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
Lai-Ping Wong et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2013)
dbVar and DGVa: public archives for genomic structural variation
Ilkka Lappalainen et al.
NUCLEIC ACIDS RESEARCH (2013)
The UCSC Genome Browser database: extensions and updates 2013
Laurence R. Meyer et al.
NUCLEIC ACIDS RESEARCH (2013)
ArrayExpress update-trends in database growth and links to data analysis tools
Gabriella Rustici et al.
NUCLEIC ACIDS RESEARCH (2013)
Database resources of the National Center for Biotechnology Information
Abigail Acland et al.
NUCLEIC ACIDS RESEARCH (2013)
Ensembl 2013
Paul Flicek et al.
NUCLEIC ACIDS RESEARCH (2013)
NCBI GEO: archive for functional genomics data sets-update
Tanya Barrett et al.
NUCLEIC ACIDS RESEARCH (2013)
Diagnostic Interpretation of Array Data Using Public Databases and Internet Sources
Nicole de Leeuw et al.
HUMAN MUTATION (2012)
An integrated map of genetic variation from 1,092 human genomes
David M. Altshuler et al.
NATURE (2012)
An evidence-based approach to establish the functional and clinical significance of copy number variants in intellectual and developmental disabilities
Erin B. Kaminsky et al.
GENETICS IN MEDICINE (2011)
Consensus Statement: Chromosomal Microarray Is a First-Tier Clinical Diagnostic Test for Individuals with Developmental Disabilities or Congenital Anomalies
David T. Miller et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2010)
The clinical context of copy number variation in the human genome
Charles Lee et al.
EXPERT REVIEWS IN MOLECULAR MEDICINE (2010)
Origins and functional impact of copy number variation in the human genome
Donald F. Conrad et al.
NATURE (2010)
Public data archives for genomic structural variation
Deanna M. Church et al.
NATURE GENETICS (2010)
Discovery of common Asian copy number variants using integrated high-resolution array CGH and massively parallel DNA sequencing
Hansoo Park et al.
NATURE GENETICS (2010)
Towards a comprehensive structural variation map of an individual human genome
Andy W. Pang et al.
GENOME BIOLOGY (2010)
DECIPHER: Database of Chromosomal Imbalance and Phenotype in Humans Using Ensembl Resources
Helen V. Firth et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2009)
Challenges and standards in integrating surveys of structural variation
Stephen W. Scherer et al.
NATURE GENETICS (2007)
Structural variation in the human genome
L Feuk et al.
NATURE REVIEWS GENETICS (2006)
Development of bioinformatics resources for display and analysis of copy number and other structural variants in the human genome
J. Zhang et al.
CYTOGENETIC AND GENOME RESEARCH (2006)
The Sequence Ontology: a tool for the unification of genome annotations
K Eilbeck et al.
GENOME BIOLOGY (2005)
Detection of large-scale variation in the human genome
AJ Iafrate et al.
NATURE GENETICS (2004)
Large-scale copy number polymorphism in the human genome
J Sebat et al.
SCIENCE (2004)
The Generic Genome Browser: A building block for a model organism system database
LD Stein et al.
GENOME RESEARCH (2002)
Recent segmental duplications in the human genome
JA Bailey et al.
SCIENCE (2002)