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KOREANOur analysis service enables you to examine dielectric sequences for specific variations and detailed information. You can identify genetic mutations such as SNPs, insertions, deletions, and various other variations like Copy Number Variations (CNV). This comprehensive analysis provides valuable insights into sequence variations and genetic mutations.
Analysis Services Features
- Quickly deliver analysis results data
- Analysis of genomic data for various species
- Use the latest Genome reference for WES analysis
- Variational Analysis Using GATK Pipeline
- Variant quality filtration
Data Analysis
- Variant calling – SNP and INDEL
- Variant annotation – SNP and INDEL
- Structural Variants (SV)
- Copy number of variants (CNV)
Genome Analysis
Identify genetic mutations such as SNPs, insertions, deletions, and variations like Copy Number Variations (CNV) with our comprehensive genome analysis services. We offer specialized solutions for detailed genomic insights.
Specialized genome analysis we offer :
- Whole Genome Sequencing
- Whole Exome Sequencing
Whole Genome Sequencing
Whole Genome Sequencing (WGS) explores an organism’s complete DNA sequence, applicable in healthcare, agriculture, and more. It identifies variants and assembles new genomes, generating a base-by-base representation quickly. At 3BIGS, we offer unparalleled WGS services for comprehensive genomic analysis.
Whole Exome Sequencing
Whole Exome Sequencing (WES) focuses on exons, the protein-coding regions of the genome, which are dense with disease-causing mutations. Widely used for identifying these variants as biomarkers, the 3BIGS WES workflow processes large data volumes, delivering high-quality, coherent results.
