A novel estimator of between-study variance in random-effects models
Abstract Background With the rapid development of high-throughput sequencing technologies, many datasets on the same biological subject are generated. A meta-analysis is an approach that combines results from different studies on the same topic. The random-effects model in a meta-analysis enables th...
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doaj-03827e02dbe24acfb05c48fb82a0d9532021-02-14T12:22:23ZengBMCBMC Genomics1471-21642020-02-0121111610.1186/s12864-020-6500-9A novel estimator of between-study variance in random-effects modelsNan Wang0Jun Zhang1Li Xu2Jing Qi3Beibei Liu4Yiyang Tang5Yinan Jiang6Liang Cheng7Qinghua Jiang8Xunbo Yin9Shuilin Jin10School of Mathematics, Harbin Institute of TechnologyRehabilitation department, Heilongjiang Province Land Reclamation Headquarters General HospitalCollege of Computer Science and Technology, Harbin Engineering UniversitySchool of Mathematics, Harbin Institute of TechnologySchool of Mathematics, Harbin Institute of TechnologySchool of Mathematics, Heilongjiang UniversityHeilongjiang Province Hospital of Chinese MedicineCollege of Bioinformatics Science and Technology, Harbin Medical UniversitySchool of Life Science and Technology, Harbin Institute of TechnologySchool of Mathematics, Harbin Institute of TechnologySchool of Mathematics, Harbin Institute of TechnologyAbstract Background With the rapid development of high-throughput sequencing technologies, many datasets on the same biological subject are generated. A meta-analysis is an approach that combines results from different studies on the same topic. The random-effects model in a meta-analysis enables the modeling of differences between studies by incorporating the between-study variance. Results This paper proposes a moments estimator of the between-study variance that represents the across-study variation. A new random-effects method (DSLD2), which involves two-step estimation starting with the DSL estimate and the Dg2 $D_{g}^{2}$ in the second step, is presented. The DSLD2 method is compared with 6 other meta-analysis methods based on effect sizes across 8 aspects under three hypothesis settings. The results show that DSLD2 is a suitable method for identifying differentially expressed genes under the first hypothesis. The DSLD2 method is also applied to Alzheimer’s microarray datasets. The differentially expressed genes detected by the DSLD2 method are significantly enriched in neurological diseases. Conclusions The results from both simulationes and an application show that DSLD2 is a suitable method for detecting differentially expressed genes under the first hypothesis.https://doi.org/10.1186/s12864-020-6500-9Differentially expressed genesBetween-study varianceRandom-effects modelMeta-analysis |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Nan Wang Jun Zhang Li Xu Jing Qi Beibei Liu Yiyang Tang Yinan Jiang Liang Cheng Qinghua Jiang Xunbo Yin Shuilin Jin |
spellingShingle |
Nan Wang Jun Zhang Li Xu Jing Qi Beibei Liu Yiyang Tang Yinan Jiang Liang Cheng Qinghua Jiang Xunbo Yin Shuilin Jin A novel estimator of between-study variance in random-effects models BMC Genomics Differentially expressed genes Between-study variance Random-effects model Meta-analysis |
author_facet |
Nan Wang Jun Zhang Li Xu Jing Qi Beibei Liu Yiyang Tang Yinan Jiang Liang Cheng Qinghua Jiang Xunbo Yin Shuilin Jin |
author_sort |
Nan Wang |
title |
A novel estimator of between-study variance in random-effects models |
title_short |
A novel estimator of between-study variance in random-effects models |
title_full |
A novel estimator of between-study variance in random-effects models |
title_fullStr |
A novel estimator of between-study variance in random-effects models |
title_full_unstemmed |
A novel estimator of between-study variance in random-effects models |
title_sort |
novel estimator of between-study variance in random-effects models |
publisher |
BMC |
series |
BMC Genomics |
issn |
1471-2164 |
publishDate |
2020-02-01 |
description |
Abstract Background With the rapid development of high-throughput sequencing technologies, many datasets on the same biological subject are generated. A meta-analysis is an approach that combines results from different studies on the same topic. The random-effects model in a meta-analysis enables the modeling of differences between studies by incorporating the between-study variance. Results This paper proposes a moments estimator of the between-study variance that represents the across-study variation. A new random-effects method (DSLD2), which involves two-step estimation starting with the DSL estimate and the Dg2 $D_{g}^{2}$ in the second step, is presented. The DSLD2 method is compared with 6 other meta-analysis methods based on effect sizes across 8 aspects under three hypothesis settings. The results show that DSLD2 is a suitable method for identifying differentially expressed genes under the first hypothesis. The DSLD2 method is also applied to Alzheimer’s microarray datasets. The differentially expressed genes detected by the DSLD2 method are significantly enriched in neurological diseases. Conclusions The results from both simulationes and an application show that DSLD2 is a suitable method for detecting differentially expressed genes under the first hypothesis. |
topic |
Differentially expressed genes Between-study variance Random-effects model Meta-analysis |
url |
https://doi.org/10.1186/s12864-020-6500-9 |
work_keys_str_mv |
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