A hidden Markov model-based approach to reconstructing double minute chromosome amplicons

Ruslan T. Mardugalliamov, K. Nasr, Matthew Hayes
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引用次数: 1

Abstract

Double minute chromosomes (DMs) are circular fragments of extrachromosomal DNA. They cause extreme gene amplification in the cells of malignant tumours. Their existence correlates with malignant tumour cell behaviour and drug resistance. Locating DMs is important for informing precision therapy to cancer treatment. Furthermore, accurate detection of double minutes requires precise reconstruction of their amplicons, which are the highly-amplified gene-carrying contiguous segments that adjoin to form DMs. This work presents AmpliconFinder - a Hidden-Markov Model-based approach to detect DM amplicons. To assess its efficacy, AmpliconFinder was used to augment an earlier framework for DM detection (DMFinder), thus improving its sensitivity and robustness to noisy sequence data. Experiments on simulated genomic data show that augmenting DMFinder with AmpliconFinder significantly increased the sensitivity of DMFinder on these data. Moreover, DMFinder with AmpliconFinder found all previously reported DMs in three pediatric medulloblastoma datasets, whereas the original DMFinder framework found none.
基于隐马尔可夫模型的双分钟染色体扩增子重构方法
双分钟染色体(DMs)是染色体外DNA的环状片段。它们在恶性肿瘤细胞中引起极端的基因扩增。它们的存在与恶性肿瘤细胞的行为和耐药性有关。定位dm对于癌症治疗的精准治疗具有重要意义。此外,双分钟的准确检测需要精确重建其扩增子,这些扩增子是高度扩增的携带基因的连续片段,相邻形成dm。这项工作提出了AmpliconFinder -一种基于隐马尔可夫模型的方法来检测DM放大器。为了评估其有效性,使用AmpliconFinder来增强早期DM检测框架(DMFinder),从而提高其对噪声序列数据的灵敏度和鲁棒性。模拟基因组数据的实验表明,用AmpliconFinder增强DMFinder可以显著提高DMFinder对这些数据的灵敏度。此外,使用AmpliconFinder的DMFinder在三个儿童成神经管细胞瘤数据集中发现了所有先前报道的dm,而原始的DMFinder框架没有发现。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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