LineageProfiler:哺乳动物转录组细胞类型识别的自动分类和可视化

N. Salomonis
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摘要

微阵列和下一代RNA测序方法都极大地提高了我们检测生物体发育和疾病背后的转录物变异的能力。虽然存在许多工具来评估基因和转录物变异,但相对于数百种已知的成人和祖细胞类型,评估细胞类型身份的方法缺乏。这种方法是迫切需要的,以了解哪些细胞类型存在于一个生物样本中,特别是在谱系限制体外干细胞分化。我们已经开发了LineageProfiler作为AltAnalyze分析包(http://www.altanalyze.org)的一个组成部分,用于分析和可视化转录组与组织,分离细胞类型或祖细胞状态的大概要的相关性。与相关方法不同,LineageProfiler可以利用来自微阵列或下一代测序数据的基因或外显子表达谱来推导相关性。相关的Z分数自动可视化沿着一个全面的谱系网络或作为一个聚集的热图。通过与GO-Elite (http://www.genmapp.org/go_elite)工具的整合,潜在的生物标志物用于评估条件和样品之间细胞类型的富集。这种方法已经成功地从RNA-Seq中准确地鉴定出体外分化细胞的已知群体,从混合组织实验中测量细胞类型的相对丰度,并鉴定由于不一致的组织解剖而造成的污染。
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LineageProfiler: Automated Classification and Visualization of Cell Type Identity for Mammalian Transcriptomes
Both microarray and next generation RNA sequencing methods have vastly improved our ability to detect transcript variation underlying organism development and disease. While many tools exist to assess gene and transcript variation, there is a paucity of methods to evaluate cell type identity relative to the hundreds of known adult and progenitor cell types. Such methods are sorely needed to understand which cell types are present within a biological sample, particularly during lineage restricted in vitro stem cell differentiation. We have developed LineageProfiler as a component of the AltAnalyze analysis package (http://www.altanalyze.org), to analyze and visualize transcriptome correlations to a large compendium of tissues, isolated cell types or progenitor states. Unlike related methods, LineageProfiler can utilize gene or exon expression profiles from either microarray or next generation sequencing data to derive correlations. Associated Z scores are automatically visualized along a comprehensive lineage network or as a clustered heatmap. Through integration with the tool GO-Elite (http://www.genmapp.org/go_elite), underlying biomarkers are used to evaluate enrichment of cell types between conditions and samples. This approach has been successful at accurately identifying known populations of differentiating cells in vitro from RNA-Seq, measuring the relative abundance of cell types from mixed tissue experiments and identifying contamination due to inconsistent tissue dissection.
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