数据集包括全血基因表达谱和匹配的白细胞计数,可用于对细胞解卷积管道进行基准测试。

IF 1.9 Q3 GENETICS & HEREDITY BMC genomic data Pub Date : 2024-05-07 DOI:10.1186/s12863-024-01223-z
Grant C O'Connell
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引用次数: 0

摘要

目的:细胞解卷积是一种有价值的计算过程,它可以从大量 RNA 序列数据中推断出异质组织样本的细胞组成。基准测试是开发和评估新的细胞解卷积算法的关键步骤,在为特定实验应用建立和优化解卷积管道的过程中也发挥着关键作用。然而,活体基准数据集很少,尤其是全血数据集,而全血是剖析最多的人体组织。在这里,我们描述了一个独特的数据集,该数据集包含来自大量人体捐献者的全血基因表达谱和匹配的循环白细胞计数,可用于细胞解卷积管道的基准测试:为了生成该数据集,我们从一家学术医疗中心招募的 138 名捐献者身上采集了静脉全血样本。随后通过下一代 RNA 测序进行了全基因组表达谱分析,并使用流式细胞仪同时收集了白细胞差异。最终的数据集包含超过 45,000 个蛋白编码基因和非蛋白编码基因的供体级表达数据,以及匹配的中性粒细胞、淋巴细胞、单核细胞和嗜酸性粒细胞计数。
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Dataset including whole blood gene expression profiles and matched leukocyte counts with utility for benchmarking cellular deconvolution pipelines.

Objectives: Cellular deconvolution is a valuable computational process that can infer the cellular composition of heterogeneous tissue samples from bulk RNA-sequencing data. Benchmark testing is a crucial step in the development and evaluation of new cellular deconvolution algorithms, and also plays a key role in the process of building and optimizing deconvolution pipelines for specific experimental applications. However, few in vivo benchmarking datasets exist, particularly for whole blood, which is the single most profiled human tissue. Here, we describe a unique dataset containing whole blood gene expression profiles and matched circulating leukocyte counts from a large cohort of human donors with utility for benchmarking cellular deconvolution pipelines.

Data description: To produce this dataset, venous whole blood was sampled from 138 total donors recruited at an academic medical center. Genome-wide expression profiling was subsequently performed via next-generation RNA sequencing, and white blood cell differentials were collected in parallel using flow cytometry. The resultant final dataset contains donor-level expression data for over 45,000 protein coding and non-protein coding genes, as well as matched neutrophil, lymphocyte, monocyte, and eosinophil counts.

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