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DNAfusion:一个用于提高液体活检中基因融合检测灵敏度的 R/Bioconductor 包。

DNAfusion: an R/Bioconductor package for increased sensitivity of detecting gene fusions in liquid biopsies.

机构信息

Department of Clinical Biochemistry, Faculty of Health, Aarhus University Hospital, Palle Juul-Jensens Boulevard 69, 8200, Århus N, Denmark.

Department of Clinical Medicine, Aarhus University, Århus N, Denmark.

出版信息

BMC Bioinformatics. 2023 Apr 4;24(1):131. doi: 10.1186/s12859-023-05259-3.

Abstract

BACKGROUND

EML4-ALK gene fusions are oncogenic drivers in non-small cell lung cancer (NSCLC), and liquid biopsies containing EML4-ALK fragments can be used to study tumor dynamics using next-generation sequencing (NGS). However, the sensitivity of EML4-ALK detection varies between pipelines and analysis tools.

RESULTS

We developed an R/Bioconductor package, DNAfusion, which can be applied to BAM files generated by commercially available NGS pipelines, such as AVENIO. Forty-eight blood samples from a training cohort consisting of 41 stage IV EML4-ALK-positive NSCLC patients and seven healthy controls were used to develop DNAfusion. DNAfusion detected EML4-ALK in significantly more samples (sensitivity = 61.0%) compared to AVENIO (sensitivity = 36.6%). The newly identified EML4-ALK-positive patients were verified using droplet digital PCR. DNAfusion was subsequently validated in a blinded validation cohort comprising 24 EML4-ALK-positive and 24 EML4-ALK-negative stage IV NSCLC patients. DNAfusion detected significantly more EML4-ALK individuals in the validation cohort (sensitivity = 62.5%) compared to AVENIO (sensitivity = 29.2%). DNAfusion demonstrated a specificity of 100% in both the training and validation cohorts.

CONCLUSION

Here we present DNAfusion, which increases the sensitivity of EML4-ALK detection in liquid biopsies and can be implemented downstream of commercially available NGS pipelines. The simplistic method of operating the R package makes it easy to implement in the clinical setting, enabling wider expansion of NGS-based diagnostics.

摘要

背景

EML4-ALK 基因融合是非小细胞肺癌(NSCLC)的致癌驱动因素,含有 EML4-ALK 片段的液体活检可用于使用下一代测序(NGS)研究肿瘤动态。然而,不同的管道和分析工具对 EML4-ALK 的检测灵敏度不同。

结果

我们开发了一个 R/Bioconductor 包 DNAfusion,可应用于 AVENIO 等市售 NGS 管道生成的 BAM 文件。从一个包含 41 名 EML4-ALK 阳性 IV 期 NSCLC 患者和 7 名健康对照者的训练队列的 48 个血液样本中开发了 DNAfusion。与 AVENIO(灵敏度=36.6%)相比,DNAfusion 检测到 EML4-ALK 的样本数显著更多(灵敏度=61.0%)。使用液滴数字 PCR 对新发现的 EML4-ALK 阳性患者进行了验证。随后在一个包含 24 名 EML4-ALK 阳性和 24 名 EML4-ALK 阴性 IV 期 NSCLC 患者的盲法验证队列中验证了 DNAfusion。与 AVENIO(灵敏度=29.2%)相比,DNAfusion 在验证队列中检测到的 EML4-ALK 个体显著更多(灵敏度=62.5%)。DNAfusion 在训练和验证队列中的特异性均为 100%。

结论

在这里,我们介绍了 DNAfusion,它提高了液体活检中 EML4-ALK 的检测灵敏度,并可在市售 NGS 管道下游实施。R 包的操作方法简单,易于在临床环境中实施,从而可以更广泛地扩展基于 NGS 的诊断。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e45/10074784/ea299714ee6e/12859_2023_5259_Fig1_HTML.jpg

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