Literature DB >> 19948744

A shifting level model algorithm that identifies aberrations in array-CGH data.

Alberto Magi1, Matteo Benelli, Giuseppina Marseglia, Genni Nannetti, Maria Rosaria Scordo, Francesca Torricelli.   

Abstract

Array comparative genomic hybridization (aCGH) is a microarray technology that allows one to detect and map genomic alterations. The goal of aCGH analysis is to identify the boundaries of the regions where the number of DNA copies changes (breakpoint identification) and then to label each region as loss, neutral, or gain (calling). In this paper, we introduce a new algorithm, based on the shifting level model (SLM), with the aim of locating regions with different means of the log(2) ratio in genomic profiles obtained from aCGH data. We combine the SLM algorithm with the CGHcall calling procedure and compare their performances with 5 state-of-the-art methods. When dealing with synthetic data, our method outperforms the other 5 algorithms in detecting the change in the number of DNA copies in the most challenging situations. For real aCGH data, SLM is able to locate all the cytogenetically mapped aberrations giving a smaller number of false-positive breakpoints than the compared methods. The application of the SLM algorithm is not limited to aCGH data. Our approach can also be used for the analysis of several emerging experimental strategies such as high-resolution tiling array.

Mesh:

Year:  2009        PMID: 19948744     DOI: 10.1093/biostatistics/kxp051

Source DB:  PubMed          Journal:  Biostatistics        ISSN: 1465-4644            Impact factor:   5.899


  13 in total

1.  Genome-wide copy number analysis in pediatric glioblastoma multiforme.

Authors:  Laura Giunti; Marilena Pantaleo; Iacopo Sardi; Aldesia Provenzano; Alberto Magi; Stefania Cardellicchio; Francesca Castiglione; Lorenzo Tattini; Francesca Novara; Anna Maria Buccoliero; Maurizio de Martino; Lorenzo Genitori; Orsetta Zuffardi; Sabrina Giglio
Journal:  Am J Cancer Res       Date:  2014-05-26       Impact factor: 6.166

Review 2.  Statistical Considerations on NGS Data for Inferring Copy Number Variations.

Authors:  Jie Chen
Journal:  Methods Mol Biol       Date:  2021

3.  Enhanced copy number variants detection from whole-exome sequencing data using EXCAVATOR2.

Authors:  Romina D'Aurizio; Tommaso Pippucci; Lorenzo Tattini; Betti Giusti; Marco Pellegrini; Alberto Magi
Journal:  Nucleic Acids Res       Date:  2016-08-09       Impact factor: 16.971

4.  Detecting common copy number variants in high-throughput sequencing data by using JointSLM algorithm.

Authors:  Alberto Magi; Matteo Benelli; Seungtai Yoon; Franco Roviello; Francesca Torricelli
Journal:  Nucleic Acids Res       Date:  2011-02-14       Impact factor: 16.971

5.  Shall genomic correlation structure be considered in copy number variants detection?

Authors:  Fei Qin; Xizhi Luo; Guoshuai Cai; Feifei Xiao
Journal:  Brief Bioinform       Date:  2021-11-05       Impact factor: 13.994

Review 6.  Detection of Genomic Structural Variants from Next-Generation Sequencing Data.

Authors:  Lorenzo Tattini; Romina D'Aurizio; Alberto Magi
Journal:  Front Bioeng Biotechnol       Date:  2015-06-25

7.  EXCAVATOR: detecting copy number variants from whole-exome sequencing data.

Authors:  Alberto Magi; Lorenzo Tattini; Ingrid Cifola; Romina D'Aurizio; Matteo Benelli; Eleonora Mangano; Cristina Battaglia; Elena Bonora; Ants Kurg; Marco Seri; Pamela Magini; Betti Giusti; Giovanni Romeo; Tommaso Pippucci; Gianluca De Bellis; Rosanna Abbate; Gian Franco Gensini
Journal:  Genome Biol       Date:  2013       Impact factor: 13.583

8.  CloneCNA: detecting subclonal somatic copy number alterations in heterogeneous tumor samples from whole-exome sequencing data.

Authors:  Zhenhua Yu; Ao Li; Minghui Wang
Journal:  BMC Bioinformatics       Date:  2016-08-19       Impact factor: 3.169

9.  VEGAWES: variational segmentation on whole exome sequencing for copy number detection.

Authors:  Samreen Anjum; Sandro Morganella; Fulvio D'Angelo; Antonio Iavarone; Michele Ceccarelli
Journal:  BMC Bioinformatics       Date:  2015-09-29       Impact factor: 3.169

10.  PSCC: sensitive and reliable population-scale copy number variation detection method based on low coverage sequencing.

Authors:  Xuchao Li; Shengpei Chen; Weiwei Xie; Ida Vogel; Kwong Wai Choy; Fang Chen; Rikke Christensen; Chunlei Zhang; Huijuan Ge; Haojun Jiang; Chang Yu; Fang Huang; Wei Wang; Hui Jiang; Xiuqing Zhang
Journal:  PLoS One       Date:  2014-01-21       Impact factor: 3.240

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