UALCAN: An update to the integrated cancer data analysis platform
Cancer genomic, transcriptomic, and proteomic profiling has generated extensive data that necessitate the development of tools for its analysis and dissemination. We developed UALCAN to provide a portal for easy exploring, analyzing, and visualizing these data, allowing users to integrate the data t...
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| Published in: | Neoplasia (New York, N.Y.) Vol. 25; pp. 18 - 27 |
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| Main Authors: | , , , , , , , , , , , |
| Format: | Journal Article |
| Language: | English |
| Published: |
United States
Elsevier Inc
01.03.2022
Neoplasia Press Elsevier |
| Subjects: | |
| ISSN: | 1476-5586, 1522-8002, 1476-5586 |
| Online Access: | Get full text |
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| Abstract | Cancer genomic, transcriptomic, and proteomic profiling has generated extensive data that necessitate the development of tools for its analysis and dissemination. We developed UALCAN to provide a portal for easy exploring, analyzing, and visualizing these data, allowing users to integrate the data to better understand the gene, proteins, and pathways perturbed in cancer and make discoveries. UALCAN web portal enables analyzing and delivering cancer transcriptome, proteomics, and patient survival data to the cancer research community. With data obtained from The Cancer Genome Atlas (TCGA) project, UALCAN has enabled users to evaluate protein-coding gene expression and its impact on patient survival across 33 types of cancers. The web portal has been used extensively since its release and received immense popularity, underlined by its usage from cancer researchers in more than 100 countries. The present manuscript highlights the task we have undertaken and updates that we have made to UALCAN since its release in 2017. Extensive user feedback motivated us to expand the resource by including data on a) microRNAs (miRNAs), long non-coding RNAs (lncRNAs), and promoter DNA methylation from TCGA and b) mass spectrometry-based proteomics from the Clinical Proteomic Tumor Analysis Consortium (CPTAC). UALCAN provides easy access to pre-computed, tumor subgroup-based gene/protein expression, promoter DNA methylation status, and Kaplan-Meier survival analyses. It also provides new visualization features to comprehend and integrate observations and aids in generating hypotheses for testing. UALCAN is accessible at http://ualcan.path.uab.edu |
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| AbstractList | Cancer genomic, transcriptomic, and proteomic profiling has generated extensive data that necessitate the development of tools for its analysis and dissemination. We developed UALCAN to provide a portal for easy exploring, analyzing, and visualizing these data, allowing users to integrate the data to better understand the gene, proteins, and pathways perturbed in cancer and make discoveries. UALCAN web portal enables analyzing and delivering cancer transcriptome, proteomics, and patient survival data to the cancer research community. With data obtained from The Cancer Genome Atlas (TCGA) project, UALCAN has enabled users to evaluate protein-coding gene expression and its impact on patient survival across 33 types of cancers. The web portal has been used extensively since its release and received immense popularity, underlined by its usage from cancer researchers in more than 100 countries. The present manuscript highlights the task we have undertaken and updates that we have made to UALCAN since its release in 2017. Extensive user feedback motivated us to expand the resource by including data on a) microRNAs (miRNAs), long non-coding RNAs (lncRNAs), and promoter DNA methylation from TCGA and b) mass spectrometry-based proteomics from the Clinical Proteomic Tumor Analysis Consortium (CPTAC). UALCAN provides easy access to pre-computed, tumor subgroup-based gene/protein expression, promoter DNA methylation status, and Kaplan-Meier survival analyses. It also provides new visualization features to comprehend and integrate observations and aids in generating hypotheses for testing. UALCAN is accessible at http://ualcan.path.uab.edu Cancer genomic, transcriptomic, and proteomic profiling has generated extensive data that necessitate the development of tools for its analysis and dissemination. We developed UALCAN to provide a portal for easy exploring, analyzing, and visualizing these data, allowing users to integrate the data to better understand the gene, proteins, and pathways perturbed in cancer and make discoveries. UALCAN web portal enables analyzing and delivering cancer transcriptome, proteomics, and patient survival data to the cancer research community. With data obtained from The Cancer Genome Atlas (TCGA) project, UALCAN has enabled users to evaluate protein-coding gene expression and its impact on patient survival across 33 types of cancers. The web portal has been used extensively since its release and received immense popularity, underlined by its usage from cancer researchers in more than 100 countries. The present manuscript highlights the task we have undertaken and updates that we have made to UALCAN since its release in 2017. Extensive user feedback motivated us to expand the resource by including data on a) microRNAs (miRNAs), long non-coding RNAs (lncRNAs), and promoter DNA methylation from TCGA and b) mass spectrometry-based proteomics from the Clinical Proteomic Tumor Analysis Consortium (CPTAC). UALCAN provides easy access to pre-computed, tumor subgroup-based gene/protein expression, promoter DNA methylation status, and Kaplan-Meier survival analyses. It also provides new visualization features to comprehend and integrate observations and aids in generating hypotheses for testing. UALCAN is accessible at http://ualcan.path.uab.edu. Cancer genomic, transcriptomic, and proteomic profiling has generated extensive data that necessitate the development of tools for its analysis and dissemination. We developed UALCAN to provide a portal for easy exploring, analyzing, and visualizing these data, allowing users to integrate the data to better understand the gene, proteins, and pathways perturbed in cancer and make discoveries. UALCAN web portal enables analyzing and delivering cancer transcriptome, proteomics, and patient survival data to the cancer research community. With data obtained from The Cancer Genome Atlas (TCGA) project, UALCAN has enabled users to evaluate protein-coding gene expression and its impact on patient survival across 33 types of cancers. The web portal has been used extensively since its release and received immense popularity, underlined by its usage from cancer researchers in more than 100 countries. The present manuscript highlights the task we have undertaken and updates that we have made to UALCAN since its release in 2017. Extensive user feedback motivated us to expand the resource by including data on a) microRNAs (miRNAs), long non-coding RNAs (lncRNAs), and promoter DNA methylation from TCGA and b) mass spectrometry-based proteomics from the Clinical Proteomic Tumor Analysis Consortium (CPTAC). UALCAN provides easy access to pre-computed, tumor subgroup-based gene/protein expression, promoter DNA methylation status, and Kaplan-Meier survival analyses. It also provides new visualization features to comprehend and integrate observations and aids in generating hypotheses for testing. UALCAN is accessible at http://ualcan.path.uab.edu.Cancer genomic, transcriptomic, and proteomic profiling has generated extensive data that necessitate the development of tools for its analysis and dissemination. We developed UALCAN to provide a portal for easy exploring, analyzing, and visualizing these data, allowing users to integrate the data to better understand the gene, proteins, and pathways perturbed in cancer and make discoveries. UALCAN web portal enables analyzing and delivering cancer transcriptome, proteomics, and patient survival data to the cancer research community. With data obtained from The Cancer Genome Atlas (TCGA) project, UALCAN has enabled users to evaluate protein-coding gene expression and its impact on patient survival across 33 types of cancers. The web portal has been used extensively since its release and received immense popularity, underlined by its usage from cancer researchers in more than 100 countries. The present manuscript highlights the task we have undertaken and updates that we have made to UALCAN since its release in 2017. Extensive user feedback motivated us to expand the resource by including data on a) microRNAs (miRNAs), long non-coding RNAs (lncRNAs), and promoter DNA methylation from TCGA and b) mass spectrometry-based proteomics from the Clinical Proteomic Tumor Analysis Consortium (CPTAC). UALCAN provides easy access to pre-computed, tumor subgroup-based gene/protein expression, promoter DNA methylation status, and Kaplan-Meier survival analyses. It also provides new visualization features to comprehend and integrate observations and aids in generating hypotheses for testing. UALCAN is accessible at http://ualcan.path.uab.edu. |
| Author | Karthikeyan, Santhosh Kumar Korla, Praveen Kumar Netto, George J. Manne, Upender Chandrashekar, Darshan Shimoga Qin, Zhaohui S. Kumar, Sidharth Shovon, Ahmedur Rahman Creighton, Chad J. Patel, Henalben Athar, Mohammad Varambally, Sooryanarayana |
| Author_xml | – sequence: 1 givenname: Darshan Shimoga surname: Chandrashekar fullname: Chandrashekar, Darshan Shimoga email: dshimogachandrasheka@uabmc.edu organization: Department of Pathology, University of Alabama at Birmingham, Birmingham, AL, USA – sequence: 2 givenname: Santhosh Kumar orcidid: 0000-0003-2796-8110 surname: Karthikeyan fullname: Karthikeyan, Santhosh Kumar organization: Department of Pathology, University of Alabama at Birmingham, Birmingham, AL, USA – sequence: 3 givenname: Praveen Kumar surname: Korla fullname: Korla, Praveen Kumar organization: Department of Pathology, University of Alabama at Birmingham, Birmingham, AL, USA – sequence: 4 givenname: Henalben surname: Patel fullname: Patel, Henalben organization: Department of Pathology, University of Alabama at Birmingham, Birmingham, AL, USA – sequence: 5 givenname: Ahmedur Rahman orcidid: 0000-0002-5718-4977 surname: Shovon fullname: Shovon, Ahmedur Rahman organization: Department of Computer science, University of Alabama at Birmingham, Birmingham, AL, USA – sequence: 6 givenname: Mohammad surname: Athar fullname: Athar, Mohammad organization: O'Neal Comprehensive Cancer Center, University of Alabama at Birmingham, Birmingham, AL, USA – sequence: 7 givenname: George J. surname: Netto fullname: Netto, George J. organization: Department of Pathology, University of Alabama at Birmingham, Birmingham, AL, USA – sequence: 8 givenname: Zhaohui S. orcidid: 0000-0002-1583-146X surname: Qin fullname: Qin, Zhaohui S. organization: Department of Biostatistics and Bioinformatics, Emory University, Atlanta, GA 30322, USA – sequence: 9 givenname: Sidharth surname: Kumar fullname: Kumar, Sidharth organization: Department of Computer science, University of Alabama at Birmingham, Birmingham, AL, USA – sequence: 10 givenname: Upender orcidid: 0000-0002-1545-3032 surname: Manne fullname: Manne, Upender organization: Department of Pathology, University of Alabama at Birmingham, Birmingham, AL, USA – sequence: 11 givenname: Chad J. orcidid: 0000-0002-6090-703X surname: Creighton fullname: Creighton, Chad J. organization: Department of Medicine and Dan L. Duncan Comprehensive Cancer Center, Baylor College of Medicine, Houston, TX, USA – sequence: 12 givenname: Sooryanarayana surname: Varambally fullname: Varambally, Sooryanarayana email: svarambally@uabmc.edu organization: Department of Pathology, University of Alabama at Birmingham, Birmingham, AL, USA |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/35078134$$D View this record in MEDLINE/PubMed |
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