Sajib Acharjee Dip

dblp:372/5329 · DBLP profile ↗
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2ranked-venue papers
1as first author
2since 2021 · last 2026
0009-0007-0959-2638ORCID · verified

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

Artificial intelligence and machine learning · 1 · 1 first-author · 1 since 2021Applied, interdisciplinary, general and emerging computing · 1 · 1 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 1 heaviest of 1, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology
single-cell biology
1.012026
LLM4Cell: Taxonomy and Evaluation of LLM and Agentic Models for Single-Cell Biology · ACL (1) 2026

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

large language model · 1.0agentic model · 1.0
YearPublicationVenuePosition
2026 LLM4Cell: Taxonomy and Evaluation of LLM and Agentic Models for Single-Cell Biology
abstract
Sajib Acharjee Dip, Adrika Zafor, Bikash Kumar Paul, Uddip Acharjee Shuvo, Muhit Islam Emon, Xuan Wang, Liqing Zhang. Proceedings of the 64th Annual Meeting of the Association for Computational Linguistics (Volume 1: Long Papers). 2026.
Sajib Acharjee Dip, Adrika Zafor, Bikash Kumar Paul, Uddip Acharjee Shuvo, Muhit Islam Emon, Xuan Wang 0008, Liqing Zhang 0002
ACL (1)1
2025 UnCOT-AD: Unpaired Cross-Omics Translation Enables Multi-Omics Integration for Alzheimer's Disease Prediction
abstract
Alzheimer's Disease (AD) is a progressive neurodegenerative disorder, posing a growing public health challenge. Traditional machine learning models for AD prediction have relied on single omics data or phenotypic assessments, limiting their ability to capture the disease's molecular complexity and resulting in poor performance. Recent advances in high-throughput multi-omics have provided deeper biological insights. However, due to the scarcity of paired omics datasets, existing multi-omics AD prediction models rely on unpaired omics data, where different omics profiles are combined without being derived from the same biological sample, leading to biologically less meaningful pairings and causing less accurate predictions. To address these issues, we propose UnCOT-AD, a novel deep learning framework for Unpaired Cross-Omics Translation enabling effective multi-omics integration for AD prediction. Our method introduces the first-ever cross-omics translation model trained on unpaired omics datasets, using two coupled Variational Autoencoders and a novel cycle consistency mechanism to ensure accurate bidirectional translation between omics types. We integrate adversarial training to ensure that the generated omics profiles are biologically realistic. Moreover, we employ contrastive learning to capture the disease specific patterns in latent space to make the cross-omics translation more accurate and biologically relevant. We rigorously validate UnCOT-AD on both cross-omics translation and AD prediction tasks. Results show that UnCOT-AD empowers multi-omics based AD prediction by combining real omics profiles with corresponding omics profiles generated by our cross-omics translation module and achieves state-of-the-art performance in accuracy and robustness. Source code is available at https://github.com/abrarrahmanabir/UnCOT-AD.
Abrar Rahman Abir, Sajib Acharjee Dip, Liqing Zhang 0002
Briefings Bioinform.2