解析肿瘤异质性：通过形态学上不同细胞的低模板分析鉴定参与脊索瘤细胞发育的基因

资源简介

解析肿瘤异质性：通过形态学上不同细胞的低模板分析鉴定参与脊索瘤细胞发育的基因

【数据集背景】

本数据集源站标题为《Resolving Tumor Heterogeneity: Genes Involved in Chordoma Cell Development Identified by Low-Template Analysis of Morphologically Distinct Cells》。配套论文《Resolving Tumor Heterogeneity: Genes Involved in Chordoma Cell Development Identified by Low-Template Analysis of Morphologically Distinct Cells》发表于 PLoS ONE（2014），DOI：10.1371/journal.pone.0087663。源站首次发布：2014-02-04。

【数据内容】

源站原始描述：The classical sacrococcygeal chordoma tumor presents with a typical morphology of lobulated myxoid tumor tissue with cords, strands and nests of tumor cells. The population of cells consists of small non-vacuolated cells, intermediate cells with a wide range of vacuolization and large heavily vacuolated (physaliferous) cells. To date analysis was only performed on bulk tumor mass because of its rare incidence, lack of suited model systems and technical limitations thereby neglecting its heteroge…

【数据结构与技术规格】

文件数 4 个，合计 9.98 MB。Table_S1.xls：application/vnd.ms-excel，50.69 KB。Table_S2.xls：application/vnd.ms-excel，93.70 KB。Table_S3.xls：application/vnd.ms-excel，50.18 KB。数据集 DOI：10.1371/journal.pone.0087663。

【主题与分类】

源站学科分类：Biological Sciences、Medicine。主题标签：genetics、cytogenetics、Cytogenetic analysis、genomics、Comparative genomics、Molecular cell biology、Cellular types、cytometry、gene expression、oncology。

【适用方向】

源站学科分类标注为 Biological Sciences、Medicine。

【获取与许可】

源站页面：https://plos.figshare.com/articles/dataset/_Resolving_Tumor_Heterogeneity_Genes_Involved_in_Chordoma_Cell_Development_Identified_by_Low_Template_Analysis_of_Morphologically_Distinct_Cells_/925821

使用许可：CC BY 4.0（https://creativecommons.org/licenses/by/4.0/）。

规范引用：El-Heliebi, Amin; Kroneis, Thomas; Wagner, Karin; Meditz, Katharina; Kolb, Dagmar; Feichtinger, Julia; et al. (2016). Resolving Tumor Heterogeneity: Genes Involved in Chordoma Cell Development Identified by Low-Template Analysis of Morphologically Distinct Cells. PLOS ONE. Dataset

【使用注意】

· 源站最后修改于 2023-05-30，引用时请注意版本时效。