-
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
-
Whole_genome_sequencing_of_in_vitro_colonies
Study
EGAS00001003112
-
Single cell RNA-sequencing of GSCs and GBM tumours
Study
EGAS00001004656
-
RNA-sequencing of Non-muscle Invasive Bladder cancer (NMIBC)
Study
EGAS00001004358
-
ICGC PedBrain DNA methylation sequencing
Study
EGAS00001000561
-
ESGI___Whole_Genome_Sequencing_of_samples_from_the_INGI_Val_Borbera_genetic_isolate__X10_
Study
EGAS00001001123
-
Phylogenetic evolution of metastatic melanoma.
Study
EGAS00001003582
-
Extramammary Paget Disease
Study
EGAS00001004746
-
AML clonal phylogeny
Study
EGAS00001001779
-
ChIP Seq data of multiple myeloma and plasma cell leukaemia cell lines
Study
EGAS00001002414
-
DNA methylation in bronchial biopsies of asthmatics, asthma in remission and healthy subjects
Study
EGAS00001003739
-
Pancreatic Cancer Sequencing Initiative OICR
Study
EGAS00001000395
-
Congenital_Heart_Disease___Pilot
Study
EGAS00001000425
-
circulating-tumor DNA sequencing of healthy samples
Study
EGAS00001003989
-
Whole genome bisulfite sequencing on 10 multiple myeloma cases
Study
EGAS00001004346
-
Exploring_the_landscape_of_somatic_mutations_in_normal_tissue___GI___LYNCH___WGS
Study
EGAS00001003882
-
Exploring_the_landscape_of_somatic_mutations_in_normal_tissue___GI___MAP___WGS
Study
EGAS00001004122
-
To determine the genomic profile of Triple Negative Breast Cancer patient-derived xenografts (PDX cohort)
Study
EGAS00001005995
-
Res1_HT29_exp2_MC_03_03_22
Study
EGAS00001006093
-
Res1_H23_exp1_MC_04_03_22
Study
EGAS00001006091