标题
Family-Based Benchmarking of Copy Number Variation Detection Software
作者
关键词
-
出版物
PLoS One
Volume 10, Issue 7, Pages e0133465
出版商
Public Library of Science (PLoS)
发表日期
2015-07-22
DOI
10.1371/journal.pone.0133465
参考文献
相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。- Deep Whole-Genome Sequencing of 100 Southeast Asian Malays
- (2013) Lai-Ping Wong et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Computational tools for copy number variation (CNV) detection using next-generation sequencing data: features and perspectives
- (2013) Min Zhao et al. BMC BIOINFORMATICS
- Five Years of GWAS Discovery
- (2012) Peter M. Visscher et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Software comparison for evaluating genomic copy number variation for Affymetrix 6.0 SNP array platform
- (2011) Jeanette E Eckel-Passow et al. BMC BIOINFORMATICS
- Mapping copy number variation by population-scale genome sequencing
- (2011) Ryan E. Mills et al. NATURE
- Comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variants
- (2011) Dalila Pinto et al. NATURE BIOTECHNOLOGY
- Accuracy of CNV Detection from GWAS Data
- (2011) Dandan Zhang et al. PLoS One
- Copy Number Variation across European Populations
- (2011) Wanting Chen et al. PLoS One
- VEGA: variational segmentation for copy number detection
- (2010) Sandro Morganella et al. BIOINFORMATICS
- A multilevel model to address batch effects in copy number estimation using SNP arrays
- (2010) R. B. Scharpf et al. BIOSTATISTICS
- R-Gada: a fast and flexible pipeline for copy number analysis in association studies
- (2010) Roger Pique-Regi et al. BMC BIOINFORMATICS
- Reference-unbiased copy number variant analysis using CGH microarrays
- (2010) Young Seok Ju et al. NUCLEIC ACIDS RESEARCH
- Towards a comprehensive structural variation map of an individual human genome
- (2010) Andy W Pang et al. GENOME BIOLOGY
- A single-array preprocessing method for estimating full-resolution raw copy numbers from all Affymetrix genotyping arrays including GenomeWideSNP 5 & 6
- (2009) Henrik Bengtsson et al. BIOINFORMATICS
- The first Korean genome sequence and analysis: Full genome sequencing for a socio-ethnic group
- (2009) S.-M. Ahn et al. GENOME RESEARCH
- Sequence and structural variation in a human genome uncovered by short-read, massively parallel ligation sequencing using two-base encoding
- (2009) K. J. McKernan et al. GENOME RESEARCH
- Population-genetic nature of copy number variations in the human genome
- (2009) Mamoru Kato et al. HUMAN MOLECULAR GENETICS
- Finding the missing heritability of complex diseases
- (2009) Teri A. Manolio et al. NATURE
- Deletion of the late cornified envelope LCE3B and LCE3C genes as a susceptibility factor for psoriasis
- (2009) Rafael de Cid et al. NATURE GENETICS
- Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants
- (2009) Sekar Kathiresan et al. NATURE GENETICS
- Single nucleotide polymorphism arrays: a decade of biological, computational and technological advances
- (2009) T. LaFramboise NUCLEIC ACIDS RESEARCH
- Whole Genome Distribution and Ethnic Differentiation of Copy Number Variation in Caucasian and Asian Populations
- (2009) Jian Li et al. PLoS One
- Estimation and assessment of raw copy numbers at the single locus level
- (2008) H. Bengtsson et al. BIOINFORMATICS
- Personal genomes: The case of the missing heritability
- (2008) Brendan Maher NATURE
- The diploid genome sequence of an Asian individual
- (2008) Jun Wang et al. NATURE
- Large recurrent microdeletions associated with schizophrenia
- (2008) Hreinn Stefansson et al. NATURE
- Mapping and sequencing of structural variation from eight human genomes
- (2008) Jeffrey M. Kidd et al. NATURE
- Accurate whole human genome sequencing using reversible terminator chemistry
- (2008) David R. Bentley et al. NATURE
- Deletion polymorphism upstream of IRGM associated with altered IRGM expression and Crohn's disease
- (2008) Steven A McCarroll et al. NATURE GENETICS
- Integrated detection and population-genetic analysis of SNPs and copy number variation
- (2008) Steven A McCarroll et al. NATURE GENETICS
- Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs
- (2008) Joshua M Korn et al. NATURE GENETICS
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