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UROMOL 2020 - RNA-seq data for validation
Study
EGAS00001005050
-
LLNEXT Pilot MGS sequencing
Dataset
EGAD00001011293
-
Nasal brushes analysis
Study
EGAS00001006657
-
ORIENT study
Dataset
EGAD00001009687
-
Metadata file
Dataset
EGAD00001008792
-
WXS files for MATCH paper
Dataset
EGAD00001015484
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RRBS melanoma biopsies
Dataset
EGAD00001009060
-
RNASeq files for Stewart-MATCH
Dataset
EGAD00001015475
-
RPPA analysis + clinical data
Dataset
EGAD00001008507
-
DATA FILES FOR SJLGG
Dataset
EGAD00001000695
-
Seminoma exome sequencing
Dataset
EGAD00001001002
-
LGG Epilepsy Cohort WGS
Dataset
EGAD00001001664
-
LGG Epilepsy Cohort WXS
Dataset
EGAD00001001665
-
Osteosarcoma exome sequencing dataset
Dataset
EGAD00001002145
-
Characterization of HCV-specific CD4 T cells during DAA-Therapy
Dataset
EGAD00001005432
-
Melanoma multi site metastases
Dataset
EGAD00001005483
-
KRAS Mutations in Multiple Myeloma
Dataset
EGAD00001005743
-
Proteome data
Dataset
EGAD00001006737
-
Global Anaplastic Thyroid Cancer Initiative
Dataset
EGAD00001003236
-
Plasma DNA motif analysis
Study
EGAS00001003409
-
Data Access Committee for the DNA sequencing data included in the study "A generalizable machine learning framework for classifying DNA repair defects using ctDNA exomes”
Dac
EGAC00001003111
-
African Partnership for Chronic Disease Research (APCDR) DAC
Dac
EGAC00001000237
-
Data Access Committee of DKFZ-Epigenomics
Dac
EGAC00001000279
-
DAC for the Study EGAS00001006374:
Pathogenic variants damage cell composition and single cell transcription in cardiomyopathies.
snRNAseq of 79 (61 CM patients + 18 controls).
Dac
EGAC00001002804
-
EGAD00000000010
Dataset
EGAD00000000010
-
EGAD00000000013
Dataset
EGAD00000000013
-
EGAD00000000049
Dataset
EGAD00000000049
-
EGAD00010000636
Dataset
EGAD00010000636
-
EGAD00010000638
Dataset
EGAD00010000638
-
EGAD00010000640
Dataset
EGAD00010000640
-
EGAD00010000674
Dataset
EGAD00010000674
-
EGAD00010000676
Dataset
EGAD00010000676
-
EGAD00010000294
Dataset
EGAD00010000294
-
EGAD00010000236
Dataset
EGAD00010000236
-
EGAD00010000286
Dataset
EGAD00010000286
-
EGAD00010000290
Dataset
EGAD00010000290
-
EGAD00010000298
Dataset
EGAD00010000298
-
EGAD00010000450
Dataset
EGAD00010000450
-
EGAD00010000486
Dataset
EGAD00010000486
-
EGAD00010000496
Dataset
EGAD00010000496
-
"SNV detection from formalin fixed paraffin embedded (FFPE) samples"
Dataset
EGAD00001000033
-
"Usage of small amounts of DNA for Illumina sequencing"
Dataset
EGAD00001000034
-
Cell Line Sub Clone Rearrangement Screen
Dataset
EGAD00001000064
-
Non Tumour Renal Cell Line Sequencing
Dataset
EGAD00001000091
-
Identifying Novel Fusion Genes in Myeloma
Dataset
EGAD00001000112
-
AML targeted resequencing study
Dataset
EGAD00001000253
-
Plasma DNA tissue mapping by genome-wide methylation sequencing for noninvasive prenatal, cancer, and transplantation assessments
Dataset
EGAD00001001602
-
450K_DKFZ_CLL_NB
Dataset
EGAD00010000871
-
ICGC_450k
Dataset
EGAD00010001323
-
Second generation noninvasive fetal genome analysis reveals de novo mutations, single-base parental inheritance, and preferred DNA ends
Dataset
EGAD00001003778