DERIVING CHEMOSENSITIVITY FROM CELL LINES: FORENSIC BIOINFORMATICS AND REPRODUCIBLE RESEARCH IN HIGH-THROUGHPUT BIOLOGY

被引:175
作者
Baggerly, Keith A. [1 ]
Coombes, Kevin R. [1 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Bioinformat & Computat Biol, Houston, TX 77030 USA
关键词
Microarrays; reproducibility; forensic bioinformatics; RETRACTED ARTICLE. SEE; PATTERNS; SERUM; MICROARRAYS; PREDICTION; RESISTANCE;
D O I
10.1214/09-AOAS291
中图分类号
O21 [概率论与数理统计]; C8 [统计学];
学科分类号
020208 ; 070103 ; 0714 ;
摘要
High-throughput biological assays such as microarrays let us ask very detailed questions about how diseases operate, and promise to let us personalize therapy. Data processing, however, is often not described well enough to allow for exact reproduction of the results, leading to exercises in "forensic bioinformatics" where aspects of raw data and reported results are used to infer what methods must have been employed. Unfortunately, poor documentation can shift from an inconvenience to an active danger when it obscures not just methods but errors. In this report we examine several related papers purporting to use microarray-based signatures of drug sensitivity derived from cell lines to predict patient response. Patients in clinical trials are currently being allocated to treatment arms on the basis of these results. However, we show in five case studies that the results incorporate several simple errors that may be potting patients at risk. One theme that emerges is that the most common errors are simple (e.g., row or column offsets); conversely, it is our experience that the most simple errors are common. We then discuss steps we are taking to avoid such errors in our own investigations.
引用
收藏
页码:1309 / 1334
页数:26
相关论文
共 34 条
[1]   RETRACTED: Genomic and Molecular Profiling Predicts Response to Temozolomide in Melanoma (Retracted Article. See vol 15, pg 3240, 2009) [J].
Augustine, Christina K. ;
Yoo, Jin Soo ;
Potti, Anil ;
Yoshimoto, Yasunori ;
Zipfel, Patricia A. ;
Friedman, Henry S. ;
Nevins, Joseph R. ;
Ali-Osman, Francis ;
Tyler, Douglas S. .
CLINICAL CANCER RESEARCH, 2009, 15 (02) :502-510
[2]   Signal in noise: Evaluating reported reproducibility of serum proteomic tests for ovarian cancer [J].
Baggerly, KA ;
Morris, JS ;
Edmonson, SR ;
Coombes, KR .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2005, 97 (04) :307-309
[3]  
Baggerly KA, 2004, ENDOCR-RELAT CANCER, V11, P583, DOI 10.1677/erc.1.00868
[4]   Reproducibility of SELDI-TOF protein patterns in serum: comparing datasets from different experiments [J].
Baggerly, KA ;
Morris, JS ;
Coombes, KR .
BIOINFORMATICS, 2004, 20 (05) :777-U710
[5]  
BAGGERLY KA, 2009, EXAMINING DOCETAXE S, V5, DOI DOI 10.1214/09-AOAS291SUPPE
[6]  
BAGGERLY KA, 2009, CISPLATIN PEMETREX S, V2, DOI DOI 10.1214/09-AOAS291SUPPB
[7]  
BAGGERLY KA, 2009, SURVEYING CELL LIN S, V4, DOI DOI 10.1214/09-AOAS291SUPPD
[8]  
BAGGERLY KA, 2009, EXAMINING DOXORUBI S, V1, DOI DOI 10.1214/09-AOAS291SUPPA
[9]  
BAGGERLY KA, 2009, EXAMINING COMBINAT S, V3, DOI DOI 10.1214/09-AOAS291SUPPC
[10]   Run batch effects potentially compromise the usefulness of genomic signatures for ovarian cancer [J].
Baggerly, Keith A. ;
Coombes, Kevin R. ;
Neeley, E. Shannon .
JOURNAL OF CLINICAL ONCOLOGY, 2008, 26 (07) :1186-1187