Severity: Warning
Message: file_get_contents(https://...@pubfacts.com&api_key=b8daa3ad693db53b1410957c26c9a51b4908&a=1): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests
Filename: helpers/my_audit_helper.php
Line Number: 176
Backtrace:
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 176
Function: file_get_contents
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 250
Function: simplexml_load_file_from_url
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 1034
Function: getPubMedXML
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 3152
Function: GetPubMedArticleOutput_2016
File: /var/www/html/application/controllers/Detail.php
Line: 575
Function: pubMedSearch_Global
File: /var/www/html/application/controllers/Detail.php
Line: 489
Function: pubMedGetRelatedKeyword
File: /var/www/html/index.php
Line: 316
Function: require_once
A complex tissue contains a variety of cells with distinct molecular signatures. Single-cell RNA sequencing has characterized the transcriptomes of different cell types and enables researchers to discover the underlying mechanisms of cellular heterogeneity. A critical task in single-cell transcriptome studies is to uncover transcriptional differences among specific cell types. However, the intercellular transcriptional variation is usually confounded with high level of technical noise, which masks the important biological signals. Here, we propose a new computational method DiffGE for differential analysis, adopting network entropy to measure the expression dynamics of gene groups among different cell types and to identify the highly differential gene groups. To evaluate the effectiveness of our proposed method, DiffGE is applied to three independent single-cell RNA-seq datasets and to identify the highly dynamic gene groups that exhibit distinctive expression patterns in different cell types. We compare the results of our method with those of three widely applied algorithms. Further, the gene function analysis indicates that these detected differential gene groups are significantly related to cellular regulation processes. The results demonstrate the power of our method in evaluating the transcriptional dynamics and identifying highly differential gene groups among different cell types.
Download full-text PDF |
Source |
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7649823 | PMC |
http://dx.doi.org/10.3389/fcell.2020.588041 | DOI Listing |
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