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Merge pull request #2094 from cBioPortal/add_study
msk_chord_2024: move files to Datahub
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Gene panels for this study can be found here: https://github.com/cBioPortal/datahub/tree/master/reference_data/gene_panels |
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cancer_study_identifier: msk_chord_2024 | ||
genetic_alteration_type: CLINICAL | ||
datatype: PATIENT_ATTRIBUTES | ||
data_filename: data_clinical_patient.txt |
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cancer_study_identifier: msk_chord_2024 | ||
genetic_alteration_type: CLINICAL | ||
datatype: SAMPLE_ATTRIBUTES | ||
data_filename: data_clinical_sample.txt |
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cancer_study_identifier: msk_chord_2024 | ||
genetic_alteration_type: COPY_NUMBER_ALTERATION | ||
datatype: DISCRETE | ||
stable_id: cna | ||
show_profile_in_analysis_tab: true | ||
profile_description: Putative copy-number from GISTIC 2.0. Values: -2 = homozygous deletion; -1 = hemizygous deletion; 0 = neutral / no change; 1 = gain; 2 = high level amplification. | ||
profile_name: Putative copy-number alterations from GISTIC | ||
data_filename: data_cna.txt |
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cancer_study_identifier: msk_chord_2024 | ||
genetic_alteration_type: COPY_NUMBER_ALTERATION | ||
datatype: SEG | ||
show_profile_in_analysis_tab: false | ||
description: Somatic CNA data (copy number ratio from tumor samples minus ratio from matched normals). | ||
profile_name: Segment data values | ||
reference_genome_id: hg19 | ||
data_filename: data_cna_hg19.seg |
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cancer_study_identifier: msk_chord_2024 | ||
genetic_alteration_type: GENE_PANEL_MATRIX | ||
datatype: GENE_PANEL_MATRIX | ||
data_filename: data_gene_panel_matrix.txt |
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cancer_study_identifier: msk_chord_2024 | ||
genetic_alteration_type: MUTATION_EXTENDED | ||
datatype: MAF | ||
stable_id: mutations | ||
show_profile_in_analysis_tab: true | ||
profile_description: Mutation data. | ||
profile_name: Mutations | ||
data_filename: data_mutations.txt |
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type_of_cancer: mixed | ||
cancer_study_identifier: msk_chord_2024 | ||
name: MSK CHORD (MSK, 2024) | ||
description: Targeted sequencing of 25040 tumors from 24950 patients and their matched normals via MSK-IMPACT, along with clinical annotations, some of which are derived from natural language processing (denoted NLP). This data is available under the <a href="https://creativecommons.org/licenses/by-nc-nd/4.0/deed.en">Creative Commons BY-NC-ND 4.0 license</a>. For commercial use, please contact [email protected] |
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cancer_study_identifier: msk_chord_2024 | ||
genetic_alteration_type: STRUCTURAL_VARIANT | ||
datatype: SV | ||
stable_id: structural_variants | ||
show_profile_in_analysis_tab: true | ||
profile_name: Structural Variants | ||
profile_description: Structural Variant Data. | ||
data_filename: data_sv.txt |