Computational and Structural Biotechnology Journal (Jan 2023)

IHGA: An interactive web server for large-scale and comprehensive discovery of genes of interest in hepatocellular carcinoma

  • Qiangnu Zhang,
  • Weibin Hu,
  • Lingfeng Xiong,
  • Jin Wen,
  • Teng Wei,
  • Lesen Yan,
  • Quan Liu,
  • Siqi Zhu,
  • Yu Bai,
  • Yuandi Zeng,
  • Zexin Yin,
  • Jilin Yang,
  • Wenjian Zhang,
  • Meilong Wu,
  • Yusen Zhang,
  • Gongze Peng,
  • Shiyun Bao,
  • Liping Liu

Journal volume & issue
Vol. 21
pp. 3987 – 3998

Abstract

Read online

Mining gene expression data is valuable for discovering novel biomarkers and therapeutic targets in hepatocellular carcinoma (HCC). Although emerging data mining tools are available for pan-cancer–related gene data analysis, few tools are dedicated to HCC. Moreover, tools specifically designed for HCC have restrictions such as small data scale and limited functionality. Therefore, we developed IHGA, a new interactive web server for discovering genes of interest in HCC on a large-scale and comprehensive basis. Integrative HCC Gene Analysis (IHGA) contains over 100 independent HCC patient-derived datasets (with over 10,000 tissue samples) and more than 90 cell models. IHGA allows users to conduct a series of large-scale and comprehensive analyses and data visualizations based on gene mRNA levels, including expression comparison, correlation analysis, clinical characteristics analysis, survival analysis, immune system interaction analysis, and drug sensitivity analysis. This method notably enhanced the richness of clinical data in IHGA. Additionally, IHGA integrates artificial intelligence (AI)–assisted gene screening based on natural language models. IHGA is free, user-friendly, and can effectively reduce time spent during data collection, organization, and analysis. In conclusion, IHGA is competitive in terms of data scale, data diversity, and functionality. It effectively alleviates the obstacles caused by HCC heterogeneity to data mining work and helps advance research on the molecular mechanisms of HCC.

Keywords