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Giorgia Migliaccio

dblp:421/2410 · DBLP profile ↗
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2ranked-venue papers
1as first author
2since 2021 · last 2026
0000-0003-0552-0155ORCID · corroborated

Domains — the database's venue-derived domains; a paper can count in several

Applied, interdisciplinary, general and emerging computing · 2 · 1 first-author · 2 since 2021

Expertise — from the expertise taxonomy: the topics of the expert's papers under the CCF categories. A weight counts papers with recency: 1 for a paper about the topic, 0.3 when the topic is its context, halved every five years.

Interdisciplinary, comprehensive, and emerging computing
1 paper
Bioinformatics and computational biology · 100%

Topics — the 2 heaviest of 2, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › epigenomics › DNA methylation
DNA methylation analysis
0.912025
OpTiles: an R package for adaptive tiling and methylation variability profiling · Bioinform. 2025
Bioinformatics and computational biology
epigenomics
0.912025
OpTiles: an R package for adaptive tiling and methylation variability profiling · Bioinform. 2025

Methods — techniques the papers use, named apart from their topics

reliability metric computation · 0.9dynamic tiling window definition · 0.9
YearPublicationVenuePosition
2026 MUUMI: an R package for statistical and network-based meta-analysis for multi-omics data integration
abstract
BACKGROUND: Disentangling physiopathological mechanisms of biological systems through high-level integration of omics data has become a standard procedure in life sciences. However, platform heterogeneity, batch effects, and the lack of unified methods for single- and multi-omics analyses represent relevant drawbacks that hinder the extrapolation of a meaningful biological interpretation. While statistical meta-analysis is widely used to integrate several omics datasets of the same type, it does not allow the integration of multi-modal data deriving from multi-omics experiments. Network science is at the forefront of systems biology, where the inference of molecular interactomes allowed the investigation of perturbed biological systems, by shedding light on the disrupted relationships that keep the homeostasis of complex systems. RESULTS: Here, we present MUUMI, an R package that unifies statistical meta-analysis and network-based omics data integration within a single analytical framework. MUUMI allows the identification of robust molecular signatures through multiple meta-analytical methods, inference and analysis of molecular interactomes and the integration of multiple omics layers through similarity network fusion. We demonstrate the functionalities of MUUMI by presenting two case studies in which we analysed (1) 17 transcriptomic datasets on idiopathic pulmonary fibrosis (IPF) from both microarray and RNA-Seq platforms and (2) multi-omics data of THP-1 macrophages exposed to different polarising stimuli. In both examples, MUUMI revealed biologically coherent signatures, underscoring its value in elucidating complex biological processes. CONCLUSIONS: MUUMI leverages omics data meta-analysis, integration and interpretation that implements both traditional and network-based approaches to unleash the power of multi-study datasets. Statistical and network-based approaches are integrated in a unique framework, allowing the user to derive robust and biologically meaningful results from different studies and datasets. MUUMI is an open-source package and is freely available at https://github.com/fhaive/muumi .
Simo Iisakki Inkala, Michele Fratello, Giusy del Giudice, Giorgia Migliaccio, Angela Serra, Dario Greco, Antonio Federico
BMC Bioinform.4
2025 OpTiles: an R package for adaptive tiling and methylation variability profiling
abstract
SUMMARY: OpTiles is an R package that dynamically defines tiling windows based on the distribution of sequenced CpGs, addressing the limitations of traditional fixed-tiling approaches in targeted methylation datasets. By integrating CpG density with intra-region methylation variability, it provides a reliability metric and extended functionality for annotating, prioritizing, and interpreting complex methylation data. AVAILABILITY AND IMPLEMENTATION: OpTiles is implemented in R and source code is freely available at https://github.com/fhaive/OpTiles. Data are available on Zenodo at https://doi.org/10.5281/zenodo.16961292.
Giorgia Migliaccio, Lena Möbus, Giusy del Giudice, Jack Morikka, Antonio Federico, Angela Serra, Dario Greco
Bioinform.1