Building and evaluation of bioinformatic pipeline for determination of clonal profiles in myelodysplastic syndrome

Q3 Mathematics
D. Bug, A. Prikhodko, E. Bakin, A. Tishkov, N. Petukhova, I. Barkhatov, E. Morozova, I. Moiseev
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引用次数: 0

Abstract

Introduction: There is growing evidence of a connection between tumor clonal profile and its clinical impact. However, there is a lack of a feasible and reliable method for clonal profiling in actual clinical practice. Myelodysplastic syndrome is a clonal hematopoietic stem cell disorder characterized by morphological dysplasia, cytopenia and a high risk of evolution to acute myeloid leukemia. The clinical outcome of myelodysplastic syndrome is greatly heterogeneous; therefore, specific examination of clonal profiles is needed to resolve the prognosis of patients with such complex disorders. Purpose: Development of a pipeline specifically for determining the clonal profiles in patients with myelodysplastic syndrome on the basis of target next-generation sequencing data. Results: The pipeline was developed and evaluated on a set of 35 patients with high-risk myelodysplastic syndrome. It is possible to use the target sequencing data in order to assess the heterogeneity of clonal profiles and characterize their genetic features. This approach allows you to identify the consistency between a specific individual profile and the disease prognosis, which can be critical for the treatment decision. Herein, the characterization and analysis of clonal profiles are presented. Practical relevance: The information about relation patterns between clonal profile characteristics (number of subclones, mutations-per-clone rate) and clinical outcome can be used by doctors in current practice for a more accurate therapy selection depending on the identified individual specificity of the disease.
骨髓增生异常综合征克隆谱测定生物信息学管道的建立与评价
越来越多的证据表明肿瘤克隆谱与其临床影响之间存在联系。然而,在实际临床实践中缺乏一种可行可靠的克隆谱分析方法。骨髓增生异常综合征是一种克隆性造血干细胞疾病,其特征是形态发育异常、细胞减少和向急性髓系白血病发展的高风险。骨髓增生异常综合征的临床结果差异很大;因此,需要对克隆谱进行特异性检查,以解决此类复杂疾病患者的预后问题。目的:基于下一代目标测序数据,开发一种专门用于测定骨髓增生异常综合征患者克隆谱的管道。结果:该管道在35例高危骨髓增生异常综合征患者中开发和评估。有可能使用目标测序数据,以评估克隆谱的异质性和表征其遗传特征。这种方法使您能够确定特定个体特征与疾病预后之间的一致性,这对于治疗决策至关重要。本文对克隆谱进行了鉴定和分析。实际意义:有关克隆谱特征(亚克隆数量、每克隆突变率)与临床结果之间的关系模式的信息,可被医生在当前实践中用于更准确的治疗选择,这取决于已确定的疾病的个体特异性。
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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来源期刊
Informatsionno-Upravliaiushchie Sistemy
Informatsionno-Upravliaiushchie Sistemy Mathematics-Control and Optimization
CiteScore
1.40
自引率
0.00%
发文量
35
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