Defining the impact of maternal cell contamination on the interpretation of prenatal microarray analysis

To understand the ability of microarray-based comparative genomic hybridization to detect copy-number variation in the presence of maternal cell contamination. To simulate maternal cell contamination, normal female DNA was mixed at various levels with DNA carrying known copy-number variations. Mixtu...

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Bibliographic Details
Published in:Genetics in medicine 2012-11, Vol.14 (11), p.914-921
Main Authors: Lamb, Allen N, Rosenfeld, Jill A, Coppinger, Justine, Dodge, Erin T, Dabell, Mindy Preston, Torchia, Beth S, Ravnan, J Britt, Shaffer, Lisa G, Ballif, Blake C
Format: Article
Language:English
Subjects:
Algorithms
Amniotic Fluid - cytology
Cells, Cultured
Comparative Genomic Hybridization - methods
Computer Simulation
Decidua - cytology
DNA Copy Number Variations
Female
Fetus - cytology
Genome, Human
Humans
Male
Oligonucleotide Array Sequence Analysis - methods
Pregnancy
Prenatal Diagnosis - methods
Reproducibility of Results
Sensitivity and Specificity
Sequence Analysis, DNA - methods
Sex chromosomes
Sex Chromosomes - genetics
Software
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Summary:To understand the ability of microarray-based comparative genomic hybridization to detect copy-number variation in the presence of maternal cell contamination. To simulate maternal cell contamination, normal female DNA was mixed at various levels with DNA carrying known copy-number variations. Mixtures were run on a whole-genome 135K oligonucleotide-based array. Data were analyzed with custom analysis software. The array and software design allowed detection of larger copy-number variations at higher levels of maternal cell contamination than smaller copy-number variations. The smallest duplications and deletions were obscured at 22-31% and 55-58% maternal cell contamination, respectively. With male fetal samples, the sex chromosome ratios started showing observable shifts at ~10% maternal cell contamination. As knowledge of the maternal cell contamination level aids in interpretation of array results, we recommend concurrent, independent maternal cell contamination studies for all fetal samples for accurate and timely results. With male fetal samples in our laboratory, interfering levels of maternal cell contamination can be excluded when the sex chromosome plots appear normal. Thus, reportable male microarray-based comparative genomic hybridization results may be occasionally achieved without maternal cell contamination studies. Because the effects of maternal cell contamination on microarray results are dependent on array platforms, experimental techniques, and software algorithms, each laboratory should perform its own analysis to determine acceptable levels of maternal cell contamination for its assays.
ISSN:1098-3600
1530-0366
DOI:10.1038/gim.2012.77