TNMplot.com: a web tool for the comparison of gene expression in normal, tumor and metastatic tissues
Bartha, A.; Gyorffy, B.
Show abstract
Genes showing higher expression in either tumor or metastatic tissues can help in better understanding tumor formation, and can serve as biomarkers of progression or as therapy targets with minimal off-target effects. Our goal was to establish an integrated database using available transcriptome-level datasets and to create a web-platform enabling mining of this database by comparing normal, tumor and metastatic data across all genes in real time. We utilized data generated by either gene arrays or RNA-seq. Gene array data were manually selected from NCBI-GEO. RNA sequencing data was downloaded from the TCGA, TARGET, and GTEx repositories. TCGA and TARGET contain predominantly tumor and metastatic samples from adult and pediatric patients, while GTEx samples are from healthy tissues. Statistical significance was computed using Mann-Whitney or Kruskall-Wallis tests. The entire database contains 56,938 samples including 33,520 samples from 3,180 gene chip-based studies (453 metastatic, 29,376 tumorous and 3,691 normal samples), 11,010 samples from TCGA (394 metastatic, 9,886 tumorous and 730 normal), 1,193 samples from TARGET (1 metastatic, 1,180 tumor, 12 normal) and 11,215 normal samples from GTEx. The most consistently up-regulated genes across multiple tumor types were TOP2A (mean FC=7.8), SPP1 (FC=7.0) and CENPA (FC=6.03) and the most consistently down-regulated gene was ADH1B (mean FC=0.15). Validation of differential expression using equally sized training and test sets confirmed reliability of the database in breast, colon, and lung cancer (p<0.0001). The online analysis platform enables unrestricted mining of the database and is accessible at www.tnmplot.com.
Matching journals
The top 7 journals account for 50% of the predicted probability mass.
Similar papers in this journal
- Comprehensive cancer-oriented biobanking resource of human samples for studies of post-zygotic genetic variation involved in cancer predisposition 95%
- The novel microRNAs hsa-miR-nov7 and hsa-miR-nov3 are over-expressed in locally advanced breast cancer 95%
- Molecular signatures for inflammation vary across cancer types and correlate significantly with tumor stage, gender and vital status of patients 94%
Similar papers in this journal
- Development of a Single Molecule Counting Assay to Differentiate Chromophobe Renal Cancer and Oncocytoma in Clinics 96%
- COL7A1 expression improves prognosis prediction for patients with clear cell renal cell carcinoma atop of stage 95%
- Hormone Receptor-status Prediction in Breast Cancer Using Gene Expression Profiles and Their Macroscopic Landscape 95%
Similar papers in this journal
- Novel ratio-metric features enable the identification of new driver genes across cancer types 95%
- Classification models for Invasive Ductal Carcinoma Progression, based on gene expression data-trained supervised machine learning 94%
- Uncovering Hidden Cancer Self-Dependencies through Analysis of shRNA-Level Dependency Scores 94%
Similar papers in this journal
Similar papers in this journal
- BNIP3 upregulation characterizes cancer cell subpopulation with increased fitness and proliferation 95%
- Patient stratification of clear cell renal cell carcinoma using the global transcription factor activity landscape derived from RNA-seq data 95%
- Systems biomedicine of primary and metastatic colorectal cancer reveals potential therapeutic targets 95%
"Similar papers" are the closest papers from that journal in the model's embedding space. They show what the match is built on, but the ranking comes mostly from a classifier over the whole training set, not from these examples alone.