-
HipSci HumanHT 12v4 Expression BeadChip analysis-Rare_BBS
Study
EGAS00001001276
-
Whole exome sequencing data for patients with Bosma arhinia microphthalmia syndrome (BAMS).
Study
EGAS00001002193
-
IBD_Whole_Genome_Sequencing
Study
EGAS00001002238
-
We evaluate the PGD/PGS including 129 couples with NGS test and 266 couples with SNP-array test for the detection of embryonic chromosomal abnormalities.
Study
EGAS00001000981
-
HipSci whole exome sequencing for embryonic stem cell control lines
Study
EGAS00001001726
-
HipSci expression microarray for embryonic stem cell control lines
Study
EGAS00001001729
-
HipSci HumanHT 12v4 Expression BeadChip analysis - monogenic diabetes
Study
EGAS00001001277
-
The_impact_of_the_human_leukaemia_virus_HTLV_1_on_host_gene_expression
Study
EGAS00001002259
-
PacBio Rare Disease Study
Study
EGAS00001008170
-
GILD_ExomeSeq_PTNHL
Study
EGAS00001001613
-
RNA_expression_profiling_of_melanoma_patient_derived_xenograft
Study
EGAS00001001537
-
MDSMPN_Rearrangement_Screen
Study
EGAS00001000034
-
HG Transcriptome sequencing in the INTERVAL cohort
Study
EGAS00001003346
-
Study_to_investigate_the_prevalence__of_leukaemic_mutations_in_whole_blood_DNA_in_a_cohort_of_blood_donors
Study
EGAS00001000814
-
Gastric_and_Esophageal_tumour_rearrangement_screen
Study
EGAS00001000037
-
Investigation of the genetic basis of the rare syndrome Post-Transfusion Purpura (PTP)
Study
EGAS00001000053
-
Roma Sequencing Study
Study
EGAS00001004287
-
Genetic characterization patients affected by Cancer of Unknown Primary
Study
EGAS00001006621
-
Splenic_Marginal_Zone_Lymphoma_with_villous_lymphocytes_exome_sequencing
Study
EGAS00001000139
-
Cancer_Genome_Project_Exome_Sequencing
Study
EGAS00001000301
-
Matched_Ovarian_Cancer_Sequencing
Study
EGAS00001000155
-
Chondrosarcoma_Validation_Study
Study
EGAS00001000181
-
Acute_Myeloid_Leukemia_Sequencing
Study
EGAS00001000209
-
RNAseq of Follicular Lymphoma
Study
EGAS00001002980
-
SLC9A3R1 variant associated with age-related hearing loss
Study
EGAS00001003072
-
FGFP and TR-MDD shotgun sequencing samples (N=157)
Study
EGAS00001003298
-
The analysis of mtDNA variability of the modern Polish population
Study
EGAS00001003309
-
Longitudinal therapy monitoring of ALK-positive non-small cell lung cancer (copy number, cell-free DNA)
Study
EGAS00001004276
-
ATAC_SEQ_MAIN___PHASE_1
Study
EGAS00001000947
-
RNA sequencing data from visceral and abdominal subcutaneous adipose tissue from morbidly obese women with normal glucose tolerance or type 2 diabetes
Study
EGAS00001001872
-
HipSci HumanHT 12 Expression BeadChip analysis - Hereditary Cerebellar Ataxias
Study
EGAS00001002020
-
Analysis of tumor periphery and center-specific mutations in renal cell carcinoma
Study
EGAS00001001784
-
Mutation_analysis_in_human_iPS_cells_
Study
EGAS00001000359
-
QSEA – modelling of genome-wide DNA methylation from sequencing enrichment experiments
Study
EGAS00001001822
-
Detecting and tracking circulating tumour DNA copy number profiles during first line chemotherapy in oesophagogastric adenocarcinoma
Study
EGAS00001003695
-
Genomewide detection of cytosine methylation by single molecule real-time sequencing
Study
EGAS00001004642
-
Foetal_phylogeny_8pcw___WGS_of_LCM_tissues
Study
EGAS00001004674
-
Immunological hallmarks for clinical response to BCG in bladder cancer
Study
EGAS00001004764
-
Summary statistics of meta-analysis using two genome-wide association study of inflammatory bowel disease in Koreans.
Study
EGAS00001005026
-
To reveal the spectrum of gene mutations in grade II/III gliomas, whole exome sequencing of 52 samples including 4 multi-regional and 10 multi-time points sampling cases and 291 SNP-array were performed.
Study
EGAS00001001044
-
HipSci HumanHT 12 Expression BeadChip analysis - Primary immune deficiency
Study
EGAS00001002027
-
HipSci HumanHT 12 Expression BeadChip analysis - Bleeding and Platelet disorders
Study
EGAS00001002028
-
Comprehensive investigation of genome architecture of papillary thyroid cancer with whole-exon sequencing in the Chinese population.
Study
EGAS00001002402
-
Spontaneous mutations in the single TTN gene represent high tumor mutation burden
Study
EGAS00001004009
-
Y chromosome variability in Polish population
Study
EGAS00001004111
-
Prospective high-throughput genome profiling in advanced cancers:
Study
EGAS00001004554
-
Whole-genome sequencing identifies ADGRG6 enhancer mutations and FRS2 duplications as angiogenesis-related drivers in bladder cancer
Study
EGAS00001003388
-
Targeted sequencing DDR genes in cancer stem cells
Study
EGAS00001004892
-
46 patients primary malignant glioma cohort in Chinese population
Study
EGAS00001005583
-
Saliva microbiota in Finnish children
Study
EGAS00001003039
-
Gut metagenome/FINRISK 2002 (Salosensaari et al. Nature Comms 2021)
Study
EGAS00001005020
-
MM samples for epigenomic translocation of H3K4me3 broad domains following super-enhancer hijacking
Study
EGAS00001005684
-
The Landscape of Genetic Alterations in Hepatocellular Carcinoma, 88 matched HCC tumour/normal pairs WGS belongs to ICGC LICA-CN project
Study
EGAS00001002218
-
DNA sequencing for human normal endometrial glands
Study
EGAS00001005822
-
Molecular characterization of hepatocellular carcinoma in patients with non-alcoholic steatohepatitis
Study
EGAS00001005222
-
TP53 variant detection analysis in high grade serous epithelial ovarian cancer
Study
EGAS00001004361
-
Epigenetic analyses of methylation and nucleosome occupancy in cell-free DNA (cfNOMe)
Study
EGAS00001004370
-
Molecular profile of IMFT for the identification of potential druggable targets and biomarkers predicting crizotinib response.
Study
EGAS00001005419
-
A GWAS meta-analysis on severe acne on a European population of 26,722 individuals
Study
EGAS00001003278
-
Whole genome sequencing of tumour and matched normal from patients with family history of breast cancer
Study
EGAS00001003305
-
RNAseq Iron-Treated iPSC-derived Microglia
Study
EGAS00001006112
-
Somatic L1 retrotranspositions in normal human cells
Study
EGAS00001006213
-
Genomic abnormalities of TP53 define distinct risk groups of paediatric B-cell non-Hodgkin lymphoma
Study
EGAS00001005617
-
Multiomics Characterization of Low-grade Serous Ovarian Carcinoma
Study
EGAS00001004724
-
Discriminating Th17.1 cell driven sarcoidosis-like inflammation from relapse after anti-BCMA CAR T cells in multiple myeloma
Study
EGAS00001006133
-
DNA and RNA sequencing data from Ovarian Carcinosarcoma patients from the Glasgow Cohort.
Study
EGAS00001006605
-
Study the genetic susceptibility of esophagus squamous cell carcinomas (ESCC) in high-risk area Henan Chinese
Study
EGAS00001003423
-
Gene regulation of human stimulated and cultured CD4+ Treg cells
Study
EGAS00001003515
-
Single-cell transcriptome landscape of developing fetal gonads defines somatic cell lineage specification in humans
Study
EGAS00001006568
-
Exome and Whole-Genome Sequencing of Central African Hunter-Gatherers and Agriculturalists
Study
EGAS00001003722
-
SPECIAL: Dissecting the melanoma ecosystem one cell at the time during immunotherapy
Study
EGAS00001006488
-
Characterization of a novel MEF2D-BCL9 fusion positive acute lymphoblastic leukemia cell line WXS derived
Study
EGAS00001006801
-
A single-cell transcriptional gradient in human cutaneous memory T cells restricts Th17/Tc17 identity
Study
EGAS00001006716
-
Population_based_analysis_of_POT1_variants_in_a_cutaneous_melanoma_case_control_cohort
Study
EGAS00001006870
-
Vitamin C boosts DNA demethylation in TET2 germline mutation carriers
Study
EGAS00001006916
-
Preeclampsia InterPregGen Consortium: Whole Genome Sequencing of 100 unrelated Uzbeks (DNA samples from the Institute of Immunology, Uzbek Academy of Sciences, Tashkent, Uzbekistan; Republic Specialized Scientific Practical Medical Centre of Obstetrics and Gynecology, Tashkent, Uzbekistan)
Dataset
EGAD00001005466
-
Strand-seq of hematopoietic stem and progenitor cells along human aging
Dataset
EGAD00001009402
-
WTS data of patients diagnosed with angiosarcoma
Dataset
EGAD00001005367
-
Heterogeneous metabolic signatures are linked to cancer cell differentiation in colorectal cancer
Dataset
EGAD00001005524
-
Pediatric Papillary Thyroid Carcinoma RNA-Seq
Dataset
EGAD00001007499
-
Berlin Neuroblastoma Patient Genomic Data from Targeted Sequencing for Detection of TERT rearrangement breakpoints to monitor neuroblastoma
Dataset
EGAD00001011088
-
Evolutionary trajectories and clonal migration underlying tumor progression and lymph node metastasis in resectable lung cancer
Dataset
EGAD00001007587
-
Inherited MUTYH mutations cause elevated somatic mutation rates and distinctive mutational signatures in normal human cells
Dataset
EGAD00001007997
-
Transcriptome and epigenome characterization of BMP signaling effects on H3.3K27M DIPG
Dataset
EGAD00001007768
-
Pre-neoplastic somatic mutations including MYD88L265P in lymphoplasmacytic lymphoma
Dataset
EGAD00001008196
-
MutWP5: CRUK Mutographs of Cancer: Lung: PD37920 (Targeted) (2021-02-02)
Dataset
EGAD00001006929
-
High hyperdiploid ALL single cell whole genome sequencing
Dataset
EGAD00001008988
-
Bone marrow microenvironment of 6 newly diagnosed myeloma patients using 10X Genomics scRNA- and TCR-sequencing
Dataset
EGAD00001009270
-
Shallow whole genome sequencing and targeted capture sequencing data of PCNSL and PTL primary and relapse pairs
Dataset
EGAD00001008387
-
Liver CD14+CD8+ T cells scRNAseq dataset
Dataset
EGAD00001009831
-
GEX CITE-Seq performance dataset
Dataset
EGAD00001008418
-
ADT/SPEX CITE-Seq performance dataset
Dataset
EGAD00001008419
-
Dataset for soft_tissue_tumor-WHOLE_GENOME
Dataset
EGAD00001008900
-
UCSF WCDT WGS/WGBS mCRPC
Dataset
EGAD00001009505
-
PPGL WES dataset
Dataset
EGAD00001008579
-
Immune profiling reveals enrichment of distinct immune signatures in oral epithelial dysplasia
Dataset
EGAD00001007970
-
Human Skeletal Muscles Transcriptome
Dataset
EGAD00001008657
-
The transcriptomic response of skeletal muscle in life-long high-level trained and untrained men and women after acute exercise
Dataset
EGAD00001008663
-
Lung cancer and non-cancerous plasma cfDNA samples
Dataset
EGAD00001008666
-
Pooled Single-Cell RNA-Seq of iPSC-Derived Neural Stem Cells from ADHD and Control Individuals
Dataset
EGAD00001015644