Gene-based comparative analysis of tools for estimating copy number alterations using whole-exome sequencing data
#
Find similar titles
- (rev. 2)
- Hyungyong Kim
Structured data
- About
- CNV calling from NGS data
- Date Published
- Publisher
- Oncotarget
- URL
- https://www.ncbi.nlm.nih.gov/pubmed/28460482
Exome sequencing 데이터에서 CNA 추정하는 프로그램들 평가 - TCGA 데이터로 SNP6 데이터를 정답으로 보고, 일치율을 비교함
saasCNV가 가장 좋은 성능을 보임.
관련 포스트
Incoming Links #
Related Articles (Article 0) #
Suggested Pages #
- 0.121 Allele-specific copy number profiling by next-generation DNA sequencing
- 0.103 Evaluation of somatic copy number estimation tools for whole-exome sequencing data
- 0.025 Python 3
- 0.025 July 25
- 0.025 PennCNV
- 0.025 April 22
- 0.025 Ageing
- 0.025 CODEX: a normalization and copy number variation detection method for whole exome sequencing
- 0.025 matplotlib
- 0.025 R
- More suggestions...