Selected article for: "cancer type and RNA seq"

Author: Carrillo-Perez, Francisco; Morales, Juan Carlos; Castillo-Secilla, Daniel; Molina-Castro, Yésica; Guillén, Alberto; Rojas, Ignacio; Herrera, Luis Javier
Title: Non-small-cell lung cancer classification via RNA-Seq and histology imaging probability fusion
  • Cord-id: dgf96gx1
  • Document date: 2021_9_22
  • ID: dgf96gx1
    Snippet: BACKGROUND: Adenocarcinoma and squamous cell carcinoma are the two most prevalent lung cancer types, and their distinction requires different screenings, such as the visual inspection of histology slides by an expert pathologist, the analysis of gene expression or computer tomography scans, among others. In recent years, there has been an increasing gathering of biological data for decision support systems in the diagnosis (e.g. histology imaging, next-generation sequencing technologies data, cl
    Document: BACKGROUND: Adenocarcinoma and squamous cell carcinoma are the two most prevalent lung cancer types, and their distinction requires different screenings, such as the visual inspection of histology slides by an expert pathologist, the analysis of gene expression or computer tomography scans, among others. In recent years, there has been an increasing gathering of biological data for decision support systems in the diagnosis (e.g. histology imaging, next-generation sequencing technologies data, clinical information, etc.). Using all these sources to design integrative classification approaches may improve the final diagnosis of a patient, in the same way that doctors can use multiple types of screenings to reach a final decision on the diagnosis. In this work, we present a late fusion classification model using histology and RNA-Seq data for adenocarcinoma, squamous-cell carcinoma and healthy lung tissue. RESULTS: The classification model improves results over using each source of information separately, being able to reduce the diagnosis error rate up to a 64% over the isolate histology classifier and a 24% over the isolate gene expression classifier, reaching a mean F1-Score of 95.19% and a mean AUC of 0.991. CONCLUSIONS: These findings suggest that a classification model using a late fusion methodology can considerably help clinicians in the diagnosis between the aforementioned lung cancer cancer subtypes over using each source of information separately. This approach can also be applied to any cancer type or disease with heterogeneous sources of information. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12859-021-04376-1.

    Search related documents:
    Co phrase search for related documents
    • adjacent tissue and lung tissue: 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11
    • adjacent tissue and lymph node: 1, 2, 3, 4
    • adjacent tissue and lymph node metastasis: 1, 2, 3
    • luad patient and lung cancer: 1
    • luad tissue and lung tissue: 1
    • luad tissue lusc and lung tissue: 1
    • lung cancer and lymph node: 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25
    • lung cancer and lymph node metastasis: 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14
    • lung tissue and lymph node: 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14
    • lung tissue and lymph node metastasis: 1, 2