পদ্ধতির তুলনা করুন

	নেটওয়ার্ক-ভিত্তিক এপিজিনোম-ওয়াইড অ্যাসোসিয়েশন স্টাডি (Network EWAS)	নেটওয়ার্ক-ভিত্তিক GWAS
ক্ষেত্র	জৈব তথ্যবিজ্ঞান	জৈব তথ্যবিজ্ঞান
পরিবার	Process / pipeline	Process / pipeline
উদ্ভবের বছর	2010s, consolidating 2012–2018	2011–2013 (early tools); mature framework by 2015
প্রবর্তক	Adapted from EWAS (Rakyan et al., 2011) and network-based genomic methods (e.g., Ideker & Sharan, 2008)	Jia et al. (dmGWAS, 2011); Baranzini et al.; multiple concurrent groups
ধরন	Integrative epigenomic analysis	Network-augmented association analysis
মৌলিক উৎস	Rakyan, V. K., Down, T. A., Balding, D. J., & Beck, S. (2011). Epigenome-wide association studies for common human diseases. Nature Reviews Genetics, 12(8), 529–541.	Wang, Q., Yu, H., Zhao, Z., & Jia, P. (2015). EW_dmGWAS: edge-weighted dense module search for genome-wide association studies and gene expression profiles. Bioinformatics, 31(15), 2591–2594.
অপর নাম	network EWAS, network-integrated EWAS, graph-based EWAS, network-based DNA methylation analysis	network GWAS, gene network GWAS, network-informed GWAS, NbGWAS
সম্পর্কিত	6	6
সারসংক্ষেপ	Network-based EWAS extends conventional epigenome-wide association studies by overlaying differentially methylated positions or regions onto biological interaction networks — such as protein-protein interaction, co-expression, or gene regulatory networks — to identify functionally coherent epigenetic modules rather than isolated CpG hits. This integration increases statistical power for detecting weak signals and reveals coordinated epigenetic dysregulation across pathways.	Network-based GWAS integrates conventional genome-wide association study results with biological network data — such as protein-protein interaction (PPI) networks or gene co-expression graphs — to identify disease-relevant gene modules or subnetworks. Instead of reporting only the top individual SNPs, this approach propagates association signals through molecular interaction networks, surfacing gene clusters whose collective signal implicates them in complex-trait biology even when no single variant reaches genome-wide significance alone.