Statistical model for whole genome sequencing and its application to minimally invasive diagnosis of fetal genetic disease

Bioinformatics

Volumn 25, Issue 10, 2009, Pages 1244-1250

  Chu, Tianjiao ^a,b   Bunce, Kimberly ^a,b   Hogge, Allen W ^a,b   Peters, David G ^a,b  

^a UNIVERSITY OF PITTSBURGH SCHOOL OF MEDICINE   (United States)

^b UNIVERSITY OF PITTSBURGH   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DNA;

ADULT; ARTICLE; CASE REPORT; CHILD; DIAGNOSTIC ACCURACY; DNA EXTRACTION; DNA SEQUENCE; FEMALE; FETUS DISEASE; FETUS KARYOTYPING; FIRST TRIMESTER PREGNANCY; GENETIC DISORDER; HUMAN; MALE; MATERNAL PLASMA; MINIMALLY INVASIVE PROCEDURE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SENSITIVITY AND SPECIFICITY; SEQUENCE ANALYSIS; STATISTICAL MODEL; TRISOMY 21;

ADULT; CHILD, PRESCHOOL; DNA; DOWN SYNDROME; FEMALE; FETAL DISEASES; FETUS; GENOME, HUMAN; HUMANS; MALE; MODELS, STATISTICAL; PREGNANCY; PREGNANCY TRIMESTER, FIRST; PRENATAL DIAGNOSIS; SEQUENCE ANALYSIS, DNA;

EID: 65549102180     PISSN: 13674803     EISSN: 14602059     Source Type: Journal    
DOI: 10.1093/bioinformatics/btp156     Document Type: Article

References (14)

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