Genome-wide copy number analysis using copy number inferring tool (CNIT) and DNA pooling

Human Mutation

Volumn 29, Issue 8, 2008, Pages 1055-1062

  Lin, Chien Hsing ^a   Huang, Mei Chu ^b   Li, Ng Hui ^c   Wu, Jer Yuarn ^c   Chen, Yuan Tsong ^c   Fann, Cathy S J ^a,c  

^a NATIONAL YANG MING UNIVERSITY   (Taiwan)

^b INSTITUTE OF STATISTICAL SCIENCE   (Taiwan)

^c INSTITUTE OF BIOMEDICAL SCIENCES   (Taiwan)

Author keywords

Chromosomal abnormality; CNIT; CNV; Copy number variations; DNA pooling; GeneChip; SNP genotyping

Indexed keywords

ALLELE; ARTICLE; COPY NUMBER INFERRING TOOL; COPY NUMBER VARIATION; DIAGNOSTIC ACCURACY; DNA MICROARRAY; FALSE NEGATIVE RESULT; GENE AMPLIFICATION; GENE DELETION; GENE POOL; GENETIC ALGORITHM; GENETIC VARIABILITY; HIDDEN MARKOV MODEL; HUMAN; PRIORITY JOURNAL; SENSITIVITY ANALYSIS; SINGLE NUCLEOTIDE POLYMORPHISM;

GENE DOSAGE; GENOME, HUMAN; HUMANS; MARKOV CHAINS; OLIGONUCLEOTIDE ARRAY SEQUENCE ANALYSIS; POLYMORPHISM, SINGLE NUCLEOTIDE; SENSITIVITY AND SPECIFICITY; SOFTWARE;

EID: 49149091178     PISSN: 10597794     EISSN: None     Source Type: Journal    
DOI: 10.1002/humu.20760     Document Type: Article

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