Representational Oligonucleotide Microarray Analysis (ROMA) and comparison of binning and change-point methods of analysis: Application to detection of del22q11.2 (DiGeorge) syndrome

Human Mutation

Volumn 29, Issue 1, 2008, Pages 176-181

  Stanczak, Christopher M ^a   Chen, Zugen ^a   Nelson, Stanley F ^a   Suchard, Marc ^a,d   McCabe, Edward R B ^a,b,c   McGhee, Sean A ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

^b MATTEL CHILDREN S HOSPITAL   (United States)

^c UNIVERSITY OF CALIFORNIA   (United States)

^d UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

Array; Cytogenetic analysis; DiGeorge Syndrome; Microarray analysis; Newborn screening; Representational oligonucleotide; ROMA; SNP

Indexed keywords

GENOMIC DNA;

ACCURACY; ALGORITHM; ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; BINNING; CASE REPORT; CELL LINE; CHANGE POINT MODEL ALGORITHM; CHROMOSOME 22Q; CHROMOSOME ANALYSIS; DATA ANALYSIS; DIGEORGE SYNDROME; DNA ISOLATION; DNA MICROARRAY; FALSE POSITIVE RESULT; HUMAN; HUMAN CELL; INFANT; MALE; NEWBORN SCREENING; PRIORITY JOURNAL; REPRESENTATIONAL OLIGONUCLEOTIDE MICROARRAY ANALYSIS;

ALGORITHMS; CELL LINE; CHROMOSOMES, HUMAN, PAIR 22; DIGEORGE SYNDROME; DNA; GENE DELETION; GENE DOSAGE; HUMANS; INFANT; MALE; OLIGONUCLEOTIDE ARRAY SEQUENCE ANALYSIS;

EID: 38149041668     PISSN: 10597794     EISSN: None     Source Type: Journal    
DOI: 10.1002/humu.20593     Document Type: Article

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