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Related Concept Videos

Genomics02:02

Genomics

Genomics is the science of genomes: it is the study of all the genetic material of an organism. In humans, the genome consists of information carried in 23 pairs of chromosomes in the nucleus, as well as mitochondrial DNA. In genomics, both coding and non-coding DNA is sequenced and analyzed. Genomics allows a better understanding of all living things, their evolution, and their diversity. It has a myriad of uses: for example, to build phylogenetic trees, to improve productivity and...
Genome Annotation and Assembly03:36

Genome Annotation and Assembly

The genome refers to all of the genetic material in an organism. It can range from a few million base pairs in microbial cells to several billion base pairs in many eukaryotic organisms. Genome assembly refers to the process of taking the DNA sequencing data and putting it all back together in a correct order to create a close representation of the original genome. This is followed by the identification of functional elements on the newly assembled genome, a process called genome annotation.
Proteomics01:33

Proteomics

A proteome is the entire set of proteins that a cell type produces. We can study proteomes using the knowledge of genomes because genes code for mRNAs, and the mRNAs encode proteins. Although mRNA analysis is a step in the right direction, not all mRNAs are translated into proteins.
Proteomics is the study of proteomes' function. It involves the large-scale systematic study of the proteome to denote the protein complement expressed by a genome. Scientist Mark Wilkins coined the term proteomics...

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Related Experiment Video

Updated: Jun 18, 2026

DeepOmicsAE: Representing Signaling Modules in Alzheimer's Disease with Deep Learning Analysis of Proteomics, Metabolomics, and Clinical Data
09:47

DeepOmicsAE: Representing Signaling Modules in Alzheimer's Disease with Deep Learning Analysis of Proteomics, Metabolomics, and Clinical Data

Published on: December 15, 2023

IAN, an intelligent system for omics data analysis and discovery.

Vijayaraj Nagarajan1, Reiko Horai1, Guangpu Shi1

  • 1Laboratory of Immunology, National Eye Institute, NIH, Bethesda, MD 20892, USA.

Cell Reports Methods
|June 16, 2026
PubMed
Summary

IAN, an AI-driven R package, integrates and interprets gene expression data using large language models. It provides biological insights by analyzing pathway and regulatory information for researchers.

Keywords:
CP: computational biologyCP: systems biologyLLM groundingLLMsbiological discoverygene regulationlarge language modelsmulti-agent AInetwork analysisomics data analysispathway enrichmentreproducibility

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Last Updated: Jun 18, 2026

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IR-TEx: An Open Source Data Integration Tool for Big Data Transcriptomics Designed for the Malaria Vector Anopheles gambiae
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IR-TEx: An Open Source Data Integration Tool for Big Data Transcriptomics Designed for the Malaria Vector Anopheles gambiae

Published on: January 15, 2020

Area of Science:

  • Bioinformatics
  • Computational Biology
  • Artificial Intelligence in Genomics

Background:

  • Gene expression data analysis is complex.
  • Integrating diverse biological datasets (pathways, regulatory networks, protein-protein interactions) is challenging.
  • Interpreting large-scale transcriptomic data requires advanced computational tools.

Purpose of the Study:

  • To introduce IAN, an R package for artificial intelligence-driven gene expression data integration and interpretation.
  • To leverage large language models (LLMs) for summarizing and explaining enrichment analysis results.
  • To provide researchers with data-driven insights, system overviews, and key regulator identification.

Main Methods:

  • Utilizes popular pathway databases (KEGG, WikiPathways, Reactome, GO) and regulatory datasets (ChEA).
  • Integrates protein-protein interaction data from STRING.
  • Employs a multi-agent architecture with LLMs for summarizing and interpreting enrichment analysis results.
  • Applies engineered prompts and grounding instructions to guide LLM interpretation.

Main Results:

  • Demonstrates IAN's functionality on published human transcriptomic data.
  • Evaluates the robustness of IAN's performance across different LLMs.
  • Presents human expert evaluations confirming the clarity and relevance of IAN's outputs.
  • Provides explanations, system overviews, key regulators, and data-driven insights.

Conclusions:

  • IAN offers a novel approach to gene expression data analysis by integrating AI and LLMs.
  • The package facilitates the interpretation of complex transcriptomic data, enhancing biological discovery.
  • IAN's modular design and expert-validated outputs make it a valuable tool for researchers.