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转录组多样性是 RNA 测序数据中系统性变异的一个来源。

Transcriptome diversity is a systematic source of variation in RNA-sequencing data.

机构信息

Department of Biology, Stanford University, Stanford, California, United States of America.

出版信息

PLoS Comput Biol. 2022 Mar 24;18(3):e1009939. doi: 10.1371/journal.pcbi.1009939. eCollection 2022 Mar.

Abstract

RNA sequencing has been widely used as an essential tool to probe gene expression. While standard practices have been established to analyze RNA-seq data, it is still challenging to interpret and remove artifactual signals. Several biological and technical factors such as sex, age, batches, and sequencing technology have been found to bias these estimates. Probabilistic estimation of expression residuals (PEER), which infers broad variance components in gene expression measurements, has been used to account for some systematic effects, but it has remained challenging to interpret these PEER factors. Here we show that transcriptome diversity-a simple metric based on Shannon entropy-explains a large portion of variability in gene expression and is the strongest known factor encoded in PEER factors. We then show that transcriptome diversity has significant associations with multiple technical and biological variables across diverse organisms and datasets. In sum, transcriptome diversity provides a simple explanation for a major source of variation in both gene expression estimates and PEER covariates.

摘要

RNA 测序已被广泛用作探测基因表达的重要工具。虽然已经建立了标准的方法来分析 RNA-seq 数据,但解释和去除人为信号仍然具有挑战性。已经发现了几个生物学和技术因素,如性别、年龄、批次和测序技术,这些因素会影响这些估计。概率表达残差估计(PEER)用于推断基因表达测量中的广泛方差分量,以解释一些系统效应,但解释这些 PEER 因素仍然具有挑战性。在这里,我们表明转录组多样性——基于香农熵的简单度量——解释了基因表达变异性的很大一部分,并且是 PEER 因子中编码的最强已知因素。然后,我们表明转录组多样性与不同生物体和数据集的多个技术和生物学变量具有显著关联。总之,转录组多样性为基因表达估计和 PEER 协变量的主要变异源提供了一个简单的解释。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2169/8982896/31894f85b7e7/pcbi.1009939.g001.jpg

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