Integrative In Silico Analysis of Genome-Wide DNA Methylation Profiles in Schizophrenia

2020 ◽  
Vol 70 (11) ◽  
pp. 1887-1893
Author(s):  
Diego A. Forero ◽  
Yeimy González-Giraldo
2012 ◽  
Vol 13 (4) ◽  
pp. 5112-5124 ◽  
Author(s):  
Chang-Cai Liu ◽  
Bao-Guang Liu ◽  
Zhi-Wei Yang ◽  
Chun-Ming Li ◽  
Bai-Chen Wang ◽  
...  

2021 ◽  
Vol 21 (1) ◽  
Author(s):  
Haoyi Wang ◽  
Qian Wang ◽  
Haksong Pak ◽  
Tao Yan ◽  
Mingxun Chen ◽  
...  

Abstract Background Rapeseed (Brassica napus L.) is an important oil crop world-widely cultivated, and seed oil content (SOC) is one of the most important traits for rapeseed. To increase SOC, many efforts for promoting the function of genes on lipid biosynthesis pathway have been previously made. However, seed oil formation is a dynamic balance between lipid synthesis and breakdown. It is, therefore, also reasonable to weaken or eliminate the function of genes involved in lipid degradation for a higher final SOC. Results We applied a genome-wide association study (GWAS) on SOC in a collection of 290 core germplasm accessions. A total of 2,705,480 high-quality SNPs were used in the GWAS, and we identified BnaC07g30920D, a patatin-like lipase (PTL) gene, that was associated with SOC. In particular, six single-nucleotide-polymorphisms (SNPs) in the promoter region of BnaC07g30920D were associated with the significant reduction of SOC, leading to a 4.7–6.2% reduction of SOCs. We performed in silico analysis to show a total of 40 PTLs, which were divided into four clades, evenly distributed on the A and C subgenomes of Brassica napus. RNA-seq analysis unveiled that BnPTLs were preferentially expressed in reproductive tissues especially maturing seeds. Conclusions We identified BnaC07g30920D, a BnPTL gene, that was associated with SOC using GWAS and performed in silico analysis of 40 PTLs in Brassica napus. The results enrich our knowledge about the SOC formation in rapeseed and facilitate the future study in functional characterization of BnPTL genes.


Cells ◽  
2020 ◽  
Vol 9 (1) ◽  
pp. 165
Author(s):  
L. Francisco Lorenzo-Martín ◽  
Xosé R. Bustelo

The stem cells located in the hair follicle bulge area are critical for skin regeneration and repair. To date, little is known about the evolution of the transcriptome of these cells across time. Here, we have combined genome-wide expression analyses and a variety of in silico tools to determine the age-dependent evolution of the transcriptome of those cells. Our results reveal that the transcriptome of skin stem cells fluctuates extensively along the lifespan of mice. The use of both unbiased and pathway-centered in silico approaches has also enabled the identification of biological programs specifically regulated at those specific time-points. It has also unveiled hubs of highly transcriptionally interconnected genes and transcriptional factors potentially located at the core of those age-specific changes.


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