ENGLISH
KOREANIt provides an analysis service that allows you to analyze the sequence of a dielectric to check the variation and detailed information of a specific sequence.
Genetic mutations such as SNP, Insertion, and Deletions and various variations such as Copy Number
Variation (CNV) can be checked.
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
Genetic mutations such as SNP, Insertion, and Deletions and various variations such as Copy Number Variation (CNV) can be checked. Genetic mutations such as SNP, Insertion, and Deletions and various variations such as Copy Number Variation (CNV) can be checked.
Specialized genome analysis we offer :
- Whole Genome Sequencing
- Whole Exome Sequencing
Whole Genome Sequencing
Whole genome sequencing (WGS) is a remarkable technique that allows us to explore the complete DNA sequence of an organism. Its usage spans different fields (like healthcare and agriculture) and applications (like identifying variants and new genome assembly). Along with going through a large amount of data in a short duration, this technique generates a base-by-base representation of the genome. At 3BIGS, we provide you with an unparalleled WGS service.
Whole Exome Sequencing
Whole exome sequencing (WES) brings to light information about exons (protein-coding regions of the genome). The exome is reported to have a high density of mutations that result in diseases. This technique is widely utilized to investigate these mutations or variants, which can serve as biomarkers. The 3BIGS WES workflow is specifically designed to process voluminous data and provide coherent results of the best quality.
