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特百惠:使用 RNA-seq 检测癌症中的外显子缺失事件。

Toblerone: detecting exon deletion events in cancer using RNA-seq.

机构信息

Sir Peter MacCallum Department of Oncology, University of Melbourne, Parkville, VIC, 3010, Australia.

Murdoch Children's Research Institute, Parkville, VIC, 3052, Australia.

出版信息

F1000Res. 2023 Feb 3;12:130. doi: 10.12688/f1000research.129490.1. eCollection 2023.

Abstract

Cancer is driven by mutations of the genome that can result in the activation of oncogenes or repression of tumour suppressor genes. In acute lymphoblastic leukemia (ALL) focal deletions in IKAROS family zinc finger 1 (IKZF1) result in the loss of zinc-finger DNA-binding domains and a dominant negative isoform that is associated with higher rates of relapse and  poorer patient outcomes. Clinically, the presence of IKZF1 deletions informs prognosis and treatment options. In this work we developed a method for detecting exon deletions in genes using RNA-seq with application to IKZF1. We developed a pipeline that first uses a custom transcriptome reference consisting of transcripts with exon deletions.  Next, RNA-seq reads are mapped using a pseudoalignment algorithm to identify reads that uniquely support deletions. These are then evaluated for evidence of the deletion with respect to gene expression and other samples. We applied the algorithm, named Toblerone, to a cohort of 99 B-ALL paediatric samples including validated IKZF1 deletions. Furthermore, we developed a graphical desktop app for non-bioinformatics users that can quickly and easily identify and report deletions in IKZF1 from RNA-seq data with informative graphical outputs.

摘要

癌症是由基因组突变驱动的,这些突变可能导致癌基因的激活或肿瘤抑制基因的失活。在急性淋巴细胞白血病 (ALL) 中,IKAROS 家族锌指蛋白 1 (IKZF1) 的焦点缺失导致锌指 DNA 结合结构域的丢失和显性负性异构体的产生,与更高的复发率和更差的患者预后相关。临床上,IKZF1 缺失的存在提示预后和治疗选择。在这项工作中,我们开发了一种使用 RNA-seq 检测基因中外显子缺失的方法,并将其应用于 IKZF1。我们开发了一个管道,首先使用包含外显子缺失的转录本的自定义转录组参考。然后,使用伪比对算法将 RNA-seq 读取映射到唯一支持缺失的读取。然后,根据基因表达和其他样本评估这些缺失的证据。我们将名为 Toblerone 的算法应用于包括经过验证的 IKZF1 缺失在内的 99 例儿科 B-ALL 样本队列中。此外,我们为非生物信息学用户开发了一个图形桌面应用程序,该应用程序可以快速、轻松地从 RNA-seq 数据中识别和报告 IKZF1 的缺失,并提供有信息的图形输出。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e772/10521068/862052311564/f1000research-12-142177-g0000.jpg

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