-
Single-cell sequencing data from AIM⁺ HIV-1-specific T cells in post-intervention controllers and non-controllers
Study
EGAS50000001570
-
Tumor-derived cell lines as pharmacogenomic models to predict therapeutic vulnerabilities in hepatocellular carcinoma
Dataset
EGAD00001004938
-
Target-capture sequencing of FFPE tumor samples from patients diagnosed with NKTL
Dataset
EGAD00001005303
-
Exome sequencing of a Novel Primary T Cell Immunodeficiency Kindred (2019-08-19)
Dataset
EGAD00001005263
-
A Tumour Organoid Biobank for Mapping Cancer Cell Vulnerabilities - RNA
Dataset
EGAD00001015470
-
Genomic Evolution of Breast Cancer Metastasis and Relapse
Dataset
EGAD00001002698
-
Germline and somatic variants in myelodysplastic syndrome and therapy-related myeloid neoplasms
Dataset
EGAD00001004861
-
WGS data of patients diagnosed with NKTL
Dataset
EGAD00001005231
-
Spatial whole exome sequencing of metastatic melanoma
Dataset
EGAD00001005819
-
MYOSEQ
Dataset
EGAD00001006158
-
A108759B
Dataset
EGAD00001007088
-
Organoid Derivation Project - WGS (2024-10-14)
Dataset
EGAD00001015424
-
Genomic and immune signatures predict clinical outcome in newly diagnosed multiple myeloma treated with immunotherapy regimens
Dataset
EGAD00001011132
-
Complex structural variation patterns in pediatric solid tumors WGS
Dataset
EGAD00001011378
-
The G2 gene expression signature and MYC overexpression are independent poor prognostic factors in childhood high-grade osteosarcoma
Dataset
EGAD00001015503
-
LCM_WGS__Thyroid_
Study
EGAS00001007913
-
HLA-A*3101 and Carbamazepine-Induced Hypersensitivity Reactions in Europeans
Study
EGAS00000000036
-
Osteosarcoma_Sequencing
Study
EGAS00001000013
-
ADCC_Rearrangement_Screen
Study
EGAS00001000030
-
Various_Cancer_Fusion_Gene_Sequencing
Study
EGAS00001000012
-
Table of gene-level RNA counts from newborn screening dried blood spot samples
Dataset
EGAD00010001707
-
3q-capture DNA sequencing of primary AMLs with 3q26 rearrangements
Dataset
EGAD00001006820
-
SCANDARE MACARON project
Dac
EGAC50000000104
-
Exome sequencing of early and late passage Patient Derived Xenogratf Tumoroids with matched Patient Derived Xenogratfs and matched normal liver
Dataset
EGAD50000000266
-
Cell-Free DNA Genomic Profiling and its Clinical Implementation in Advanced Prostate Cancer
Dataset
EGAD50000000348
-
RNA-Seq data from tumor samples collected from 12 UTSW translocation renal cell carcinoma (tRCC) patients.
Study
EGAS50000000127
-
ScRNA sequencing and snp-array genotyping of peripheral immune cells in Type 1 diabetes mellitus (T1DM)
Dataset
EGAD50000000345
-
Sensitive circulating tumor DNA based residual disease detection in epithelial ovarian cancer
Study
EGAS50000000245
-
Whole Exome Sequencing
Study
EGAS50000000259
-
Molecular underpinnings of dedifferentiation and aggressiveness in chromophobe renal cell carcinoma
Study
EGAS50000000287
-
RNA-seq following miR-130a knock-down (KD) in Flag-tag AML1-ETO Kasumi-1 cells
Study
EGAS00001005866
-
Whole genome sequencing of pheochromocytoma and paraganglioma arising from germline SDHB mutations
Dataset
EGAD50000000502
-
Clonal Evolution and Blastic Plasmacytoid Dendritic Cell Neoplasm - Two Cases
Study
EGAS50000000214
-
Brazilian Thyroid WES
Dataset
EGAD50000000086
-
DAC for a single-cell multi-omic atlas of nodal B-cell non-Hodgkin lymphomas
Dac
EGAC50000000226
-
Mate-pair sequencing of 12q-amplified osteosarcomas
Study
EGAS50000000493
-
Non_Hodgkin_lymphoma_project___mutational_burden_of_chemotherapy_in_normal_blood
Study
EGAS00001006733
-
RNA sequencing data from 10 patient derived colorectal cancer organoids
Dataset
EGAD50000000962
-
Complement C1s deficiency in a male Caucasian patient with systemic lupus erythematosus: A case report
Study
EGAS50000000707
-
FOCUS Trial
Study
EGAS50000000725
-
cfDNA methylation profiling on longitudinally collected blood plasma of patients with esophageal adenocarcinoma
Study
EGAS50000000514
-
Comprehensive molecular portrait reveals genetic diversity and distinct molecular subtypes of small intestinal neuroendocrine tumors
Study
EGAS50000000642
-
T-bet+ CXCR3+ B cells drive hyperreactive B-T cell interactions in multiple sclerosis
Dac
EGAC50000000464
-
Transcriptomic changes in amniotic fluid associated with the fetal inflammatory response
Study
EGAS50000000866
-
RNASeq from PPGL-derived PC12 cell lines cultivated in normoxia and hypoxia conditions.
Study
EGAS50000000814
-
SUM-seq data for Primary T-cells differentiated to helper subtypes
Dataset
EGAD50000001204
-
Germline WES of serrated polyposis syndrome
Study
EGAS50000000765
-
Identification Of Pathogenic Mutations And Application Of Polygenic Risk Scores In Early-Onset Diabetes Patients
Study
EGAS50000000991
-
SCANDARE ovarian WES data
Dataset
EGAD50000001658
-
Study assessing the efficacy and safety of durvalumab plus olaparib plus fulvestrant in selected metastatic or locally advanced ER-positive, HER2-negative breast cancer patients.
Study
EGAS50000001166
-
Whole-genome sequencing data of human hematopoietic stem and progenitor cells in post-transplant clonal hematopoiesis
Dataset
EGAD50000001347
-
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
-
Genomic characterization of germ-cell tumors in childhood
Study
EGAS50000000619
-
WES of sorted B lineage cells from patients with plasma cell neoplasms
Study
EGAS50000001498
-
VariantMedium: Sensitive and generalizable somatic point mutation calling with 3D DenseNets trained and evaluated on experimental confirmation data
Study
EGAS50000001661
-
The genomic landscape of large and small tumors in early-onset prostate cancer patients
Study
EGAS00001000383
-
ISCAPE V(D)J libraries from HA-specific single memory B cells of four Influenza A exposed individuals
Dataset
EGAD50000002019
-
High-depth whole genome sequencing of paired ductal carcinoma in-situ (DCIS) and germline control samples from 51 individuals.
Dataset
EGAD50000002071
-
Meta-analysis of Genome-Wide-Association Sudies for plasma Factor XI
Study
EGAS00001002123
-
Novel manifestations of immune dysregulation and granule defects in gray platelet syndrome
Study
EGAS00001004216
-
Inherited damaging mutations in immune-related genes favour the development of genetically heterogeneous synchronous colorectal cancer.
Study
EGAS00001001461
-
Breast_Cancer_Exome_Resequencing
Study
EGAS00001000207
-
Integrated Molecular Profilting in Advanced Cancers Trial
Study
EGAS00001001897
-
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
-
Mutational profiling of LUAD in young never-smokers
Study
EGAS00001002773
-
Whole_Genome_sequencing_of_individuals_from_Val_Borbera__Italy
Study
EGAS00001000458
-
Long-read sequencing for cell-free DNA analysis (human)
Study
EGAS00001006328
-
Transcriptomic response of miRNAs of monocytes to bacterial and viral stimuli assessed by RNA-seq in Africans and Europeans
Study
EGAS00001004192
-
Pseudotime_ordering_of_cell_cycle_state
Study
EGAS00001003293
-
Modeling glioblastoma invasion using human brain organoids and single-cell transcriptomics
Study
EGAS00001003852
-
HipSci HumanExome BeadChip analysis - Usher syndrome and congenital eye defects
Study
EGAS00001002008
-
SDH_deficient_renal_tumours___RNA_
Study
EGAS00001004103
-
HipSci HumanExome BeadChip analysis - Bleeding and Platelet disorders
Study
EGAS00001002013
-
HipSci HumanHT 12 Expression BeadChip analysis - Hereditary Spastic Paraplegia
Study
EGAS00001002021
-
HipSci___Whole_Exome_sequencing___Usher syndrome and congenital eye defects
Study
EGAS00001001985