Meet the author: Jayne Hehir-Kwa.

IF 11.1 Q1 CELL BIOLOGY Cell genomics Pub Date : 2024-11-13 DOI:10.1016/j.xgen.2024.100694
Jayne Hehir-Kwa
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引用次数: 0

Abstract

Jayne Hehir-Kwa is based at the Princess Máxima Center for Pediatric Oncology in the Netherlands and is an associate group leader within the Kemmeren group and the Big Data Core. Her work is focused on genomic and transcriptomic sequencing of pediatric cancer and the resulting analysis, storage, and management of this large volume of valuable patient data. In this issue of Cell Genomics, her team presents the research article "Complex structural variation is prevalent and highly pathogenic in pediatric solid tumors," which illustrates complex genomic rearrangements in five pediatric cancer types.

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认识作者杰恩-海尔-夸(Jayne Hehir-Kwa)。
Jayne Hehir-Kwa 在荷兰的马克西马公主儿科肿瘤中心工作,是 Kemmeren 小组和大数据核心的副组长。她的工作重点是儿科癌症的基因组和转录组测序,以及由此产生的大量宝贵患者数据的分析、存储和管理。在本期《细胞基因组学》(Cell Genomics)杂志上,她的团队发表了研究文章《复杂结构变异在小儿实体瘤中普遍存在并具有高度致病性》(Complex structural variation is prevalent and highly pathogenic in pediatric solid tumors),文章展示了五种小儿癌症类型的复杂基因组重排。
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
CiteScore
7.10
自引率
0.00%
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0
期刊最新文献
A combined deep learning framework for mammalian m6A site prediction. Analysis of single-cell CRISPR perturbations indicates that enhancers predominantly act multiplicatively. Complex structural variation is prevalent and highly pathogenic in pediatric solid tumors. Gene regulatory network inference from CRISPR perturbations in primary CD4+ T cells elucidates the genomic basis of immune disease. Leveraging genomes to support conservation and bioeconomy policies in a megadiverse country.
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