-
Spontaneously differentiatiated iPSCs to EBs
Study
EGAS50000001094
-
WES - Characterization of a Breast Patient-derived Tumor Organoid biobank from an underserved population of patients.
Study
EGAS50000000684
-
RNA-Seq of primary pediatric kidney tumor controls for the soft tissue sarcoma tumoroid biobank
Dataset
EGAD00001008709
-
Data access committee for "Detection of brain cancer using genome-wide cell-free DNA fragmentomes"
Dac
EGAC50000000605
-
Human exome sequencing data (n=2) from the publication "Germline variants in UHRF1 are associated with multi-locus imprinting disturbance in humans and mice"
Dataset
EGAD50000001684
-
scWGS profile, paediatric acute lymphoblastic leukemia ALL40
Dataset
EGAD50000001774
-
Fluctuating DNA methylation tracks cancer evolution at clinical scale
Study
EGAS50000001192
-
BipEx_Owen_Cardiff
Dac
EGAC50000000139
-
Dac for "ARHGAP11A Maintains Cortical Progenitor Identity Through RHOA–ROCK Signalling During Human Brain Development" with Julia.ladewig@zi-mannheim.de, Department of Translational Brain Research. Moritz Mall, m.mall@dkfz-heidelberg.de, German Cancer Research Center (DKFZ). Yannick Hass, yannick.hass@zi-mannheim.de, Department of Translational Brain Research. Anne Hoffrichter, anne.hoffrichter@zi-mannheim.de, Department of Translational Brain Research, Central Institute of Mental Health
Dac
EGAC00001003603
-
Single-nucleus RNA-sequencing of normal adrenal cortex and adrenocortical tumors
Study
EGAS50000000585
-
cfDNA sWGS BAM — Metastatic colorectal cancer
Dataset
EGAD50000001879
-
DAC Magna Græcia University of Catanzaro - WGS of Healthy and PSP Donors
Dac
EGAC50000000709
-
Nanopore sequencing of FSHD, BAMS and healthy control fibroblast cell lines
Study
EGAS50000001065
-
Ultra-long whole-genome and Cas9-targeted nanopore sequencing of fibroblasts: FSHD, BAMS, healthy controls
Dataset
EGAD50000001551
-
RIP-seq of SF3B4 binding RNA fragments
Study
EGAS50000001129
-
Pediatric B-cell precursor acute lymphoblastic leukemia RNA sequencing
Study
EGAS50000000763
-
WES_dataset2
Dataset
EGAD50000001621
-
WES Analysis of CRC and UC samples from a cohort of Lynch Syndrome carriers
Dataset
EGAD50000001915
-
miRNA
Dataset
EGAD50000002025
-
HOVON152 Trial shallow Whole Genome Sequencing
Dataset
EGAD50000002094
-
RNA isoform diversity, splicing variants, and switching in single cells of the Alzheimer’s disease brain
Dataset
EGAD50000002124
-
DAC for study CMMRD–associated high-grade glioma
Dac
EGAC50000000855
-
DDD-Africa Exome Sequencing
Dataset
EGAD00001015728
-
BipEx_Adolfsson_Umea
Dac
EGAC50000000133
-
Dataset for desmoplastic small round cell tumor - WGS
Dataset
EGAD50000000911
-
Integrated Multiomics Uncovers Distinct Macrophage Alterations in Human Metabolic dysfunction-Associated Steatohepatitis Progression
Dataset
EGAD50000001129
-
WHOLE GENOME SEQUENCING OF CLEAR CELL RENAL CELL CARCINOMA IN VHL PATIENT
Study
EGAS50000000295
-
RNA-Sequencing of whole blood collected from RNU4ATAC/RNU6ATC patients and controls
Dataset
EGAD50000002242
-
Bulk RNASeq of metastatic colorectal cancer organoids with ATOH1 knockout
Dataset
EGAD50000002060
-
Enzymatic Methyl-Seq Rectal Mucus
Study
EGAS50000001314
-
Sequence variation of rs774984872G>T
Dataset
EGAD50000002135
-
WGS for 21 samples
Dataset
EGAD50000001790
-
Sorted WGS for three samples
Dataset
EGAD50000001792
-
16S rRNA Rectal Mucus
Study
EGAS50000001262
-
WES dataset
Dataset
EGAD50000001164
-
Whole-genome sequencing of endometrial cancer plasma circulating DNA
Dataset
EGAD50000002263
-
Genentech Small Cell Lung Cancer (SCLC) Screen
Study
EGAS00001000334
-
NGS_based_viability_screening_using_haploid_cell_line
Study
EGAS00001001095
-
G-SAM: Transcriptional Evolution of Glioblastomas Treated With Standard of Care
Study
EGAS00001005436
-
A GWAS study with the AlpeDPD study cohort
Study
EGAS00001007855
-
TraIT Cell Line use case
Study
EGAS00001001476
-
Gene expression by RNAseq in bronchial biopsies of asthmatics, asthma in remission and healthy subjects
Study
EGAS00001003735
-
Second generation noninvasive fetal genome analysis reveals de novo mutations, single-base parental inheritance, and preferred DNA ends
Study
EGAS00001001882
-
Matched_Pair_Cancer_Cell_line_Whole_Genomes
Study
EGAS00001000160
-
MPN_TGS2_Follow_up___PT1_Vori_other
Study
EGAS00001000765