A very fast and accurate method for calling aberrations in array-CGH data

被引:13
作者
Benelli, Matteo [1 ,2 ]
Marseglia, Giuseppina [2 ]
Nannetti, Genni
Paravidino, Roberta [3 ]
Zara, Federico [4 ]
Bricarelli, Franca Dagna [3 ]
Torricelli, Francesca [2 ]
Magi, Alberto [1 ,2 ]
机构
[1] Univ Florence, Diagnost Genet Unit, Azienda Osped Univ Careggi, Careggi Hosp,Dept Med & Surg Crit Care, I-50141 Florence, Italy
[2] Univ Florence, Ctr Study Complex Dynam, I-50019 Florence, Italy
[3] Ente Osped Osped Galliera, Genet Lab, I-16128 Genoa, Italy
[4] Univ Genoa, Muscular & Neurodegenerat Dis Unit, Inst Gaslini, I-16147 Genoa, Italy
关键词
array-CGH; Calling procedure; COPY NUMBER; SEGMENTATION;
D O I
10.1093/biostatistics/kxq008
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Array comparative genomic hybridization (aCGH) is a microarray technology that allows one to detect and map genomic alterations. The standard workflow of the aCGH data analysis consists of 2 steps: detecting the boundaries of the regions of changed copy number by means of a segmentation algorithm (break point identification) and then labeling each region as loss, neutral, or gain with a probabilistic framework (calling procedure). In this paper, we introduce a novel calling procedure based on a mixture of truncated normal distributions, named FastCall, that aims to give aberration probabilities to segmented aCGH data in a very fast and accurate way. Both on synthetic and real aCGH data, FastCall obtains excellent performances in terms of classification accuracy and running time.
引用
收藏
页码:515 / 518
页数:4
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