CRUX, a platform for visualising, exploring and analysing cancer genome cohort data
To better understand how tumours develop, identify prognostic biomarkers and find new treatments, researchers have generated vast catalogues of cancer genome data. However, these datasets are complex, so interpreting their important features requires specialized computational skills and analytical t...
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| Published in | NAR genomics and bioinformatics Vol. 6; no. 1; p. lqae003 |
|---|---|
| Main Authors | , , , , , |
| Format | Journal Article |
| Language | English |
| Published |
England
Oxford University Press
01.03.2024
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| Subjects | |
| Online Access | Get full text |
| ISSN | 2631-9268 2631-9268 |
| DOI | 10.1093/nargab/lqae003 |
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| Abstract | To better understand how tumours develop, identify prognostic biomarkers and find new treatments, researchers have generated vast catalogues of cancer genome data. However, these datasets are complex, so interpreting their important features requires specialized computational skills and analytical tools, which presents a significant technical challenge. To address this, we developed CRUX, a platform for exploring genomic data from cancer cohorts. CRUX enables researchers to perform common analyses including cohort comparisons, biomarker discovery, survival analysis, and to create visualisations including oncoplots and lollipop charts. CRUX simplifies cancer genome analysis in several ways: (i) it has an easy-to-use graphical interface; (ii) it enables users to create custom cohorts, as well as analyse precompiled public and private user-created datasets; (iii) it allows analyses to be run locally to address data privacy concerns (though an online version is also available) and (iv) it makes it easy to use additional specialized tools by exporting data in the correct formats. We showcase CRUX’s capabilities with case studies employing different types of cancer genome analysis, demonstrating how it can be used flexibly to generate valuable insights into cancer biology. CRUX is freely available at https://github.com/CCICB/CRUX and https://ccicb.shinyapps.io/crux (DOI: 10.5281/zenodo.8015714). |
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| AbstractList | To better understand how tumours develop, identify prognostic biomarkers and find new treatments, researchers have generated vast catalogues of cancer genome data. However, these datasets are complex, so interpreting their important features requires specialized computational skills and analytical tools, which presents a significant technical challenge. To address this, we developed CRUX, a platform for exploring genomic data from cancer cohorts. CRUX enables researchers to perform common analyses including cohort comparisons, biomarker discovery, survival analysis, and to create visualisations including oncoplots and lollipop charts. CRUX simplifies cancer genome analysis in several ways: (i) it has an easy-to-use graphical interface; (ii) it enables users to create custom cohorts, as well as analyse precompiled public and private user-created datasets; (iii) it allows analyses to be run locally to address data privacy concerns (though an online version is also available) and (iv) it makes it easy to use additional specialized tools by exporting data in the correct formats. We showcase CRUX's capabilities with case studies employing different types of cancer genome analysis, demonstrating how it can be used flexibly to generate valuable insights into cancer biology. CRUX is freely available at https://github.com/CCICB/CRUX and https://ccicb.shinyapps.io/crux (DOI: 10.5281/zenodo.8015714). To better understand how tumours develop, identify prognostic biomarkers and find new treatments, researchers have generated vast catalogues of cancer genome data. However, these datasets are complex, so interpreting their important features requires specialized computational skills and analytical tools, which presents a significant technical challenge. To address this, we developed CRUX, a platform for exploring genomic data from cancer cohorts. CRUX enables researchers to perform common analyses including cohort comparisons, biomarker discovery, survival analysis, and to create visualisations including oncoplots and lollipop charts. CRUX simplifies cancer genome analysis in several ways: (i) it has an easy-to-use graphical interface; (ii) it enables users to create custom cohorts, as well as analyse precompiled public and private user-created datasets; (iii) it allows analyses to be run locally to address data privacy concerns (though an online version is also available) and (iv) it makes it easy to use additional specialized tools by exporting data in the correct formats. We showcase CRUX’s capabilities with case studies employing different types of cancer genome analysis, demonstrating how it can be used flexibly to generate valuable insights into cancer biology. CRUX is freely available at https://github.com/CCICB/CRUX and https://ccicb.shinyapps.io/crux (DOI: 10.5281/zenodo.8015714). To better understand how tumours develop, identify prognostic biomarkers and find new treatments, researchers have generated vast catalogues of cancer genome data. However, these datasets are complex, so interpreting their important features requires specialized computational skills and analytical tools, which presents a significant technical challenge. To address this, we developed CRUX, a platform for exploring genomic data from cancer cohorts. CRUX enables researchers to perform common analyses including cohort comparisons, biomarker discovery, survival analysis, and to create visualisations including oncoplots and lollipop charts. CRUX simplifies cancer genome analysis in several ways: (i) it has an easy-to-use graphical interface; (ii) it enables users to create custom cohorts, as well as analyse precompiled public and private user-created datasets; (iii) it allows analyses to be run locally to address data privacy concerns (though an online version is also available) and (iv) it makes it easy to use additional specialized tools by exporting data in the correct formats. We showcase CRUX’s capabilities with case studies employing different types of cancer genome analysis, demonstrating how it can be used flexibly to generate valuable insights into cancer biology. CRUX is freely available at https://github.com/CCICB/CRUX and https://ccicb.shinyapps.io/crux (DOI: 10.5281/zenodo.8015714). To better understand how tumours develop, identify prognostic biomarkers and find new treatments, researchers have generated vast catalogues of cancer genome data. However, these datasets are complex, so interpreting their important features requires specialized computational skills and analytical tools, which presents a significant technical challenge. To address this, we developed CRUX, a platform for exploring genomic data from cancer cohorts. CRUX enables researchers to perform common analyses including cohort comparisons, biomarker discovery, survival analysis, and to create visualisations including oncoplots and lollipop charts. CRUX simplifies cancer genome analysis in several ways: (i) it has an easy-to-use graphical interface; (ii) it enables users to create custom cohorts, as well as analyse precompiled public and private user-created datasets; (iii) it allows analyses to be run locally to address data privacy concerns (though an online version is also available) and (iv) it makes it easy to use additional specialized tools by exporting data in the correct formats. We showcase CRUX's capabilities with case studies employing different types of cancer genome analysis, demonstrating how it can be used flexibly to generate valuable insights into cancer biology. CRUX is freely available at https://github.com/CCICB/CRUX and https://ccicb.shinyapps.io/crux (DOI: 10.5281/zenodo.8015714).To better understand how tumours develop, identify prognostic biomarkers and find new treatments, researchers have generated vast catalogues of cancer genome data. However, these datasets are complex, so interpreting their important features requires specialized computational skills and analytical tools, which presents a significant technical challenge. To address this, we developed CRUX, a platform for exploring genomic data from cancer cohorts. CRUX enables researchers to perform common analyses including cohort comparisons, biomarker discovery, survival analysis, and to create visualisations including oncoplots and lollipop charts. CRUX simplifies cancer genome analysis in several ways: (i) it has an easy-to-use graphical interface; (ii) it enables users to create custom cohorts, as well as analyse precompiled public and private user-created datasets; (iii) it allows analyses to be run locally to address data privacy concerns (though an online version is also available) and (iv) it makes it easy to use additional specialized tools by exporting data in the correct formats. We showcase CRUX's capabilities with case studies employing different types of cancer genome analysis, demonstrating how it can be used flexibly to generate valuable insights into cancer biology. CRUX is freely available at https://github.com/CCICB/CRUX and https://ccicb.shinyapps.io/crux (DOI: 10.5281/zenodo.8015714). |
| Author | Wong-Erasmus, Marie Cowley, Mark J El-Kamand, Sam Sareen, Heena Becker, Therese M Quinn, Julian M W |
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| Cites_doi | 10.1016/j.ctrv.2012.12.001 10.1038/nature07385 10.1126/scisignal.2004088 10.1093/nar/gkaa423 10.1186/s13073-018-0531-8 10.3389/fnmol.2018.00082 10.1101/gr.239244.118 10.1056/NEJMp1607591 10.12688/f1000research.14197.1 10.1016/j.cell.2014.09.050 10.1038/nprot.2015.105 10.1038/s43018-020-0027-5 10.1158/2159-8290.CD-12-0095 10.1016/j.humpath.2015.09.035 10.1038/nature11412 10.3390/cancers11091388 10.1038/nature12213 10.1038/s41568-020-0290-x 10.1186/s12920-014-0064-y 10.1007/s11060-019-03126-x 10.1038/s41586-020-1969-6 10.1038/ng.2734 10.1093/nar/gkq603 10.1038/s41388-018-0536-1 10.1158/2159-8290.CD-20-1230 10.1007/s00401-010-0645-6 10.3390/cancers14184377 10.1016/j.cell.2013.09.034 10.1111/cas.13696 10.1186/s13059-016-0994-0 10.1093/nar/gky406 10.1155/2017/7082696 10.1038/ng0506-500 |
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| References | Koboldt (2024020117273649200_B36) 2012; 490 Lee (2024020117273649200_B4) 2018; 46 Martínez-Jiménez (2024020117273649200_B17) 2020; 20 Shyr (2024020117273649200_B18) 2014; 7 Chakravarty (2024020117273649200_B24) 2017; 2017 Leong (2024020117273649200_B26) 2019; 38 Shimoi (2024020117273649200_B28) 2018; 109 McLendon (2024020117273649200_B20) 2008; 455 Bücker (2024020117273649200_B30) 2022; 14 Tomczak (2024020117273649200_B6) 2015; 19 Mu (2024020117273649200_B23) 2018; 11 Lawrence (2024020117273649200_B16) 2013; 499 Wang (2024020117273649200_B11) 2010; 38 Crispo (2024020117273649200_B25) 2019; 11 Asch-Kendrick (2024020117273649200_B29) 2016; 48 Gao (2024020117273649200_B14) 2013; 6 Guan (2024020117273649200_B5) 2020; 48 Liu (2024020117273649200_B22) 2019; 142 Cerami (2024020117273649200_B2) 2012; 2 Agrawal (2024020117273649200_B35) 2014; 159 Turner (2024020117273649200_B27) 2013; 39 Degasperi (2024020117273649200_B9) 2020; 1 Campbell (2024020117273649200_B7) 2020; 578 Broad Institute TCGA Genome Data Analysis Center (2024020117273649200_B37) 2016 Yang (2024020117273649200_B12) 2015; 10 Frattini (2024020117273649200_B33) 2013; 45 Tamborero (2024020117273649200_B15) 2018; 10 Mayakonda (2024020117273649200_B8) 2018; 28 Kandoth (2024020117273649200_B10) 2020 McLeod (2024020117273649200_B1) 2021; 11 Ryskalin (2024020117273649200_B19) 2017; 2017 Brennan (2024020117273649200_B34) 2013; 155 Bleeker (2024020117273649200_B21) 2010; 119 Reich (2024020117273649200_B3) 2006; 38 Mularoni (2024020117273649200_B13) 2016; 17 Silva (2024020117273649200_B31) 2018; 7 Grossman (2024020117273649200_B32) 2016; 375 |
| References_xml | – volume: 39 start-page: 541 year: 2013 ident: 2024020117273649200_B27 article-title: Targeting triple negative breast cancer: is p53 the answer? publication-title: Cancer Treat. Rev. doi: 10.1016/j.ctrv.2012.12.001 – volume: 455 start-page: 1061 year: 2008 ident: 2024020117273649200_B20 article-title: Comprehensive genomic characterization defines human glioblastoma genes and core pathways publication-title: Nature doi: 10.1038/nature07385 – volume: 6 start-page: pl1 year: 2013 ident: 2024020117273649200_B14 article-title: Integrative analysis of complex cancer genomics and clinical profiles using the cBioPortal publication-title: Sci. Signal doi: 10.1126/scisignal.2004088 – volume: 48 start-page: W463 year: 2020 ident: 2024020117273649200_B5 article-title: CVCDAP: an integrated platform for molecular and clinical analysis of cancer virtual cohorts publication-title: Nucleic Acids Res. doi: 10.1093/nar/gkaa423 – volume: 10 start-page: 25 year: 2018 ident: 2024020117273649200_B15 article-title: Cancer genome interpreter annotates the biological and clinical relevance of tumor alterations publication-title: Genome Medicine doi: 10.1186/s13073-018-0531-8 – volume: 11 start-page: 82 year: 2018 ident: 2024020117273649200_B23 article-title: The IDH1 mutation-induced oncometabolite, 2-hydroxyglutarate, may affect DNA methylation and expression of PD-L1 in gliomas publication-title: Front Mol. Neurosci. doi: 10.3389/fnmol.2018.00082 – volume: 28 start-page: 1747 year: 2018 ident: 2024020117273649200_B8 article-title: Maftools: efficient and comprehensive analysis of somatic variants in cancer publication-title: Genome Res. doi: 10.1101/gr.239244.118 – volume: 2017 start-page: PO.17.00011 year: 2017 ident: 2024020117273649200_B24 article-title: OncoKB: a precision oncology knowledge base publication-title: JCO Precis. Oncol. – volume: 375 start-page: 1109 year: 2016 ident: 2024020117273649200_B32 article-title: Toward a shared vision for cancer genomic data publication-title: N. Engl. J. Med. doi: 10.1056/NEJMp1607591 – volume-title: Broad Institute of MIT and Harvard (ed.) year: 2016 ident: 2024020117273649200_B37 – volume: 7 start-page: 439 year: 2018 ident: 2024020117273649200_B31 article-title: TCGAbiolinksGUI: a graphical user interface to analyze cancer molecular and clinical data [version 1; peer review: 1 approved, 1 approved with reservations] publication-title: F1000Research doi: 10.12688/f1000research.14197.1 – year: 2020 ident: 2024020117273649200_B10 – volume: 159 start-page: 676 year: 2014 ident: 2024020117273649200_B35 article-title: Integrated genomic characterization of papillary thyroid carcinoma publication-title: Cell doi: 10.1016/j.cell.2014.09.050 – volume: 19 start-page: A68 year: 2015 ident: 2024020117273649200_B6 article-title: The Cancer Genome Atlas (TCGA): an immeasurable source of knowledge publication-title: Contemp. Oncol. (Poznan, Poland) – volume: 10 start-page: 1556 year: 2015 ident: 2024020117273649200_B12 article-title: Genomic variant annotation and prioritization with ANNOVAR and wANNOVAR publication-title: Nat. Protoc. doi: 10.1038/nprot.2015.105 – volume: 1 start-page: 249 year: 2020 ident: 2024020117273649200_B9 article-title: A practical framework and online tool for mutational signature analyses show intertissue variation and driver dependencies publication-title: Nature Cancer doi: 10.1038/s43018-020-0027-5 – volume: 2 start-page: 401 year: 2012 ident: 2024020117273649200_B2 article-title: The cBio cancer genomics portal: an open platform for exploring multidimensional cancer genomics data publication-title: Cancer Discov. doi: 10.1158/2159-8290.CD-12-0095 – volume: 48 start-page: 37 year: 2016 ident: 2024020117273649200_B29 article-title: The role of GATA3 in breast carcinomas: a review publication-title: Hum. Pathol. doi: 10.1016/j.humpath.2015.09.035 – volume: 490 start-page: 61 year: 2012 ident: 2024020117273649200_B36 article-title: Comprehensive molecular portraits of human breast tumours publication-title: Nature doi: 10.1038/nature11412 – volume: 11 start-page: 1388 year: 2019 ident: 2024020117273649200_B25 article-title: BRAF inhibitors in thyroid cancer: clinical impact, mechanisms of resistance and future perspectives publication-title: Cancers (Basel) doi: 10.3390/cancers11091388 – volume: 499 start-page: 214 year: 2013 ident: 2024020117273649200_B16 article-title: Mutational heterogeneity in cancer and the search for new cancer-associated genes publication-title: Nature doi: 10.1038/nature12213 – volume: 20 start-page: 555 year: 2020 ident: 2024020117273649200_B17 article-title: A compendium of mutational cancer driver genes publication-title: Nat. Rev. Cancer doi: 10.1038/s41568-020-0290-x – volume: 7 start-page: 64 year: 2014 ident: 2024020117273649200_B18 article-title: FLAGS, frequently mutated genes in public exomes publication-title: BMC Med. Genomics doi: 10.1186/s12920-014-0064-y – volume: 142 start-page: 423 year: 2019 ident: 2024020117273649200_B22 article-title: SPINT2 is hypermethylated in both IDH1 mutated and wild-type glioblastomas, and exerts tumor suppression via reduction of c-met activation publication-title: J. Neurooncol. doi: 10.1007/s11060-019-03126-x – volume: 578 start-page: 82 year: 2020 ident: 2024020117273649200_B7 article-title: Pan-cancer analysis of whole genomes publication-title: Nature doi: 10.1038/s41586-020-1969-6 – volume: 45 start-page: 1141 year: 2013 ident: 2024020117273649200_B33 article-title: The integrated landscape of driver genomic alterations in glioblastoma publication-title: Nat. Genet. doi: 10.1038/ng.2734 – volume: 38 start-page: e164 year: 2010 ident: 2024020117273649200_B11 article-title: ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data publication-title: Nucleic Acids Res. doi: 10.1093/nar/gkq603 – volume: 38 start-page: 1661 year: 2019 ident: 2024020117273649200_B26 article-title: Deep multi-region whole-genome sequencing reveals heterogeneity and gene-by-environment interactions in treatment-naive, metastatic lung cancer publication-title: Oncogene doi: 10.1038/s41388-018-0536-1 – volume: 11 start-page: 1082 year: 2021 ident: 2024020117273649200_B1 article-title: St. Jude Cloud: a pediatric cancer genomic data-sharing ecosystem publication-title: Cancer Discov. doi: 10.1158/2159-8290.CD-20-1230 – volume: 119 start-page: 487 year: 2010 ident: 2024020117273649200_B21 article-title: The prognostic IDH1(R132) mutation is associated with reduced NADP+-dependent IDH activity in glioblastoma publication-title: Acta Neuropathol. doi: 10.1007/s00401-010-0645-6 – volume: 14 start-page: 4377 year: 2022 ident: 2024020117273649200_B30 article-title: CDH1 (E-cadherin) gene methylation in Human breast cancer: critical appraisal of a long and twisted story publication-title: Cancers (Basel) doi: 10.3390/cancers14184377 – volume: 155 start-page: 462 year: 2013 ident: 2024020117273649200_B34 article-title: The somatic genomic landscape of glioblastoma publication-title: Cell doi: 10.1016/j.cell.2013.09.034 – volume: 109 start-page: 2558 year: 2018 ident: 2024020117273649200_B28 article-title: PIK3CA mutation profiling in patients with breast cancer, using a highly sensitive detection system publication-title: Cancer Sci. doi: 10.1111/cas.13696 – volume: 17 start-page: 128 year: 2016 ident: 2024020117273649200_B13 article-title: OncodriveFML: a general framework to identify coding and non-coding regions with cancer driver mutations publication-title: Genome Biol. doi: 10.1186/s13059-016-0994-0 – volume: 46 start-page: W102 year: 2018 ident: 2024020117273649200_B4 article-title: Mutalisk: a web-based somatic MUTation AnaLyIS toolKit for genomic, transcriptional and epigenomic signatures publication-title: Nucleic Acids Res. doi: 10.1093/nar/gky406 – volume: 2017 start-page: 7082696 year: 2017 ident: 2024020117273649200_B19 article-title: mTOR-dependent cell proliferation in the brain publication-title: Biomed. Res. Int. doi: 10.1155/2017/7082696 – volume: 38 start-page: 500 year: 2006 ident: 2024020117273649200_B3 article-title: GenePattern 2.0 publication-title: Nat. Genet. doi: 10.1038/ng0506-500 |
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| Snippet | To better understand how tumours develop, identify prognostic biomarkers and find new treatments, researchers have generated vast catalogues of cancer genome... To better understand how tumours develop, identify prognostic biomarkers and find new treatments, researchers have generated vast catalogues of cancer genome... |
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| SubjectTerms | Biomarkers Cancer Genomes Genomic analysis Survival analysis |
| Title | CRUX, a platform for visualising, exploring and analysing cancer genome cohort data |
| URI | https://www.ncbi.nlm.nih.gov/pubmed/38304083 https://www.proquest.com/docview/3170909017 https://www.proquest.com/docview/2929127871 https://pubmed.ncbi.nlm.nih.gov/PMC10833466 |
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