Services

Bioinformatics

Whole Genome Resequencing Whole Exome Sequencing Targeted Sequencing

Whole Genome Resequencing

WGRS Workflow
Insertsite Workflow

Bioinformatics

Standard Analysis

Read mapping

Variants calling

Variant annotation

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Standard Analysis

Advanced Analysis

Somatic variants calling

Copy number variants (CNV)

Structure variants (SV)

Multisample variants calling

Integration site analysis

Advanced Analysis

Whole Exome Sequencing

Workflow

Bioinformatics

Standard Analysis

Raw read processing

Read mapping + BQSR, VQSR

Variant calling (SNV, Indels)

Variant annotation

Somatic mutation calling (For cancer genome only)

Standard Analysis

Advanced Analysis

Oncoplot

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Advanced Analysis

Targeted Sequencing

Workflow
Targeted Sequencing

Features & Benefits

  • Variant detection for Targeted Sequencing Panels for clinical testing purposes
  • Variant detection confirmed through national cancer information projects
  • Providing guidance in the decision-making process for disease treatment of patients by clinicians through variant discovery.

Bioinformatics

Standard Analysis

Read mapping

Variant calling

Variant annotation

Clinical report


Advanced Analysis

Genomic rearrangement

Tumor mutation Burden (TMB), Microsatellite instability (MSI)

Standard Analysis
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