arrayMap - Genomic Array Data for Cancer CNV Profiles
Names
More detailed information about this field from each metasource.
arrayMap - Genomic Array Data for Cancer CNV Profiles
metasource: Fairsharing.org
version: FAIRsharing.org: arrayMap; arrayMap - Genomic Array Data for Cancer CNV Profiles; DOI: https://doi.org/10.25504/FAIRsharing.1fbc5y; Last edited: May 4, 2021, 8:16 a.m.; Last accessed: Jan 03 2022 7:06 p.m.
arrayMap
metasource: Fairsharing.org
version: FAIRsharing.org: arrayMap; arrayMap - Genomic Array Data for Cancer CNV Profiles; DOI: https://doi.org/10.25504/FAIRsharing.1fbc5y; Last edited: May 4, 2021, 8:16 a.m.; Last accessed: Jan 03 2022 7:06 p.m.
metasource: re3data.org
version: re3data.org: arrayMap; editing status 2021-01-20; re3data.org - Registry of Research Data Repositories. http://doi.org/10.17616/R3X78M last accessed: 2022-11-04
metasource: bio.tools
version: extracted_at: 2022-11-04T11:31:12.319463
ArrayMap
metasource: Nucleic Acid Research database catalogue
version: extracted_at: 2022-11-04T11:16:25.468657
arraymap
metasource: bio.tools
version: extracted_at: 2022-11-04T11:31:12.319463
Names
More detailed information about this field from each metasource.
arrayMap - Genomic Array Data for Cancer CNV Profiles
metasource: Fairsharing.orgversion: FAIRsharing.org: arrayMap; arrayMap - Genomic Array Data for Cancer CNV Profiles; DOI: https://doi.org/10.25504/FAIRsharing.1fbc5y; Last edited: May 4, 2021, 8:16 a.m.; Last accessed: Jan 03 2022 7:06 p.m.
arrayMap
metasource: Fairsharing.orgversion: FAIRsharing.org: arrayMap; arrayMap - Genomic Array Data for Cancer CNV Profiles; DOI: https://doi.org/10.25504/FAIRsharing.1fbc5y; Last edited: May 4, 2021, 8:16 a.m.; Last accessed: Jan 03 2022 7:06 p.m.
metasource: re3data.org
version: re3data.org: arrayMap; editing status 2021-01-20; re3data.org - Registry of Research Data Repositories. http://doi.org/10.17616/R3X78M last accessed: 2022-11-04
metasource: bio.tools
version: extracted_at: 2022-11-04T11:31:12.319463
ArrayMap
metasource: Nucleic Acid Research database catalogueversion: extracted_at: 2022-11-04T11:16:25.468657
arraymap
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:31:12.319463
Other names: arrayMap, ArrayMap, arraymap
Names
More detailed information about this field from each metasource.
arrayMap - Genomic Array Data for Cancer CNV Profiles
metasource: Fairsharing.orgversion: FAIRsharing.org: arrayMap; arrayMap - Genomic Array Data for Cancer CNV Profiles; DOI: https://doi.org/10.25504/FAIRsharing.1fbc5y; Last edited: May 4, 2021, 8:16 a.m.; Last accessed: Jan 03 2022 7:06 p.m.
arrayMap
metasource: Fairsharing.orgversion: FAIRsharing.org: arrayMap; arrayMap - Genomic Array Data for Cancer CNV Profiles; DOI: https://doi.org/10.25504/FAIRsharing.1fbc5y; Last edited: May 4, 2021, 8:16 a.m.; Last accessed: Jan 03 2022 7:06 p.m.
metasource: re3data.org
version: re3data.org: arrayMap; editing status 2021-01-20; re3data.org - Registry of Research Data Repositories. http://doi.org/10.17616/R3X78M last accessed: 2022-11-04
metasource: bio.tools
version: extracted_at: 2022-11-04T11:31:12.319463
ArrayMap
metasource: Nucleic Acid Research database catalogueversion: extracted_at: 2022-11-04T11:16:25.468657
arraymap
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:31:12.319463
Part of the Progenetix project, the arrayMap database facilitates the study of the genetics of human cancer. The Progenetix project provides the data customisation and visualization tools to mine the available data. The arrayMap database is developed by the group "Theoretical Cytogenetics and Oncogenomics" at the Department of Molecular Life Sciences of the University of Zurich.
Description
More detailed information about this field from each metasource.
Part of the Progenetix project, the arrayMap database facilitates the study of the genetics of human cancer. The Progenetix project provides the data customisation and visualization tools to mine the available data. The arrayMap database is developed by the group "Theoretical Cytogenetics and Oncogenomics" at the Department of Molecular Life Sciences of the University of Zurich.
metasource: Fairsharing.orgversion: FAIRsharing.org: arrayMap; arrayMap - Genomic Array Data for Cancer CNV Profiles; DOI: https://doi.org/10.25504/FAIRsharing.1fbc5y; Last edited: May 4, 2021, 8:16 a.m.; Last accessed: Jan 03 2022 7:06 p.m.
arrayMap is a curated reference database and bioinformatics resource targeting copy number profiling data in human cancer. The arrayMap database provides an entry point for meta-analysis and systems level data integration of high-resolution oncogenomic CNA data.
metasource: Nucleic Acid Research database catalogueversion: extracted_at: 2022-11-04T11:16:25.468657
arrayMap is a repository of cancer genome profiling data. Original) from primary repositories (e.g. NCBI GEO, EBI ArrayExpress, TCGA) is re-processed and annotated for metadata. Unique visualization of the processed data allows critical evaluation of data quality and genome information. Structured metadata provides easy access to summary statistics, with a focus on copy number aberrations in cancer entities.
metasource: re3data.orgversion: re3data.org: arrayMap; editing status 2021-01-20; re3data.org - Registry of Research Data Repositories. http://doi.org/10.17616/R3X78M last accessed: 2022-11-04
A curated reference database and bioinformatics resource targeting copy number profiling data in human cancer. The arrayMap database provides an entry point for meta-analysis and systems level data integration of high-resolution oncogenomic CNA data. The arrayMap resource represents the part of the Progenetix project for which direct access to source data (i.e. probe-specific genomic array read-outs) has been available during data curation.
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:31:12.319463
Webpage:
http://arraymap.orgWebpage
More detailed information about this field from each metasource.
http://arraymap.org
metasource: Fairsharing.orgversion: FAIRsharing.org: arrayMap; arrayMap - Genomic Array Data for Cancer CNV Profiles; DOI: https://doi.org/10.25504/FAIRsharing.1fbc5y; Last edited: May 4, 2021, 8:16 a.m.; Last accessed: Jan 03 2022 7:06 p.m.
metasource: bio.tools
version: extracted_at: 2022-11-04T11:31:12.319463
https://arraymap.progenetix.org/
metasource: Nucleic Acid Research database catalogueversion: extracted_at: 2022-11-04T11:16:25.468657
metasource: re3data.org
version: re3data.org: arrayMap; editing status 2021-01-20; re3data.org - Registry of Research Data Repositories. http://doi.org/10.17616/R3X78M last accessed: 2022-11-04
Licence:
Name: Creative Commons Attribution-NonCommercial-NoDerivs 2.5 Switzerland (CC BY-NC-ND 2.5 CH)Licence name
More detailed information about this field from each metasource.
Creative Commons Attribution-NonCommercial-NoDerivs 2.5 Switzerland (CC BY-NC-ND 2.5 CH)
metasource: Fairsharing.orgversion: FAIRsharing.org: arrayMap; arrayMap - Genomic Array Data for Cancer CNV Profiles; DOI: https://doi.org/10.25504/FAIRsharing.1fbc5y; Last edited: May 4, 2021, 8:16 a.m.; Last accessed: Jan 03 2022 7:06 p.m.
CC
metasource: re3data.orgversion: re3data.org: arrayMap; editing status 2021-01-20; re3data.org - Registry of Research Data Repositories. http://doi.org/10.17616/R3X78M last accessed: 2022-11-04
CC-BY-SA-4.0
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:31:12.319463
Licence URL
More detailed information about this field from each metasource.
https://creativecommons.org/licenses/by-nc-nd/2.5/ch/
metasource: Fairsharing.orgversion: FAIRsharing.org: arrayMap; arrayMap - Genomic Array Data for Cancer CNV Profiles; DOI: https://doi.org/10.25504/FAIRsharing.1fbc5y; Last edited: May 4, 2021, 8:16 a.m.; Last accessed: Jan 03 2022 7:06 p.m.
https://creativecommons.org/licenses/by-sa/4.0/
metasource: re3data.orgversion: re3data.org: arrayMap; editing status 2021-01-20; re3data.org - Registry of Research Data Repositories. http://doi.org/10.17616/R3X78M last accessed: 2022-11-04
Publications:
Publications
More detailed information about this field from each metasource.
Chromothripsis-like patterns are recurring but heterogeneously distributed features in a survey of 22,347 cancer genome screens
PMID: 24476156
metasource: Fairsharing.org
version: FAIRsharing.org: arrayMap; arrayMap - Genomic Array Data for Cancer CNV Profiles; DOI: https://doi.org/10.25504/FAIRsharing.1fbc5y; Last edited: May 4, 2021, 8:16 a.m.; Last accessed: Jan 03 2022 7:06 p.m.
The SIB Swiss Institute of Bioinformatics' resources: focus on curated databases
PMID: 26615188
metasource: Fairsharing.org
version: FAIRsharing.org: arrayMap; arrayMap - Genomic Array Data for Cancer CNV Profiles; DOI: https://doi.org/10.25504/FAIRsharing.1fbc5y; Last edited: May 4, 2021, 8:16 a.m.; Last accessed: Jan 03 2022 7:06 p.m.
arrayMap: a reference resource for genomic copy number imbalances in human malignancies
PMID: 22629346
metasource: Fairsharing.org
version: FAIRsharing.org: arrayMap; arrayMap - Genomic Array Data for Cancer CNV Profiles; DOI: https://doi.org/10.25504/FAIRsharing.1fbc5y; Last edited: May 4, 2021, 8:16 a.m.; Last accessed: Jan 03 2022 7:06 p.m.
arrayMap 2014: an updated cancer genome resource
PMID: 25428357
metasource: Fairsharing.org
version: FAIRsharing.org: arrayMap; arrayMap - Genomic Array Data for Cancer CNV Profiles; DOI: https://doi.org/10.25504/FAIRsharing.1fbc5y; Last edited: May 4, 2021, 8:16 a.m.; Last accessed: Jan 03 2022 7:06 p.m.
http://dx.doi.org/10.1093/nar/gku1123
metasource: Nucleic Acid Research database catalogue
version: extracted_at: 2022-11-04T11:16:25.468657
metasource: bio.tools
version: extracted_at: 2022-11-04T11:31:12.319463
Publications
More detailed information about this field from each metasource.
Chromothripsis-like patterns are recurring but heterogeneously distributed features in a survey of 22,347 cancer genome screens
PMID: 24476156
metasource: Fairsharing.org
version: FAIRsharing.org: arrayMap; arrayMap - Genomic Array Data for Cancer CNV Profiles; DOI: https://doi.org/10.25504/FAIRsharing.1fbc5y; Last edited: May 4, 2021, 8:16 a.m.; Last accessed: Jan 03 2022 7:06 p.m.
The SIB Swiss Institute of Bioinformatics' resources: focus on curated databases
PMID: 26615188
metasource: Fairsharing.org
version: FAIRsharing.org: arrayMap; arrayMap - Genomic Array Data for Cancer CNV Profiles; DOI: https://doi.org/10.25504/FAIRsharing.1fbc5y; Last edited: May 4, 2021, 8:16 a.m.; Last accessed: Jan 03 2022 7:06 p.m.
arrayMap: a reference resource for genomic copy number imbalances in human malignancies
PMID: 22629346
metasource: Fairsharing.org
version: FAIRsharing.org: arrayMap; arrayMap - Genomic Array Data for Cancer CNV Profiles; DOI: https://doi.org/10.25504/FAIRsharing.1fbc5y; Last edited: May 4, 2021, 8:16 a.m.; Last accessed: Jan 03 2022 7:06 p.m.
arrayMap 2014: an updated cancer genome resource
PMID: 25428357
metasource: Fairsharing.org
version: FAIRsharing.org: arrayMap; arrayMap - Genomic Array Data for Cancer CNV Profiles; DOI: https://doi.org/10.25504/FAIRsharing.1fbc5y; Last edited: May 4, 2021, 8:16 a.m.; Last accessed: Jan 03 2022 7:06 p.m.
http://dx.doi.org/10.1093/nar/gku1123
metasource: Nucleic Acid Research database catalogueversion: extracted_at: 2022-11-04T11:16:25.468657
metasource: bio.tools
version: extracted_at: 2022-11-04T11:31:12.319463
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Chromothripsis-like patterns are recurring but heterogeneously distributed features in a survey of 22,347 cancer genome screens
PubMed citations: 45.
45 articles citing: Chromothripsis-like patterns are recurring but heterogeneously distributed features in a survey of 22,347 cancer genome screens
Tumor Junction Burden and Antigen Presentation as Predictors of Survival in Mesothelioma Treated With Immune Checkpoint Inhibitors. PMID:34800701
Gene Duplication and Gene Fusion Are Important Drivers of Tumourigenesis during Cancer Evolution. PMID:34573358
The Progenetix oncogenomic resource in 2021. PMID:34272855
Chromothripsis-Explosion in Genetic Science. PMID:34064429
Genetic alterations associated with multiple primary malignancies. PMID:34057285
Mechanistic origins of diverse genome rearrangements in cancer. PMID:33824062
Inflammatory Breast Cancer: Clinical Implications of Genomic Alterations and Mutational Profiling. PMID:33007869
Multiple Chromoanasynthesis in a Rare Case of Sporadic Renal Leiomyosarcoma: A Case Report. PMID:32974204
Postmortem Examination of an Aggressive Case of Medullary Thyroid Carcinoma Characterized by Catastrophic Genomic Abnormalities. PMID:32913965
Integrative genomics approach identifies molecular features associated with early-stage ovarian carcinoma histotypes. PMID:32409713
The landscape of chromothripsis across adult cancer types. PMID:32385320
The Landscape of Somatic Copy Number Alterations in Head and Neck Squamous Cell Carcinoma. PMID:32226775
Chromosomal rearrangements and their neoantigenic potential in mesothelioma. PMID:32206575
Chromothripsis and telomere crisis: engines of genome instability. PMID:32151946
Reduced SKP1 Expression Induces Chromosome Instability through Aberrant Cyclin E1 Protein Turnover. PMID:32106628
Micronucleus Assay: The State of Art, and Future Directions. PMID:32102335
Comprehensive analysis of chromothripsis in 2,658 human cancers using whole-genome sequencing. PMID:32025003
Chromoanagenesis: a piece of the macroevolution scenario. PMID:32010222
Comprehensive identification and characterization of somatic copy number alterations in triple‑negative breast cancer. PMID:31894314
On the Complexity of Mechanisms and Consequences of Chromothripsis: An Update. PMID:31114609
Genome-wide DNA copy number analysis and targeted transcriptional analysis of canine histiocytic malignancies identifies diagnostic signatures and highlights disruption of spindle assembly complex. PMID:31011867
Chromoanagenesis: cataclysms behind complex chromosomal rearrangements. PMID:30805029
Neoantigenic Potential of Complex Chromosomal Rearrangements in Mesothelioma. PMID:30316012
Genome-wide multi-omics profiling of the 8p11-p12 amplicon in breast carcinoma. PMID:29844878
Chromosomal rearrangements in uveal melanoma: Chromothripsis. PMID:29726589
Chromothripsis in acute myeloid leukemia: biological features and impact on survival. PMID:29472722
Identifying simultaneous rearrangements in cancer genomes. PMID:29186385
Comprehensive Genomic Profiling of a Rare Thyroid Follicular Dendritic Cell Sarcoma. PMID:28975018
New Insights in the Cytogenetic Practice: Karyotypic Chaos, Non-Clonal Chromosomal Alterations and Chromosomal Instability in Human Cancer and Therapy Response. PMID:28587191
TP53 Mutations in Breast and Ovarian Cancer. PMID:27815305
Genomewide copy number analysis of Müllerian adenosarcoma identified chromosomal instability in the aggressive subgroup. PMID:27255164
CTLPScanner: a web server for chromothripsis-like pattern detection. PMID:27185889
From Telomere Crisis via Dicentric Chromosomes to Kataegis and Chromothripsis. PMID:27022325
Chromothripsis after Stumbling through DNA Replication. PMID:26997940
Genome-Wide DNA Copy Number Analysis of Acute Lymphoblastic Leukemia Identifies New Genetic Markers Associated with Clinical Outcome. PMID:26872047
Chromothripsis-like chromosomal rearrangements induced by ionizing radiation using proton microbeam irradiation system. PMID:26862731
A cultured approach to canine urothelial carcinoma: molecular characterization of five cell lines. PMID:26401343
Combined Analysis of SNP Array Data Identifies Novel CNV Candidates and Pathways in Ependymoma and Mesothelioma. PMID:26185765
Error-Prone Repair of DNA Double-Strand Breaks. PMID:26033759
Genomic instability of osteosarcoma cell lines in culture: impact on the prediction of metastasis relevant genes. PMID:25992885
Catastrophic chromosomal restructuring during genome elimination in plants. PMID:25977984
Deep sequencing and SNP array analyses of pediatric T-cell acute lymphoblastic leukemia reveal NOTCH1 mutations in minor subclones and a high incidence of uniparental isodisomies affecting CDKN2A. PMID:25903014
Canine urothelial carcinoma: genomically aberrant and comparatively relevant. PMID:25783786
New concepts in breast cancer genomics and genetics. PMID:25606588
arrayMap 2014: an updated cancer genome resource. PMID:25428357 -
The SIB Swiss Institute of Bioinformatics' resources: focus on curated databases
PubMed citations: 27.
27 articles citing: The SIB Swiss Institute of Bioinformatics' resources: focus on curated databases
The Cancer Research Database (CRDB): Integrated Platform to Gain Statistical Insight Into the Correlation Between Cancer and COVID-19. PMID:35430561
Systemic Lectin-Glycan Interaction of Pathogenic Enteric Bacteria in the Gastrointestinal Tract. PMID:35163392
Proteome-pI 2.0: proteome isoelectric point database update. PMID:34718696
A conserved Neurite Outgrowth and Guidance motif with biomimetic potential in neuronal Cell Adhesion Molecules. PMID:34712402
How do I get the most out of my protein sequence using bioinformatics tools? PMID:34473083
Expasy, the Swiss Bioinformatics Resource Portal, as designed by its users. PMID:33849055
A Proline-Based Tectons and Supramolecular Synthons for Drug Design 2.0: A Case Study of ACEI. PMID:33114370
The Bgee suite: integrated curated expression atlas and comparative transcriptomics in animals. PMID:33037820
The Voltage-Dependent Deactivation of the KvAP Channel Involves the Breakage of Its S4 Helix. PMID:32850956
Quality Matters: Biocuration Experts on the Impact of Duplication and Other Data Quality Issues in Biological Databases. PMID:32652120
A Supramolecular Approach to Structure-Based Design with A Focus on Synthons Hierarchy in Ornithine-Derived Ligands: Review, Synthesis, Experimental and in Silico Studies. PMID:32138329
A Profile of the In Vitro Anti-Tumor Activity and In Silico ADME Predictions of Novel Benzothiazole Amide-Functionalized Imidazolium Ionic Liquids. PMID:31212762
CoCoScore: context-aware co-occurrence scoring for text mining applications using distant supervision. PMID:31199464
Proteomic and Metabolomic Characteristics of Extremophilic Fungi Under Simulated Mars Conditions. PMID:31156574
The Promoter Regions of Intellectual Disability-Associated Genes Are Uniquely Enriched in LTR Sequences of the MER41 Primate-Specific Endogenous Retrovirus: An Evolutionary Connection Between Immunity and Cognition. PMID:31031802
Evolution-guided evaluation of the inverted terminal repeats of the synthetic transposon Sleeping Beauty. PMID:30718656
Genomic data integration systematically biases interactome mapping. PMID:30332399
TISSUES 2.0: an integrative web resource on mammalian tissue expression. PMID:29617745
Computational Studies of Snake Venom Toxins. PMID:29271884
Triage by ranking to support the curation of protein interactions. PMID:29220432
Bioinformatics on a national scale: an example from Switzerland. PMID:29106442
Epithelial-to-Mesenchymal Transition Antagonizes Response to Targeted Therapies in Lung Cancer by Suppressing BIM. PMID:29051323
"Big Data" for Breast Cancer: Where to look and what you will find. PMID:28164152
World data centre for microorganisms: an information infrastructure to explore and utilize preserved microbial strains worldwide. PMID:28053166
CEBS: a comprehensive annotated database of toxicological data. PMID:27899660
neXtA5: accelerating annotation of articles via automated approaches in neXtProt. PMID:27374119
Comparative Proteomic Analysis of Mature and Immature Oocytes of the Swamp Buffalo (Bubalus bubalis). PMID:26784167 -
arrayMap: a reference resource for genomic copy number imbalances in human malignancies
PubMed citations: 19.
19 articles citing: arrayMap: a reference resource for genomic copy number imbalances in human malignancies
The ELIXIR Human Copy Number Variations Community: building bioinformatics infrastructure for research. PMID:34367618
The Progenetix oncogenomic resource in 2021. PMID:34272855
Amplifications of stemness genes and the capacity of breast tumors for metastasis. PMID:32523653
Enabling population assignment from cancer genomes with SNP2pop. PMID:32179800
ZEB1 Is a Transcription Factor That Is Prognostic and Predictive in Diffuse Gliomas. PMID:30705664
A group of long noncoding RNAs identified by data mining can predict the prognosis of lung adenocarcinoma. PMID:30290038
Integrated Molecular Meta-Analysis of 1,000 Pediatric High-Grade and Diffuse Intrinsic Pontine Glioma. PMID:28966033
GenomeCAT: a versatile tool for the analysis and integrative visualization of DNA copy number variants. PMID:28061750
CNARA: reliability assessment for genomic copy number profiles. PMID:27733115
Identification of cis- and trans-acting elements regulating calretinin expression in mesothelioma cells. PMID:26848772
Deletions of multidrug resistance gene loci in breast cancer leads to the down-regulation of its expression and predict tumor response to neoadjuvant chemotherapy. PMID:26799285
The SIB Swiss Institute of Bioinformatics' resources: focus on curated databases. PMID:26615188
Genomic instability of osteosarcoma cell lines in culture: impact on the prediction of metastasis relevant genes. PMID:25992885
arrayMap 2014: an updated cancer genome resource. PMID:25428357
Chromothripsis-like patterns are recurring but heterogeneously distributed features in a survey of 22,347 cancer genome screens. PMID:24476156
Progenetix: 12 years of oncogenomic data curation. PMID:24225322
Cancer karyotypes: survival of the fittest. PMID:23760367
Genomic profiling of oral squamous cell carcinoma by array-based comparative genomic hybridization. PMID:23457519
Specific genomic regions are differentially affected by copy number alterations across distinct cancer types, in aggregated cytogenetic data. PMID:22937079 -
arrayMap 2014: an updated cancer genome resource
PubMed citations: 10.
10 articles citing: arrayMap 2014: an updated cancer genome resource
The Progenetix oncogenomic resource in 2021. PMID:34272855
Signatures of Discriminative Copy Number Aberrations in 31 Cancer Subtypes. PMID:34054918
The Landscape of Somatic Copy Number Alterations in Head and Neck Squamous Cell Carcinoma. PMID:32226775
Comprehensive identification and characterization of somatic copy number alterations in triple‑negative breast cancer. PMID:31894314
Germline and Somatic NF1 Alterations Are Linked to Increased HER2 Expression in Breast Cancer. PMID:30104415
Customized Array Comparative Genomic Hybridization Analysis of 25 Phosphatase-encoding Genes in Colorectal Cancer Tissues. PMID:28031238
CNARA: reliability assessment for genomic copy number profiles. PMID:27733115
CTLPScanner: a web server for chromothripsis-like pattern detection. PMID:27185889
Interactive analysis of large cancer copy number studies with Copy Number Explorer. PMID:25957352
The 2015 Nucleic Acids Research Database Issue and molecular biology database collection. PMID:25593347 - http://dx.doi.org/10.1093/nar/gku1123
Tags:
Tags
More detailed information about this field from each metasource.
cancer
metasource: Fairsharing.org
version: FAIRsharing.org: arrayMap; arrayMap - Genomic Array Data for Cancer CNV Profiles; DOI: https://doi.org/10.25504/FAIRsharing.1fbc5y; Last edited: May 4, 2021, 8:16 a.m.; Last accessed: Jan 03 2022 7:06 p.m.
metasource: re3data.org
version: re3data.org: arrayMap; editing status 2021-01-20; re3data.org - Registry of Research Data Repositories. http://doi.org/10.17616/R3X78M last accessed: 2022-11-04
chromosomal aberration
metasource: Fairsharing.org
version: FAIRsharing.org: arrayMap; arrayMap - Genomic Array Data for Cancer CNV Profiles; DOI: https://doi.org/10.25504/FAIRsharing.1fbc5y; Last edited: May 4, 2021, 8:16 a.m.; Last accessed: Jan 03 2022 7:06 p.m.
metasource: re3data.org
version: re3data.org: arrayMap; editing status 2021-01-20; re3data.org - Registry of Research Data Repositories. http://doi.org/10.17616/R3X78M last accessed: 2022-11-04
dna microarray
metasource: Fairsharing.org
version: FAIRsharing.org: arrayMap; arrayMap - Genomic Array Data for Cancer CNV Profiles; DOI: https://doi.org/10.25504/FAIRsharing.1fbc5y; Last edited: May 4, 2021, 8:16 a.m.; Last accessed: Jan 03 2022 7:06 p.m.
metasource: re3data.org
version: re3data.org: arrayMap; editing status 2021-01-20; re3data.org - Registry of Research Data Repositories. http://doi.org/10.17616/R3X78M last accessed: 2022-11-04
gene expression data
metasource: Fairsharing.org
version: FAIRsharing.org: arrayMap; arrayMap - Genomic Array Data for Cancer CNV Profiles; DOI: https://doi.org/10.25504/FAIRsharing.1fbc5y; Last edited: May 4, 2021, 8:16 a.m.; Last accessed: Jan 03 2022 7:06 p.m.
human genes and diseases
metasource: Nucleic Acid Research database catalogue
version: extracted_at: 2022-11-04T11:16:25.468657
cancer gene databases
metasource: Nucleic Acid Research database catalogue
version: extracted_at: 2022-11-04T11:16:25.468657
bioinformatics
metasource: re3data.org
version: re3data.org: arrayMap; editing status 2021-01-20; re3data.org - Registry of Research Data Repositories. http://doi.org/10.17616/R3X78M last accessed: 2022-11-04
homo sapiens
metasource: re3data.org
version: re3data.org: arrayMap; editing status 2021-01-20; re3data.org - Registry of Research Data Repositories. http://doi.org/10.17616/R3X78M last accessed: 2022-11-04
systems biology
metasource: bio.tools
version: extracted_at: 2022-11-04T11:31:12.319463
genomics
metasource: bio.tools
version: extracted_at: 2022-11-04T11:31:12.319463
oncology
metasource: bio.tools
version: extracted_at: 2022-11-04T11:31:12.319463
dna structural variation
metasource: bio.tools
version: extracted_at: 2022-11-04T11:31:12.319463
Tags
More detailed information about this field from each metasource.
cancer
metasource: Fairsharing.orgversion: FAIRsharing.org: arrayMap; arrayMap - Genomic Array Data for Cancer CNV Profiles; DOI: https://doi.org/10.25504/FAIRsharing.1fbc5y; Last edited: May 4, 2021, 8:16 a.m.; Last accessed: Jan 03 2022 7:06 p.m.
metasource: re3data.org
version: re3data.org: arrayMap; editing status 2021-01-20; re3data.org - Registry of Research Data Repositories. http://doi.org/10.17616/R3X78M last accessed: 2022-11-04
chromosomal aberration
metasource: Fairsharing.orgversion: FAIRsharing.org: arrayMap; arrayMap - Genomic Array Data for Cancer CNV Profiles; DOI: https://doi.org/10.25504/FAIRsharing.1fbc5y; Last edited: May 4, 2021, 8:16 a.m.; Last accessed: Jan 03 2022 7:06 p.m.
metasource: re3data.org
version: re3data.org: arrayMap; editing status 2021-01-20; re3data.org - Registry of Research Data Repositories. http://doi.org/10.17616/R3X78M last accessed: 2022-11-04
dna microarray
metasource: Fairsharing.orgversion: FAIRsharing.org: arrayMap; arrayMap - Genomic Array Data for Cancer CNV Profiles; DOI: https://doi.org/10.25504/FAIRsharing.1fbc5y; Last edited: May 4, 2021, 8:16 a.m.; Last accessed: Jan 03 2022 7:06 p.m.
metasource: re3data.org
version: re3data.org: arrayMap; editing status 2021-01-20; re3data.org - Registry of Research Data Repositories. http://doi.org/10.17616/R3X78M last accessed: 2022-11-04
gene expression data
metasource: Fairsharing.orgversion: FAIRsharing.org: arrayMap; arrayMap - Genomic Array Data for Cancer CNV Profiles; DOI: https://doi.org/10.25504/FAIRsharing.1fbc5y; Last edited: May 4, 2021, 8:16 a.m.; Last accessed: Jan 03 2022 7:06 p.m.
human genes and diseases
metasource: Nucleic Acid Research database catalogueversion: extracted_at: 2022-11-04T11:16:25.468657
cancer gene databases
metasource: Nucleic Acid Research database catalogueversion: extracted_at: 2022-11-04T11:16:25.468657
bioinformatics
metasource: re3data.orgversion: re3data.org: arrayMap; editing status 2021-01-20; re3data.org - Registry of Research Data Repositories. http://doi.org/10.17616/R3X78M last accessed: 2022-11-04
homo sapiens
metasource: re3data.orgversion: re3data.org: arrayMap; editing status 2021-01-20; re3data.org - Registry of Research Data Repositories. http://doi.org/10.17616/R3X78M last accessed: 2022-11-04
systems biology
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:31:12.319463
genomics
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:31:12.319463
oncology
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:31:12.319463
dna structural variation
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:31:12.319463
cancer chromosomal aberration dna microarray gene expression human genes and diseases cancer-related genes bioinformatics homo sapiens systems biology genomics oncology dna structural variation
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