Services

서비스

Bioinformatics

Whole Genome Resequencing

WGRS Workflow
Insertsite Workflow

생명정보학 분석

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

생명정보학 분석

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

  • 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

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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