- Segmentation-based gene-level and region-level CNV analysis
- Comprehensive visualization with CNV heatmaps, genome-wide CNV plots…