The high demand for low-cost sequencing has driven the development of High-throughput sequencing (or Next-generation sequencing) technologies that parallelize the sequencing process, producing thousands or millions of sequences concurrently. (Next-generation sequencing)
대용량 DNA sequencing 기술
보통 FASTQ -> BAM -> VCF or GFF3의 단계로 분석됨.
VCF 이후의 분석
NGS applications
Table of Contents
관련 링크 #
자료 #
- 「NGS 검사의 임상적 변이해석 및 검증방법 해설서」(민원인 안내서)
- 차세대염기서열분석(NGS) 임상검사실 인증 가이드라인
- 차세대 시퀀싱 기술의 10년
- PMI 현실화를 위한 NGS informatics 로드맵 신수용
- The Real Cost of Sequencing
- Web Collection: Archive : Nature Review Genetics - Clinical application for NGS: NGS의 임상응용 리뷰 모음
- de novo Assembly from NGS data
- WG3: Softwares: 분석 프로그램 모음
- Coverage and Read Depth Recommendations by Sequencing Application: NGS 어플리케이션별 추천 Depth
논문 #
- NGSCheckMate: software for validating sample identity in next-generation sequencing studies within and across data types Nucleic Acids Research : 샘플이 바뀌는지 체크
- Coming of age: ten years of next-generation sequencing technologies Nature Reviews Genetics : NGS 기술 요약 리뷰
보고서 #
Incoming Links #
Related Social Events (SocialEvent 0) #
[Medical Scholarly Articles] About (MedicalScholarlyArticle 1) #
Related Corporations (Corporation 2) #
[Codes] About (Code 3) #
Related Blogs (Blog 4) #
Related Datasets (Dataset 5) #
[Blogs] About (Blog 6) #
Related Software Applications (SoftwareApplication 7) #
Related Articles (Article 8) #
- CNV calling from NGS data
- Cancer genomics
- Cell-free tumor DNA
- ChIP-seq
- FASTQ
- Genetic testing
- Genotyping by sequencing
- Haplotype
- Human leukocyte antigen
- Loss-of-function variant
- Non-invasive prenatal test
- Opportunities and challenges of whole-genome and -exome sequencing
- Pathology
- Personalized medicine
- Rep-seq
- Reprogramming
- SNV calling from NGS data
- SRA
- Single cell sequencing
- WGS
- 암 맞춤의학과 생물정보학
Related Education Events (EducationEvent 9) #
Related Web Pages (WebPage 10) #
Related Government Organizations (GovernmentOrganization 11) #
Related Medical Scholarly Articles (MedicalScholarlyArticle 12) #
- Allele-specific copy number profiling by next-generation DNA sequencing
- Analytical and Clinical Validation of a Digital Sequencing Panel for Quantitative, Highly Accurate Evaluation of Cell-Free Circulating Tumor DNA
- CODEX: a normalization and copy number variation detection method for whole exome sequencing
- Comparison of custom capture for targeted next-generation DNA sequencing
- Computational methods for detecting copy number variations in cancer genome using next generation sequencing
- Detecting very low allele fraction variants using targeted DNA sequencing and a novel molecular barcode-aware variant caller
- Genetic alterations of triple negative breast cancer by targeted next-generation sequencing and correlation with tumor morphology
- Identification of cancer-driver genes in focal genomic alterations from whole genome sequencing data
- Next-Generation Sequencing of Circulating Tumor DNA for Early Cancer Detection
- Practical guidelines for the comprehensive analysis of ChIP-seq data
- SAAS-CNV: A Joint Segmentation Approach on Aggregated and Allele Specific Signals for the Identification of Somatic Copy Number Alterations with Next-Generation Sequencing Data
- The cancer genome
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