SynthesisBMC genomics2025
DSLE2 random-effects meta-analysis model for high-throughput methylation data.
Synthesis in BMC genomics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Authors and funding
4 authors.
Funding
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Abstract
backgroundWith the rapid development of high-throughput sequencing technology, high-throughput sequencing data has grown on a massive scale, leading to the emergence of multiple public databases, such as EBI and GEO. Conducting secondary mining of high-throughput sequencing data in these databases can yield more valuable insights. Meta-analysis can quantitatively combine high-throughput sequencing data from the the same topic. It increases the sample size for data analysis, enhances statistical power, and results in more consistent and reliable conclusions.
resultsThis study proposes a new between-study variance estimator
conclusionsThis paper propose the DSLE2 random-effects meta-analysis model based on new between-study variance estimator Em. The DSLE2 model performs well for methylation data.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.