Author

Daniel Muliaditan

Agency for Science, Technology and ResearchORCID 0000-0001-7277-9744Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Cancer Biology· 2 Genomics· 1

Signature Assays, Organisms & Methods

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Organism:human· 3 Research Focus:differential expression· 2 Approach:experimental assay· 2 Research Focus:gene regulatory network inference· 2 Research Focus:variant calling· 2 Assay:whole-genome sequencing· 2 Assay:ChIP-seq· 1 Research Focus:chromatin & epigenetic regulation· 1

Frequent Co-Authors

Ramanuj DasGuptaiD· 2 shared Aditi GnanasekariD· 1 shared Andy Wing Chun PangiD· 1 shared Ann H. CapliniD· 1 shared Biswanath ChowdhuryiD· 1 shared Ceyda ÇoruhiD· 1 shared Chiea Chuen KhoriD· 1 shared Christelle En Lin ChuaiD· 1 shared

Activity by Year

2024-2025 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 24 mutual co-author links

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2 shared papersCancer Biology

Ramanuj DasGuptaORCID

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3 papers

Recent·Most cited

GenomicsbioRxivPreprintJul 12, 2025

A Complete Telomere-to-Telomere Diploid Reference Genome for Indian Population

Prasad Sarashetti, Josipa Lipovac, Jia Qi…·Jianjun Liu

The paper presents a high-quality, gapless diploid reference genome for an Indian population, revealing extensive structural variation and improved performance for genomic analysis in South Asian samples.

8 citations

humanwhole-genome sequencing

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Cancer BiologyNature CommunicationsPeer-reviewedFeb 10, 2025

Breakage fusion bridge cycles drive high oncogene copy number, but not intratumoral genetic heterogeneity or rapid cancer genome change

Siavash R. Dehkordi, Ivy Tsz-Lo Wong, Jing Ni…·Vineet Bafna

The paper introduces OM2BFB, an algorithm detecting BFB amplifications using OGMs, showing high precision and recall, and finds BFB events are common in certain cancers but not linked to intratumoral heterogeneity or rapid genome change.

30 citationstop 1%

humanwhole-genome sequencing

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Cancer BiologybioRxivPreprintFeb 14, 2024

Deciphering the function of intrinsic and genomics-driven epigenetic heterogeneity in head and neck cancer progression with single-nucleus CUT&RUN

Howard John Womersley, Daniel Muliaditan, Ramanuj DasGupta, Lih Feng Cheow

This study develops a single-nucleus CUT&RUN assay to analyze histone modifications in HNSCC cell lines, revealing how epigenetic changes contribute to cancer progression and heterogeneity.

DOI 10.1101/2024.02.14.580230

humanChIP-seq

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