Computel: Computation of Mean Telomere Length from Whole-Genome Next-Generation Sequencing Data

被引:45
|
作者
Nersisyan, Lilit [1 ]
Arakelyan, Arsen [1 ]
机构
[1] Natl Acad Sci Republ Armenia, Inst Mol Biol, Grp Bioinformat, Yerevan, Armenia
来源
PLOS ONE | 2015年 / 10卷 / 04期
关键词
GENE-EXPRESSION; DNA; ALIGNMENT; DISEASE; CANCER; LONG; END;
D O I
10.1371/journal.pone.0125201
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Telomeres are the ends of eukaryotic chromosomes, consisting of consecutive short repeats that protect chromosome ends from degradation. Telomeres shorten with each cell division, leading to replicative cell senescence. Deregulation of telomere length homeostasis is associated with the development of various age-related diseases and cancers. A number of experimental techniques exist for telomere length measurement; however, until recently, the absence of tools for extracting telomere lengths from high-throughput sequencing data has significantly obscured the association of telomere length with molecular processes in normal and diseased conditions. We have developed Computel, a program in R for computing mean telomere length from whole-genome next-generation sequencing data. Computel is open source, and is freely available at https://github.com/lilit-nersisyan/computel. It utilizes a short-read alignment-based approach and integrates various popular tools for sequencing data analysis. We validated it with synthetic and experimental data, and compared its performance with the previously available software. The results have shown that Computel outperforms existing software in accuracy, independence of results from sequencing conditions, stability against inherent sequencing errors, and better ability to distinguish pure telomeric sequences from interstitial telomeric repeats. By providing a highly reliable methodology for determining telomere lengths from whole-genome sequencing data, Computel should help to elucidate the role of telomeres in cellular health and disease.
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页数:14
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