Suppr超能文献

使用细胞条形码技术对细胞进行克隆分析:数量和大小的重要性

Clonal Analysis of Cells with Cellular Barcoding: When Numbers and Sizes Matter.

作者信息

Bystrykh Leonid V, Belderbos Mirjam E

机构信息

Laboratory of Ageing Biology and Stem Cells, European Research Institute for the Biology of Ageing, University Medical Center Groningen, University of Groningen, Antonius Deusinglaan 1, Building 3226, Groningen, 9713, AV, The Netherlands.

Department of Pediatrics, University Medical Center Groningen, Groningen, The Netherlands.

出版信息

Methods Mol Biol. 2016;1516:57-89. doi: 10.1007/7651_2016_343.

Abstract

Cellular barcoding is a recently rediscovered tool to trace the clonal output of individual cells with genetically distinct and heritable DNA sequences. Each year a few dozens of papers are published using the cellular barcoding technique. Those publications largely focus on mutually related issues, namely: counting cells capable of clonal proliferation and expansion, monitoring clonal dynamics in time, tracing the origin of differentiated cells, characterizing the differentiation potential of stem cells and similar topics. Apart from their biological content, claims and conclusions, these studies show remarkable diversity in technical aspects of the barcoding method and sometimes in major conclusions. Although a diversity of approaches is quite usual in data analysis, deviant handling of barcode data might directly affect experimental results and their biological interpretation. Here, we will describe typical challenges and caveats in cellular barcoding publications available so far.

摘要

细胞条形码技术是一种最近重新发现的工具,用于追踪具有遗传上不同且可遗传的DNA序列的单个细胞的克隆输出。每年都有几十篇使用细胞条形码技术的论文发表。这些出版物主要集中在相互关联的问题上,即:对能够进行克隆增殖和扩增的细胞进行计数,及时监测克隆动态,追踪分化细胞的起源,表征干细胞的分化潜能以及类似主题。除了它们的生物学内容、主张和结论外,这些研究在条形码方法的技术方面有时甚至在主要结论上都表现出显著的多样性。尽管在数据分析中采用多种方法是很常见的,但对条形码数据的异常处理可能会直接影响实验结果及其生物学解释。在这里,我们将描述迄今为止细胞条形码出版物中的典型挑战和注意事项。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验