Severity: Warning
Message: file_get_contents(https://...@gmail.com&api_key=61f08fa0b96a73de8c900d749fcb997acc09&a=1): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests
Filename: helpers/my_audit_helper.php
Line Number: 197
Backtrace:
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 197
Function: file_get_contents
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 271
Function: simplexml_load_file_from_url
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 3165
Function: getPubMedXML
File: /var/www/html/application/controllers/Detail.php
Line: 597
Function: pubMedSearch_Global
File: /var/www/html/application/controllers/Detail.php
Line: 511
Function: pubMedGetRelatedKeyword
File: /var/www/html/index.php
Line: 317
Function: require_once
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Differential expression analysis is crucial in genomics, yet most methods focus only on mean shifts. Variance shifts in gene expression-especially in cellular signaling and aging-are increasingly recognized as being biologically important. We present QRscore (quantile rank score), a general non-parametric framework that extends the Mann-Whitney test to detect both mean and variance shifts through model-informed weights derived from negative binomial (NB) and zero-inflated NB (ZINB) distributions. QRscore offers high statistical power with false discovery rate (FDR) control, surpassing existing methods in detecting both types of distributional changes. When applied to bulk RNA sequencing (RNA-seq) data from Genotype-Tissue Expression (GTEx), QRscore uncovers numerous genes with dispersion shifts that are missed by mean-shift analysis. In pseudo-bulked single-cell RNA-seq data from the Asian Immune Diversity Atlas (AIDA), QRscore further reveals cell-type-specific variance shifts across age groups that remain undetectable in bulk analyses. QRscore augments the genome bioinformatics toolkit by offering a powerful and flexible approach for differential expression analysis.
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http://dx.doi.org/10.1016/j.crmeth.2025.101147 | DOI Listing |