Services
서비스
Bioinformatics
Whole Genome Resequencing
- WGRS Workflow
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- Insertsite Workflow
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생명정보학 분석
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Standard Analysis
Read mapping
Variants calling
Variant annotation
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Advanced Analysis
Somatic variants calling
Copy number variants (CNV)
Structure variants (SV)
Multisample variants calling
Integration site analysis
Whole Exome Sequencing
- Workflow
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생명정보학 분석
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Standard Analysis
Raw read processing
Read mapping + BQSR, VQSR
Variant calling (SNV, Indels)
Variant annotation
Somatic mutation calling (For cancer genome only)
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Advanced Analysis
Oncoplot
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Targeted Sequencing
- Workflow
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Features & Benefits
- 임상 검사의 목적의 Targeted Sequencing Panel에 대한 변이체 탐색
- 국가 암 정보과제로 증명된 변이체 탐색
- 변이체 발굴을 통하여 임상의들의 환자 질병 치료에 대한 의사결정 과정에 가이드 제공
생명정보학 분석
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Standard Analysis
Read mapping
Variant calling
Variant annotation
Clinical report
Advanced Analysis
Genomic rearrangement
Tumor mutation Burden (TMB), Microsatellite instability (MSI)
