Literature DB >> 25595567

CNV-ROC: A cost effective, computer-aided analytical performance evaluator of chromosomal microarrays.

Corey W Goodman1, Heather J Major2, William D Walls3, Val C Sheffield4, Thomas L Casavant5, Benjamin W Darbro6.   

Abstract

Chromosomal microarrays (CMAs) are routinely used in both research and clinical laboratories; yet, little attention has been given to the estimation of genome-wide true and false negatives during the assessment of these assays and how such information could be used to calibrate various algorithmic metrics to improve performance. Low-throughput, locus-specific methods such as fluorescence in situ hybridization (FISH), quantitative PCR (qPCR), or multiplex ligation-dependent probe amplification (MLPA) preclude rigorous calibration of various metrics used by copy number variant (CNV) detection algorithms. To aid this task, we have established a comparative methodology, CNV-ROC, which is capable of performing a high throughput, low cost, analysis of CMAs that takes into consideration genome-wide true and false negatives. CNV-ROC uses a higher resolution microarray to confirm calls from a lower resolution microarray and provides for a true measure of genome-wide performance metrics at the resolution offered by microarray testing. CNV-ROC also provides for a very precise comparison of CNV calls between two microarray platforms without the need to establish an arbitrary degree of overlap. Comparison of CNVs across microarrays is done on a per-probe basis and receiver operator characteristic (ROC) analysis is used to calibrate algorithmic metrics, such as log2 ratio threshold, to enhance CNV calling performance. CNV-ROC addresses a critical and consistently overlooked aspect of analytical assessments of genome-wide techniques like CMAs which is the measurement and use of genome-wide true and false negative data for the calculation of performance metrics and comparison of CNV profiles between different microarray experiments.
Copyright © 2015 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Microarray; Precision; ROC; Sensitivity; Specificity

Mesh:

Substances:

Year:  2015        PMID: 25595567      PMCID: PMC4936396          DOI: 10.1016/j.jbi.2015.01.001

Source DB:  PubMed          Journal:  J Biomed Inform        ISSN: 1532-0464            Impact factor:   6.317


  15 in total

Review 1.  Microarray-based genomic DNA profiling technologies in clinical molecular diagnostics.

Authors:  Yiping Shen; Bai-Lin Wu
Journal:  Clin Chem       Date:  2009-02-20       Impact factor: 8.327

2.  Validation of a next-generation sequencing assay for clinical molecular oncology.

Authors:  Catherine E Cottrell; Hussam Al-Kateb; Andrew J Bredemeyer; Eric J Duncavage; David H Spencer; Haley J Abel; Christina M Lockwood; Ian S Hagemann; Stephanie M O'Guin; Lauren C Burcea; Christopher S Sawyer; Dayna M Oschwald; Jennifer L Stratman; Dorie A Sher; Mark R Johnson; Justin T Brown; Paul F Cliften; Bijoy George; Leslie D McIntosh; Savita Shrivastava; Tudung T Nguyen; Jacqueline E Payton; Mark A Watson; Seth D Crosby; Richard D Head; Robi D Mitra; Rakesh Nagarajan; Shashikant Kulkarni; Karen Seibert; Herbert W Virgin; Jeffrey Milbrandt; John D Pfeifer
Journal:  J Mol Diagn       Date:  2013-11-06       Impact factor: 5.568

3.  Two-sided confidence intervals for the single proportion: comparison of seven methods.

Authors:  R G Newcombe
Journal:  Stat Med       Date:  1998-04-30       Impact factor: 2.373

4.  Comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variants.

Authors:  Dalila Pinto; Katayoon Darvishi; Xinghua Shi; Diana Rajan; Diane Rigler; Tom Fitzgerald; Anath C Lionel; Bhooma Thiruvahindrapuram; Jeffrey R Macdonald; Ryan Mills; Aparna Prasad; Kristin Noonan; Susan Gribble; Elena Prigmore; Patricia K Donahoe; Richard S Smith; Ji Hyeon Park; Matthew E Hurles; Nigel P Carter; Charles Lee; Stephen W Scherer; Lars Feuk
Journal:  Nat Biotechnol       Date:  2011-05-08       Impact factor: 54.908

5.  American College of Medical Genetics recommendations for the design and performance expectations for clinical genomic copy number microarrays intended for use in the postnatal setting for detection of constitutional abnormalities.

Authors:  Hutton M Kearney; Sarah T South; Daynna J Wolff; Allen Lamb; Ada Hamosh; Kathleen W Rao
Journal:  Genet Med       Date:  2011-07       Impact factor: 8.822

6.  Origins and functional impact of copy number variation in the human genome.

Authors:  Donald F Conrad; Dalila Pinto; Richard Redon; Lars Feuk; Omer Gokcumen; Yujun Zhang; Jan Aerts; T Daniel Andrews; Chris Barnes; Peter Campbell; Tomas Fitzgerald; Min Hu; Chun Hwa Ihm; Kati Kristiansson; Daniel G Macarthur; Jeffrey R Macdonald; Ifejinelo Onyiah; Andy Wing Chun Pang; Sam Robson; Kathy Stirrups; Armand Valsesia; Klaudia Walter; John Wei; Chris Tyler-Smith; Nigel P Carter; Charles Lee; Stephen W Scherer; Matthew E Hurles
Journal:  Nature       Date:  2009-10-07       Impact factor: 49.962

7.  Array analysis and karyotyping: workflow consequences based on a retrospective study of 36,325 patients with idiopathic developmental delay in the Netherlands.

Authors:  Ron Hochstenbach; Ellen van Binsbergen; John Engelen; Aggie Nieuwint; Abeltje Polstra; Pino Poddighe; Claudia Ruivenkamp; Birgit Sikkema-Raddatz; Dominique Smeets; Martin Poot
Journal:  Eur J Med Genet       Date:  2009-04-09       Impact factor: 2.708

8.  Chromosomal microarray testing influences medical management.

Authors:  Michael E Coulter; David T Miller; David J Harris; Pamela Hawley; Jonathan Picker; Amy E Roberts; Magdi M Sobeih; Mira Irons
Journal:  Genet Med       Date:  2011-09       Impact factor: 8.822

9.  A study of CNVs as trait-associated polymorphisms and as expression quantitative trait loci.

Authors:  Eric R Gamazon; Dan L Nicolae; Nancy J Cox
Journal:  PLoS Genet       Date:  2011-02-03       Impact factor: 5.917

10.  Clinical genetic testing for patients with autism spectrum disorders.

Authors:  Yiping Shen; Kira A Dies; Ingrid A Holm; Carolyn Bridgemohan; Magdi M Sobeih; Elizabeth B Caronna; Karen J Miller; Jean A Frazier; Iris Silverstein; Jonathan Picker; Laura Weissman; Peter Raffalli; Shafali Jeste; Laurie A Demmer; Heather K Peters; Stephanie J Brewster; Sara J Kowalczyk; Beth Rosen-Sheidley; Caroline McGowan; Andrew W Duda; Sharyn A Lincoln; Kathryn R Lowe; Alison Schonwald; Michael Robbins; Fuki Hisama; Robert Wolff; Ronald Becker; Ramzi Nasir; David K Urion; Jeff M Milunsky; Leonard Rappaport; James F Gusella; Christopher A Walsh; Bai-Lin Wu; David T Miller
Journal:  Pediatrics       Date:  2010-03-15       Impact factor: 7.124

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