Exome sequencing

Exome-seq Data Analysis

Exome sequencing is a cost-effective approach when whole-genome sequencing is not practical or necessary. It is a quick and effective strategy to identify disease-causing genes for rare Mendelian disorders. It is also being applied to profile all variants in complex diseases such as Cancer and Diabetes. TACGenomics use the cutting-edge pipeline to analyze your Exome-seq data. We put more attention to quality control and data visualization.

The services for WES seq data analysis includes:
01

Germline SNV/Indel calling for individual sample

02

Somatic SNV/Indel/copynumber calling for paired samples

03

De novo germline variants calling in trio studies

04

Variant phenotype association test

05

CoMut and Circos plotting (if appliable)

06

SNV/Indel calling for Whole genome sequencing

Germline SNV/Indle Calling

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Somatic SNV/Indel Calling

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