scholarly journals Statistical Analysis of Spatial Expression Pattern for Spatially Resolved Transcriptomic Studies

2019 ◽  
Author(s):  
Shiquan Sun ◽  
Jiaqiang Zhu ◽  
Xiang Zhou

ABSTRACTRecent development of various spatially resolved transcriptomic techniques has enabled gene expression profiling on complex tissues with spatial localization information. Identifying genes that display spatial expression pattern in these studies is an important first step towards characterizing the spatial transcriptomic landscape. Detecting spatially expressed genes requires the development of statistical methods that can properly model spatial count data, provide effective type I error control, have sufficient statistical power, and are computationally efficient. Here, we developed such a method, SPARK. SPARK directly models count data generated from various spatial resolved transcriptomic techniques through generalized linear spatial models. With a new efficient penalized quasi-likelihood based algorithm, SPARK is scalable to data sets with tens of thousands of genes measured on tens of thousands of samples. Importantly, SPARK relies on newly developed statistical formulas for hypothesis testing, producing well-calibrated p-values and yielding high statistical power. We illustrate the benefits of SPARK through extensive simulations and in-depth analysis of four published spatially resolved transcriptomic data sets. In the real data applications, SPARK is up to ten times more powerful than existing approaches. The high power of SPARK allows us to identify new genes and pathways that reveal new biology in the data that otherwise cannot be revealed by existing approaches.

2018 ◽  
Vol 20 (6) ◽  
pp. 2055-2065 ◽  
Author(s):  
Johannes Brägelmann ◽  
Justo Lorenzo Bermejo

Abstract Technological advances and reduced costs of high-density methylation arrays have led to an increasing number of association studies on the possible relationship between human disease and epigenetic variability. DNA samples from peripheral blood or other tissue types are analyzed in epigenome-wide association studies (EWAS) to detect methylation differences related to a particular phenotype. Since information on the cell-type composition of the sample is generally not available and methylation profiles are cell-type specific, statistical methods have been developed for adjustment of cell-type heterogeneity in EWAS. In this study we systematically compared five popular adjustment methods: the factored spectrally transformed linear mixed model (FaST-LMM-EWASher), the sparse principal component analysis algorithm ReFACTor, surrogate variable analysis (SVA), independent SVA (ISVA) and an optimized version of SVA (SmartSVA). We used real data and applied a multilayered simulation framework to assess the type I error rate, the statistical power and the quality of estimated methylation differences according to major study characteristics. While all five adjustment methods improved false-positive rates compared with unadjusted analyses, FaST-LMM-EWASher resulted in the lowest type I error rate at the expense of low statistical power. SVA efficiently corrected for cell-type heterogeneity in EWAS up to 200 cases and 200 controls, but did not control type I error rates in larger studies. Results based on real data sets confirmed simulation findings with the strongest control of type I error rates by FaST-LMM-EWASher and SmartSVA. Overall, ReFACTor, ISVA and SmartSVA showed the best comparable statistical power, quality of estimated methylation differences and runtime.


2006 ◽  
Vol 28 (63) ◽  
Author(s):  
Jane E. Gabriel ◽  
Vasco A. C. Azevedo ◽  
Philippe Langella

In the present report, we describe how Lactococcus lactis strains ectopically express the internalin-A protein from Listeria monocytogenes at the cell surface, situated specifically under the bacterial septum region. Such findings provide relevant insights into the spatial expression pattern of exogenous genes in lactic bacteria.


1993 ◽  
Vol 23 (4) ◽  
pp. 871-879 ◽  
Author(s):  
N. J. Goddard ◽  
M. A. Dunn ◽  
L. Zhang ◽  
A. J. White ◽  
P. L. Jack ◽  
...  

2002 ◽  
Vol 43 (3) ◽  
pp. 307-313 ◽  
Author(s):  
Kazumaru Miyoshi ◽  
Yasuaki Kagaya ◽  
Yuichirou Ogawa ◽  
Yasuo Nagato ◽  
Tsukaho Hattori

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