Comparative analysis of whole genome sequencing-based telomere length measurement techniques

被引:37
|
作者
Lee, Michael [1 ]
Napier, Christine E. [2 ]
Yang, Sile F. [1 ]
Arthur, Jonathan W. [3 ]
Reddel, Roger R. [2 ]
Pickett, Hilda A. [1 ]
机构
[1] Univ Sydney, Childrens Med Res Inst, Telomere Length Regulat Grp, Westmead, NSW, Australia
[2] Univ Sydney, Canc Res Unit, Childrens Med Res Inst, Westmead, NSW, Australia
[3] Univ Sydney, Bioinformat Unit, Childrens Med Res Inst, Westmead, NSW, Australia
关键词
Telomere length; WGS; Motif_counter; TelSeq; Computel; qMotif; HUMAN-CELLS; MAMMALIAN TELOMERES; HUMAN-CHROMOSOMES; VARIANT REPEATS; HEALTHY-ADULTS; OLDER-PEOPLE; ASSOCIATION; FIBROBLASTS; DISEASE; MAINTENANCE;
D O I
10.1016/j.ymeth.2016.08.008
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Telomeres are regions of repetitive DNA at the ends of human chromosomes that function to maintain the integrity of the genome. Telomere attrition is associated with cellular ageing, whilst telomere maintenance is a prerequisite for malignant transformation. Whole genome sequencing (WGS) captures sequence information from the entire genome, including the telomeres, and is increasingly being applied in research and in the clinic. Several bioinformatics tools have been designed to determine telomere content and length from WGS data, and include Motif counter, TelSeq, Computel, qMotif, and Telomerecat. These tools utilise different approaches to identify, quantify and normalise telomeric reads; however, it is not known how they compare to one another. Here we describe the details and utility of each tool, and directly compare WGS telomere length output with laboratory-based telomere length measurements. In addition, we evaluate the accessibility, practicality, speed, and additional features of each tool. Each tool was tested using a range of telomere read extraction criteria, to determine the optimal parameters for the specific WGS read length. The aim of this article is to improve the accessibility of WGS telomere length measurement tools, which have the potential to be applied to WGS cohorts for clinical as well as research benefit. (C) 2016 Elsevier Inc. All rights reserved.
引用
下载
收藏
页码:4 / 15
页数:12
相关论文
共 50 条
  • [31] Systematic Comparison of Computational Tools for Sanger Sequencing-Based Genome Editing Analysis
    Aoki, Kanae
    Yamasaki, Mai
    Umezono, Riku
    Hamamoto, Takanori
    Kamachi, Yusuke
    CELLS, 2024, 13 (03)
  • [32] Genome sequencing-based transcriptomic analysis reveals novel genes in Peucedanum praeruptorum
    Cheng Song
    Yingyu Zhang
    Yunpeng Zhang
    Shanyong Yi
    Haoyu Pan
    Ranran Liao
    Yuanyuan Wang
    Bangxing Han
    BMC Genomic Data, 24
  • [33] Whole-genome sequencing-based analysis of Brucella species isolated from ruminants in various regions of Türki̇ye
    Songül Ötkün
    Sevil Erdenliğ Gürbi̇lek
    BMC Infectious Diseases, 24 (1)
  • [34] Whole Genome Sequencing-Based Molecular Epidemiologic Analysis of Autochthonous Dengue Virus Type 1 Strains Circulating in Japan in 2014
    Tajima, Shigeru
    Nakayama, Eri
    Kotaki, Akira
    Moi, Meng Ling
    Ikeda, Makiko
    Yagasaki, Kazumi
    Saito, Yuka
    Shibasaki, Ken-ichi
    Saijo, Masayuki
    Takasaki, Tomohiko
    JAPANESE JOURNAL OF INFECTIOUS DISEASES, 2017, 70 (01) : 45 - 49
  • [35] Whole-Genome Sequencing-Based Characterization of Listeria monocytogenes from Food and Animal Clinical Cases
    Aslantas, Ozkan
    Buyukaltay, Kaan
    Keskin, Oktay
    Gullu Yucetepe, Ayfer
    Adiguzel, Adem
    KAFKAS UNIVERSITESI VETERINER FAKULTESI DERGISI, 2023, 29 (03) : 221 - 230
  • [36] Whole-genome sequencing-based analyses of drug-resistant Mycobacterium tuberculosis from Taiwan
    Yu-Xin Xiao
    Kuang-Hung Liu
    Wan-Hsuan Lin
    Tai-Hua Chan
    Ruwen Jou
    Scientific Reports, 13
  • [37] Whole Genome Sequencing-Based Tracing of a 2022 Introduction and Outbreak of Xanthomonas hortorum pv. pelargonii
    Iruegas-Bocardo, Fernanda
    Weisberg, Alexandra J. J.
    Riutta, Elizabeth R. R.
    Kilday, Kameron
    Bonkowski, John C. C.
    Creswell, Tom
    Daughtrey, Margery L. L.
    Rane, Karen
    Grunwald, Niklaus J. J.
    Chang, Jeff H. H.
    Putnam, Melodie L. L.
    PHYTOPATHOLOGY, 2023, 113 (06) : 975 - 984
  • [38] A multicenter evaluation of a low pass whole genome sequencing-based solution for homologous recombination deficiency detection
    Buisson, A.
    Saintigny, P.
    Pujade-Lauraine, E.
    Grillot, C. Montoto
    Varcica, D.
    Barberis, M.
    Colombo, N.
    Harle, A.
    Gilson, P.
    Roma, C.
    Bergantino, F.
    Harter, P.
    Pignata, S.
    Martin, A. J. Gonzalez
    Schauer, C.
    Fujiwara, K.
    Vergote, I. B.
    Juhler-Nottrup, T. J.
    Just, P-A.
    Ray-Coquard, I. L.
    ANNALS OF ONCOLOGY, 2022, 33 (07) : S811 - S812
  • [39] Resetting the bar: Statistical significance in whole-genome sequencing-based association studies of global populations
    Pulit, Sara L.
    de With, Sera A. J.
    de Bakker, Paul I. W.
    GENETIC EPIDEMIOLOGY, 2017, 41 (02) : 145 - 151
  • [40] Whole-genome sequencing-based analyses of drug-resistant Mycobacterium tuberculosis from Taiwan
    Xiao, Yu-Xin
    Liu, Kuang-Hung
    Lin, Wan-Hsuan
    Chan, Tai-Hua
    Jou, Ruwen
    SCIENTIFIC REPORTS, 2023, 13 (01)