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Kurylo, C.

Publications and source records attributed to Kurylo, C..

2 recordsLinked to original sources

HiCDOC: chromatin compartment prediction and differential analysis from Hi-C data with replicates

MotivationThe spatial organization of the genome plays an essential role in regulating cellular functions, with A/B chromatin compartments reflecting broad differences in transcriptional and epigenetic activity. Hi-C enables genome-wide identification of such compartments, but robust differential analysis between groups of samples remains challenging. Existing approaches largely rely on Principal Component Analysis, which, applied on Hi-C matrices separately, requires heuristic sign choices to merge results and does not naturally incorporate replicates. ResultsHere we present HiCDOC, a Bioconductor package for the prediction and differential analysis of chromatin compartments from Hi-C data with replicates. HiCDOC uses constrained k-means clustering to jointly analyze multiple Hi-C matrices, incorporating replicate information to enhance robustness, and provides empirical statistical support for predicted compartment switches. Applied to Hi-C datasets from human tissues and mouse cell lines, HiCDOC identified biologically relevant compartment changes supported by transcriptional differences. Comparisons with existing tools showed both overlap and complementarity, while a controlled benchmark with artificially introduced changes confirmed high sensitivity. Although extensively tested on pairwise comparisons, HiCDOC offers a flexible framework compatible with more complex designs and, in principle, with more than two compartment states. By combining replicate-aware clustering, automatic A/B assignment across chromosomes, extensive quality control, and statistical evaluation, HiCDOC provides an alternative and complementary approach to PCA-based methods for compartment analysis. HiCDOC thus expands the methodological toolkit for exploring 3D genome dynamics and its role in cellular processes. AvailabilityHiCDOC is implemented in R and C++, and is available on Bioconductor: https://bioconductor.org/packages/release/bioc/html/HiCDOC.html Contactsylvain.foissac@inrae.fr

bioinformatics↗

Empowering bioinformatics communities with Nextflow and nf-core

Standardised analysis pipelines are an important part of FAIR bioinformatics research. Over the last decade, there has been a notable shift from point-and-click pipeline solutions such as Galaxy towards command-line solutions such as Nextflow and Snakemake. We report on recent developments in the nf-core and Nextflow frameworks that have led to widespread adoption across many scientific communities. We describe how adopting nf-core standards enables faster development, improved interoperability, and collaboration with the >8,000 members of the nf-core community. The recent development of Nextflow Domain-Specific Language 2 (DSL2) allows pipeline components to be shared and combined across projects. The nf-core community has harnessed this with a library of modules and subworkflows that can be integrated into any Nextflow pipeline, enabling research communities to progressively transition to nf-core best practices. We present a case study of nf-core adoption by six European research consortia, grouped under the EuroFAANG umbrella and dedicated to farmed animal genomics. We believe that the process outlined in this report can inspire many large consortia to seek harmonisation of their data analysis procedures.

bioinformatics↗