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 inNAR genomics and bioinformatics Vol. 6; no. 1; p. lqae003
Main Authors El-Kamand, Sam, Quinn, Julian M W, Sareen, Heena, Becker, Therese M, Wong-Erasmus, Marie, Cowley, Mark J
Format Journal Article
LanguageEnglish
Published England Oxford University Press 01.03.2024
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ISSN2631-9268
2631-9268
DOI10.1093/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).
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
Volume 6
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