-
Whole blood RNAseq from a large ALS case-control study at Univ of Michigan
Dataset
EGAD50000001488
-
ChIP-seq data in MSC_Pat and EWIma1 (FLI1 & H3K27ac)
Study
EGAS50000001172
-
RNA-seq data in hMPC, MSC_Pat and EWIma
Study
EGAS50000001173
-
Olink Explore Protein Expression
Dataset
EGAD50000001327
-
WES analysis of tumor samples from ER+ breast cancer patients treated with CDK4/6 inhibitor
Dataset
EGAD50000000622
-
A distinct monocyte cellular state links systemic immune dysregulation to pulmonary impairment in long COVID
Study
EGAS50000001215
-
ovarian cancer sample RNA-seq
Dataset
EGAD50000000613
-
SCANDARE TNBC transcriptomics data
Dataset
EGAD50000001416
-
RNA004 DRS METTL5 variant
Study
EGAS50000001321
-
Molecular profiles in early onset prostate cancer
Study
EGAS50000001467
-
cfMeDIP-seq for 18 patients with pleural mesothelioma
Dataset
EGAD50000002126
-
Oropharynx cancers sequencing study (RNA-seq from FFPE)
Study
EGAS50000000893
-
Benchmarking V(D)J Repertoire Reconstruction: Bulk RNA-Seq vs PCR-Based RepSeq Validated by SMRT Sequencing
Study
EGAS50000001541
-
Transcriptomic subgroups in soft tissue tumors correlate with morphologic subtype, genomic features, and outcome
Study
EGAS50000001472
-
Bulk RNAseq FASTQ files of WNT7B reporter PDAC organoids (P28 and P40) sorted by mNeonGreen high and low
Dataset
EGAD50000002218
-
Single cell RNAseq FASTQ files of three PDAC organoid lines (P28, P40, P47) using SORT-seq
Dataset
EGAD50000002220
-
Survival and safety of laser interstitial thermal therapy and adjuvant pembrolizumab in recurrent high-grade astrocytoma: a Phase 1/randomized Phase 2b trial
Dataset
EGAD50000001639
-
A single-cell atlas of the early COPD lung
Study
EGAS50000000720
-
Transcriptomic insights into IPMN-associated PDAC progression
Study
EGAS50000001540
-
scMultiome (snRNA + snATAC) data of 26 regionally sampled GBM tissue from 6 patients
Dataset
EGAD50000001838
-
Five Mantle Cell Lymphoma Patients Before and After Failure of Standard Chemotherapy
Dataset
EGAD50000001213
-
Viral evasion Strategy for Generating Hypoimmunogenic hiPSC Lines
Study
EGAS50000001618
-
Transcriptomic profiling of myeloid cells from secondary lymphoid organs (lymph nodes and tonsils) from lymphoma patients and controls.
Study
EGAS50000001135
-
Study of the role of aneuploidy in cB-ALL
Study
EGAS50000001613
-
HipSci HumanHT 12v4 Expression BeadChip analysis-Rare_BBS
Study
EGAS00001001276
-
Inherited damaging mutations in immune-related genes favour the development of genetically heterogeneous synchronous colorectal cancer.
Study
EGAS00001001461
-
Breast_Cancer_Exome_Resequencing
Study
EGAS00001000207
-
Reproducibility of variant calls in replicate next generation sequencing experiments
Study
EGAS00001000826
-
Exome_sequencing_of_Congenital_Heart_Disease_families_from_the_Competence_Network_Berlin
Study
EGAS00001000368
-
RNAseq_of_ribosomal_footprints
Study
EGAS00001001591
-
Meta-analysis of Genome-Wide-Association Sudies for plasma Factor XI
Study
EGAS00001002123
-
HipSci HumanExome BeadChip analysis - Usher syndrome and congenital eye defects
Study
EGAS00001002008
-
HipSci HumanExome BeadChip analysis - Bleeding and Platelet disorders
Study
EGAS00001002013
-
HipSci expression microarray for embryonic stem cell control lines
Study
EGAS00001001729
-
Integrated Molecular Profilting in Advanced Cancers Trial
Study
EGAS00001001897
-
HipSci___Whole_Exome_sequencing___Usher syndrome and congenital eye defects
Study
EGAS00001001985
-
HipSci HumanHT 12 Expression BeadChip analysis - Hereditary Spastic Paraplegia
Study
EGAS00001002021
-
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 HumanHT 12v4 Expression BeadChip analysis - monogenic diabetes
Study
EGAS00001001277
-
GILD_ExomeSeq_PTNHL
Study
EGAS00001001613
-
RNA_expression_profiling_of_melanoma_patient_derived_xenograft
Study
EGAS00001001537
-
HipSci whole exome sequencing for embryonic stem cell control lines
Study
EGAS00001001726
-
MDSMPN_Rearrangement_Screen
Study
EGAS00001000034
-
Whole_Genome_sequencing_of_individuals_from_Val_Borbera__Italy
Study
EGAS00001000458
-
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
-
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
-
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
-
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
-
UAMS Smoldering Myeloma Timeline Cohort
Dataset
EGAD00001005056
-
WTS data of patients diagnosed with angiosarcoma
Dataset
EGAD00001005367
-
MutWP5: CRUK Mutographs of Cancer: Lung: PD37920 (Targeted) (2021-02-02)
Dataset
EGAD00001006929
-
Transcriptome and epigenome characterization of BMP signaling effects on H3.3K27M DIPG
Dataset
EGAD00001007768
-
Single cell transcriptomes of of primary tumors and normal endometrial derived organoids treated with DBZ
Dataset
EGAD00001006280
-
Cell line data (RNAseq, ATACseq, ChIPseq)
Dataset
EGAD00001005493
-
Heterogeneous metabolic signatures are linked to cancer cell differentiation in colorectal cancer
Dataset
EGAD00001005524
-
Computational approach to discriminate human and mouse sequences in patient-derived tumour xenografts
Dataset
EGAD00001003800
-
Single-cell RNA sequencing on 11,138 single T cells from 12 colon and rectal cancer (CRC) patients
Dataset
EGAD00001003910
-
Genomic alterations in MM - BAM
Dataset
EGAD00001004117
-
Gene expression by RNAseq in bronchial biopsies of asthmatics, asthma in remission and healthy subjects
Dataset
EGAD00001005112
-
MutWP5: CRUK Mutographs of Cancer: Lung: PD38234 (Targeted) (2020-01-29)
Dataset
EGAD00001005925
-
ExomeSeq-EGAS00001001306
Dataset
EGAD00001001464
-
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
-
Whole exome sequencing data of tumor/normal pairs for the study "TGF-β attenuates tumour response to PD-L1 blockade by contributing to exclusion of T cells"
Dataset
EGAD00001004218
-
Pilot experiment on functional genomics in osteoarthritis_RNA
Dataset
EGAD00001001331
-
Whole Genome Sequencing of Liver Cancers
Dataset
EGAD00001003281
-
The Causes of Clonal Blood Cell Disorders Study - SCOR (2018-04-19)
Dataset
EGAD00001004086
-
Genomic characterization of germ-cell tumors in childhood
Study
EGAS50000000619
-
WES of sorted B lineage cells from patients with plasma cell neoplasms
Study
EGAS50000001498
-
Roma Sequencing Study
Study
EGAS00001004287
-
Summary statistics of meta-analysis using two genome-wide association study of inflammatory bowel disease in Koreans.
Study
EGAS00001005026
-
Whole exome sequencing data for patients with Bosma arhinia microphthalmia syndrome (BAMS).
Study
EGAS00001002193
-
Novel manifestations of immune dysregulation and granule defects in gray platelet syndrome
Study
EGAS00001004216
-
Single-cell transcriptome landscape of developing fetal gonads defines somatic cell lineage specification in humans
Study
EGAS00001006568
-
Characterization of a novel MEF2D-BCL9 fusion positive acute lymphoblastic leukemia cell line WXS derived
Study
EGAS00001006801
-
Long-read sequencing for cell-free DNA analysis (human)
Study
EGAS00001006328
-
RNAseq of Follicular Lymphoma
Study
EGAS00001002980
-
FGFP and TR-MDD shotgun sequencing samples (N=157)
Study
EGAS00001003298
-
Pseudotime_ordering_of_cell_cycle_state
Study
EGAS00001003293
-
The analysis of mtDNA variability of the modern Polish population
Study
EGAS00001003309
-
SLC9A3R1 variant associated with age-related hearing loss
Study
EGAS00001003072
-
MM samples for epigenomic translocation of H3K4me3 broad domains following super-enhancer hijacking
Study
EGAS00001005684
-
Modeling glioblastoma invasion using human brain organoids and single-cell transcriptomics
Study
EGAS00001003852
-
The_impact_of_the_human_leukaemia_virus_HTLV_1_on_host_gene_expression
Study
EGAS00001002259
-
HG Transcriptome sequencing in the INTERVAL cohort
Study
EGAS00001003346
-
46 patients primary malignant glioma cohort in Chinese population
Study
EGAS00001005583
-
IBD_Whole_Genome_Sequencing
Study
EGAS00001002238
-
Mutational profiling of LUAD in young never-smokers
Study
EGAS00001002773
-
Genetic characterization patients affected by Cancer of Unknown Primary
Study
EGAS00001006621
-
SDH_deficient_renal_tumours___RNA_
Study
EGAS00001004103
-
Transcriptomic response of miRNAs of monocytes to bacterial and viral stimuli assessed by RNA-seq in Africans and Europeans
Study
EGAS00001004192
-
Longitudinal therapy monitoring of ALK-positive non-small cell lung cancer (copy number, cell-free DNA)
Study
EGAS00001004276
-
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
-
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
-
Saliva microbiota in Finnish children
Study
EGAS00001003039
-
Gut metagenome/FINRISK 2002 (Salosensaari et al. Nature Comms 2021)
Study
EGAS00001005020
-
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