CNV calling from NGS data (It's one of Bioinformatics problems)
Table of Contents
관련자료 #
알려진 프로그램들 #
- Population-level variants
- Somatic CNA
관련 논문 #
- Integrative DNA copy number detection and genotyping from sequencing and array-based platforms bioRxiv 2017-08-04: NGS 방법과 SNP array 방법을 통합하여 CNV 분석
- Gene-based comparative analysis of tools for estimating copy number alterations using whole-exome sequencing data Oncotarget 2017-04-18: 유전자 중심으로 SNP array 데이터와 WES 데이터 비교
NGS based CNV 도구들 리뷰 #
- Evaluation of somatic copy number estimation tools for whole-exome sequencing data Briefings in Bioinformatics 2015-07-25
- Whole-genome CNV analysis: advances in computational approaches Frontiers in Genetics 2015-04-13
- CODEX: a normalization and copy number variation detection method for whole exome sequencing Nucleic Acids Research 2015-01-23
- An evaluation of copy number variation detection tools from whole-exome sequencing data Human Mutation 2014-02-21
- Comparative study of exome copy number variation estimation tools using array comparative genomic hybridization as control BioMed Research International 2013-11-03
- Computational tools for copy number variation (CNV) detection using next-generation sequencing data: features and perspectives BMC Bioinformatics 2013-09-13
- Computational methods for detecting copy number variations in cancer genome using next generation sequencing Oncotarget 2013-11-04
세미나 동영상 #
Estimating copy number from sequencing platforms -- overview of methods (CoNIFER, xHMM, ngCGH)
How to Detect Copy Number Variations in NGS Data and Integrate with Gene Expression Data
Incoming Links #
[Medical Scholarly Articles] About (MedicalScholarlyArticle 0) #
- Allele-specific copy number profiling by next-generation DNA sequencing
- An evaluation of copy number variation detection tools from whole-exome sequencing data
- Evaluation of somatic copy number estimation tools for whole-exome sequencing data
- Gene-based comparative analysis of tools for estimating copy number alterations using whole-exome sequencing 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
[Codes] About (Code 1) #
Related Articles (Article 2) #
Related Education Events (EducationEvent 3) #
Related Medical Scholarly Articles (MedicalScholarlyArticle 4) #
- An evaluation of copy number variation detection tools from whole-exome sequencing 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
Related Codes (Code 5) #
Suggested Pages #
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