-
Highlighted samples from the BCH CRDC
Study
EGAS00001004436
-
Integrated molecular analysis of adult T-cell leukemia/lymphoma
Study
EGAS00001001296
-
Signatures of mismatch repair deficiency in cancer genomes
Study
EGAS00001000182
-
Australia_and_New_Guinea_haplotype_phasing_
Study
EGAS00001001853
-
Keratinocyte_CRISPR_screens
Study
EGAS00001002714
-
WES of melanoma tumors treated with combined immune checkpoint blockade
Study
EGAS00001003857
-
2015_AML_ETO
Study
EGAS00001002897
-
2015_AML_ETO_WGS_additional
Study
EGAS00001002898
-
Whole exome sequencing of 76 individuals with familial atrial fibrillation
Study
EGAS00001003207
-
DCM-cases
Dataset
EGAD00001003390
-
DCM-controls
Dataset
EGAD00001003391
-
Whole Exome Sequencing of 60 tumor/normal matched liver Cancers (HCC)
Dataset
EGAD00001004180
-
Paediatric_CNS_tumour_autopsy_DNA_WES
Study
EGAS00001005642
-
Paired healthy & tumor organoid Biobank _B16PON
Study
EGAS00001005937
-
Primary_DIPG_expression_profiles
Study
EGAS00001007181
-
RSV infection of primary bronchial epithelial cells in asthma
Study
EGAS00001007450
-
FASTQ files
Dataset
EGAD00001006485
-
WGS and WES of Advance Prostate Cancer
Dataset
EGAD00001006487
-
High-throughput sequencing data of immunoglobulin gene rearrangements in acute lymphoblastic leukaemia - summary .fastq and .bcl files
Dataset
EGAD00001001983
-
Expression quantitative trait locus mapping in human pancreatic islets of Langerhans
Dataset
EGAD00001001601
-
Myeloproliferative Disease Whole Genomes
Dataset
EGAD00001000385
-
Myelodysplastic syndrome whole genomes
Dataset
EGAD00001000386
-
Chondrosarcoma Validation Study
Dataset
EGAD00001000392
-
Identification of low frequency variants associated with ulcerative colitis using whole-genome sequencing
Dataset
EGAD00001000409
-
33 Paired (Normal-Tumor1-Tumor2) MM whole-exome data
Dataset
EGAD00001002165