CNVannotator: A Comprehensive Annotation Server for Copy Number Variation in the Human Genome
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Title
CNVannotator: A Comprehensive Annotation Server for Copy Number Variation in the Human Genome
Authors
Keywords
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Journal
PLoS One
Volume 8, Issue 11, Pages e80170
Publisher
Public Library of Science (PLoS)
Online
2013-11-15
DOI
10.1371/journal.pone.0080170
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- NGS catalog: A database of next generation sequencing studies in humans
- (2012) Junfeng Xia et al. HUMAN MUTATION
- CNVD: Text mining-based copy number variation in disease database
- (2012) Fujun Qiu et al. HUMAN MUTATION
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- (2012) Ilkka Lappalainen et al. NUCLEIC ACIDS RESEARCH
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- CNV-WebStore: Online CNV Analysis, Storage and Interpretation
- (2011) Geert Vandeweyer et al. BMC BIOINFORMATICS
- Population genetics of malaria resistance in humans
- (2011) P W Hedrick HEREDITY
- Genome structural variation discovery and genotyping
- (2011) Can Alkan et al. NATURE REVIEWS GENETICS
- DiseaseMeth: a human disease methylation database
- (2011) J. Lv et al. NUCLEIC ACIDS RESEARCH
- GWASdb: a database for human genetic variants identified by genome-wide association studies
- (2011) Mulin Jun Li et al. NUCLEIC ACIDS RESEARCH
- NCBI Reference Sequences (RefSeq): current status, new features and genome annotation policy
- (2011) K. D. Pruitt et al. NUCLEIC ACIDS RESEARCH
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- CNV Workshop: an integrated platform for high-throughput copy number variation discovery and clinical diagnostics
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- Germline copy number variation and cancer risk
- (2010) Roland P Kuiper et al. CURRENT OPINION IN GENETICS & DEVELOPMENT
- The landscape of somatic copy-number alteration across human cancers
- (2010) Rameen Beroukhim et al. NATURE
- Association of Higher DEFB4 Genomic Copy Number With Crohn's Disease
- (2009) Robert W Bentley et al. AMERICAN JOURNAL OF GASTROENTEROLOGY
- Challenges for CNV interpretation in clinical molecular karyotyping: Lessons learned from a 1001 sample experience
- (2009) Karen Buysse et al. European Journal of Medical Genetics
- ChimerDB 2.0—a knowledgebase for fusion genes updated
- (2009) Pora Kim et al. NUCLEIC ACIDS RESEARCH
- Potential etiologic and functional implications of genome-wide association loci for human diseases and traits
- (2009) L. A. Hindorff et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Excessive genomic DNA copy number variation in the Li-Fraumeni cancer predisposition syndrome
- (2008) A. Shlien et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
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