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Update Study ID #1762

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Feb 2, 2023
Merged

Update Study ID #1762

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3 changes: 0 additions & 3 deletions public/nst_nfosi_2022/data_clinical_sample.txt
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8 changes: 0 additions & 8 deletions public/nst_nfosi_2022/meta_study.txt
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0 public/nst_nfosi_2022/LICENSE → public/nst_nfosi_ntap/LICENSE
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4 changes: 2 additions & 2 deletions ...c/nst_nfosi_2022/case_lists/cases_all.txt → ...c/nst_nfosi_ntap/case_lists/cases_all.txt
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cancer_study_identifier: nst_nfosi_2022
stable_id: nst_nfosi_2022_all
cancer_study_identifier: nst_nfosi_ntap
stable_id: nst_nfosi_ntap_all
case_list_name: All samples
case_list_description: All samples (19 samples)
case_list_category: all_cases_in_study
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4 changes: 2 additions & 2 deletions ...nfosi_2022/case_lists/cases_sequenced.txt → ...nfosi_ntap/case_lists/cases_sequenced.txt
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cancer_study_identifier: nst_nfosi_2022
stable_id: nst_nfosi_2022_sequenced
cancer_study_identifier: nst_nfosi_ntap
stable_id: nst_nfosi_ntap_sequenced
case_list_name: Samples with mutation data
case_list_description: Samples with mutation data (19 samples)
case_list_category: all_cases_with_mutation_data
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0 .../nst_nfosi_2022/data_clinical_patient.txt → .../nst_nfosi_ntap/data_clinical_patient.txt
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3 changes: 3 additions & 0 deletions public/nst_nfosi_ntap/data_clinical_sample.txt
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0 public/nst_nfosi_2022/data_mutations.txt → public/nst_nfosi_ntap/data_mutations.txt
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2 changes: 1 addition & 1 deletion .../nst_nfosi_2022/meta_clinical_patient.txt → .../nst_nfosi_ntap/meta_clinical_patient.txt
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cancer_study_identifier: nst_nfosi_2022
cancer_study_identifier: nst_nfosi_ntap
genetic_alteration_type: CLINICAL
datatype: PATIENT_ATTRIBUTES
data_filename: data_clinical_patient.txt
2 changes: 1 addition & 1 deletion ...c/nst_nfosi_2022/meta_clinical_sample.txt → ...c/nst_nfosi_ntap/meta_clinical_sample.txt
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cancer_study_identifier: nst_nfosi_2022
cancer_study_identifier: nst_nfosi_ntap
genetic_alteration_type: CLINICAL
datatype: SAMPLE_ATTRIBUTES
data_filename: data_clinical_sample.txt
2 changes: 1 addition & 1 deletion public/nst_nfosi_2022/meta_mutations.txt → public/nst_nfosi_ntap/meta_mutations.txt
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cancer_study_identifier: nst_nfosi_2022
cancer_study_identifier: nst_nfosi_ntap
genetic_alteration_type: MUTATION_EXTENDED
datatype: MAF
stable_id: mutations
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8 changes: 8 additions & 0 deletions public/nst_nfosi_ntap/meta_study.txt
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cancer_study_identifier: nst_nfosi_ntap
type_of_cancer: nst
name: Nerve Sheath Tumors (John Hopkins, Sci Data 2020)
description: Whole-exome sequencing of 18 patients with matched Nerve Sheath tumor-normal samples. The data is contributed by John Hopkins University researchers funded by the Neurofibromatosis Therapeutic Acceleration Program (NTAP). The reprocessing of the raw data is managed by the NF Open Science Initiative (<a href="https://nf.synapse.org/">NF Data Portal</a>).
citation: Pollard et al. Sci Data 2020
pmid: 32561749
reference_genome: hg38
groups: PUBLIC