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Whole Genome Resequencing

Whole genome re-sequencing 은 reference genome을 가진 종을 대상으로 특정 개체간의 변이를 분석하여 개체나 집단의 염기서열의 비교를 통해 맞춤 의학 연구활용 또는 동∙식물의 분자육종 등 다양한 곳에서 활용 가능합니다.
Whole genome re-sequencing 는 기능적 요소와 관련된 유전적 변이(SNPs, insertions, deletions) 뿐만 아니라 유전체 전반적인 구조적인 변이(inversions, complex rearrangements, copy number variation) 를 확인 할 수 있습니다.

illumina

Workflow
Sample requirements
  • Low input(10ng gDNA)
  • PCR-based(100ng or 200ng gDNA)
  • PCR-free(1µg or 2µg gDNA)
Turnaround time

About 4 weeks

Bioinformatics

Illumina 10X Genomics Additional Data Report
Whole Genome Sequencing Germline/Somatic Mutation Analysis - Whole Genome Sequencing
- Phased SNVs/indels Analysis
- Structure Variant Analysis
- Rare Variants Analysis
- HLA analysis
- Somatic Copy Number Alteration Analysis
- Sequencing Summary
- Alignment Summary
- Depth Coverage Plot
- Genotype Calling and SNP detection
- Germline & Somatic Variant Summary and Annotation
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