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Data from 2021 Signatures Publication

Genomic CNVs from publication...
This search page uses the subset of Progenetix data - including TCGA samples - used in the Signatures of Discriminative Copy Number Aberrations in 31 Cancer Subtypes publication.
For access restriction imposed by PCAWG the data cannot not include the samples from this consortium which have been used in our publication.
Downloads and Source Links
  • All Progenetix(arrayMap)samples and segmentations used in the study
  • All TCGA samples and segmentations used in the study
  • IDs of all Progenetix(arrayMap) samples used in the study
  • IDs of all TCGA files used in the study
  • IDs of all PCAWG files used in the study
  • Metadata of Progenetix(arrayMap) samples
  • Metadata of TCGA samples
CNV Frequency Plot
Download SVG | Go to pgx:cohort-gao2021signatures | Download CNV Frequencies
Search Samples
© 2000 - 2023 Progenetix Cancer Genomics Information Resource by the Computational Oncogenomics Group at the University of Zurich and the Swiss Institute of Bioinformatics SIB is licensed under CC BY 4.0
No responsibility is taken for the correctness of the data presented nor the results achieved with the Progenetix tools.