-
An Advanced Molecular Medicine Case Report of a Rare Human Tumor Using Genomics, Pathomics, and Radiomics
Study
phs003154
-
A comprehensive DNA methylation landscape of human and mouse cell lines derived from hematological malignancies
Study
EGAS50000000627
-
Treg cell subset-specific gene expression patterns in human head and neck cancer
Study
JGAS000135
-
Illumina HumanOmniExpress genotyping data from the TEENAGE (TEENs of Attica: Genes and Environment) study.
Study
EGAS00001000996
-
Insular Celtic population structure and genomic footprints of migration
Study
EGAS00001002769
-
Exon4-mutations in KRAS Affect MEK-ERK and Pi3K-AKT Signaling in Multiple Myeloma
Study
EGAS00001004110
-
WTCCC3 case-control study for Primary Biliary Cirrhosis
Study
EGAS00000000039
-
InterPregGen-GWAS-UZB-3
Dataset
EGAD00010001919
-
InterPregGen-GWAS-UZB-2
Dataset
EGAD00010001917
-
Exome sequencing of patient samples from study
Study
EGAS50000000171
-
Whole transcriptome seq from patient samples
Study
EGAS50000000172
-
Pan-tumor genomic biomarkers for personalization of PD-1 checkpoint blockade based immunotherapy
Study
phs001572
-
Targeted capture sequencing to identify MYC, BCL2, and BCL6 rearrangements in non-Hodgkin lymphoma
Dataset
EGAD50000000489
-
Duplex sequencing of selected breast cancer patients
Dataset
EGAD50000000769
-
Sensitive urothelial cancer detection via high volume urine DNA analysis
Dataset
EGAD50000000891
-
McQuillin_Global_WES_Schizophrenia
Dataset
EGAD50000001316
-
APC-related multiple salivary gland lesions
Study
EGAS50000001159
-
Plasma cfDNA dataset from healthy donors and cancer patients
Dataset
EGAD50000002051
-
419 Japanese healthy control
Study
JGAS000120
-
Transcriptome_Sequencing_of_Cancer_Cell_Lines
Study
EGAS00001000261
-
Whole-exome analysis of corticotropin-independent Cushing's syndrome
Study
EGAS00001000661
-
Genome sequencing of oesophagus atresia families
Study
EGAS00001004394
-
Nascent transcriptome in T-ALL bone marrow
Study
EGAS00001005864
-
Dedifferentiated_Melanoma_RNAseq
Study
EGAS00001003601
-
Targeted DNA sequencing on 37 Merkel Cell Carcinomas from New Zealand with known Merkel cell polyomavirus status
Study
EGAS00001006873
-
Discovery of cancer prognostic markers based on comparison of gene expression in colorectal cancer samples.
Study
EGAS00001005068
-
GEOCODE Cohort
Study
EGAS50000000903
-
RNA-Seq data from 34 CAF-S3 subset in human breast and ovarian cancers
Dataset
EGAD00001004810
-
Genomic and transcriptomic profiling of carcinogenesis in patients with familial adenomatous polyposis
Dataset
EGAD00001005457
-
Metadata and count matrix
Dataset
EGAD00001006435
-
scRNA-seq from brain metastasis micorenvironment and cerebrospinal fluid
Dataset
EGAD00001006452
-
Exome Atlas in HCC tumors
Dataset
EGAD00001015342
-
scTCR-seq from brain metastasis micorenvironment and cerebrospinal fluid
Dataset
EGAD00001006451
-
Single-cell transcriptome sequencing of regulatory and conventional T cells in breast cancer patients and healthy individuals.
Dataset
EGAD00001004069
-
Global RNA sequencing data of human iPSC-derived microglia from frontotemporal dementia (FTD) patients
Study
EGAS50000001688
-
Genomic Sequencing of Cervical Cancers
Study
phs000600
-
Identification of Targetable FGFR Gene Fusions in Diverse Cancers
Study
phs000602
-
Genome-Wide Analysis for Addiction Susceptibility Genes
Study
phs001266
-
NIDDK IBD Genetics Consortium Repository Immunochip
Study
phs001721
-
Discovery of Non-ETS Gene Fusions in Human Prostate Cancer using Next Generation RNA Sequencing
Study
phs000310
-
NextGen Consortium: Globin Gene Expression in Sickle Cell Genotype-Specific iPS Cells
Study
phs001212
-
Microbiome-Host Interactions in Oral Squamous Cell Carcinoma: a Metatranscriptomic Exploratory Study
Study
phs002678
-
Somatic Mutation Profile by Next Generation Sequencing in HER2+ Breast Cancer
Study
phs000770
-
Botensilimab, an Fc-enhanced Anti-CTLA-4 Antibody, is Effective Against Tumors Poorly Responsive to Conventional Immunotherapy
Study
phs003704
-
Center for Common Disease Genomics [CCDG] Neuropsychiatric: Autism Spectrum Disorder (ASD) – Whole Exomes
Study
phs002502
-
Full characterization of structural variation
Study
EGAS50000000520
-
NHLBI TOPMed - NHGRI CCDG: Pakistan Risk of Myocardial Infarction Study (PROMIS)
Study
phs001569
-
Melanoma Genome Sequencing Project
Study
phs000452
-
APOBEC3 mutagenesis drives therapy resistance in breast cancer
Study
EGAS50000000875
-
Spatial transcriptomics elucidates medulla niche supporting germinal center response in myasthenia gravis thymoma
Study
JGAS000672
-
Rapid detection of expanded short tandem repeats in personal genomics using hybrid sequencing.
Study
JGAS000002
-
LySeqST: A targeted sequencing assay for robust genomic classification of diffuse large B-cell lymphoma
Study
EGAS50000001601
-
Exome sequencing identifies mutation of the ribosome in T-cell acute lymphoblastic leukemia
Study
EGAS00001000296
-
Unifying recovery dynamics in heterogeneous diseases exemplified by COVID-19
Study
EGAS00001005735
-
The Spatial Heterogeneity in Multiple Myeloma - from the Subclonal Architecture to the Immune Microenvironment (partly hipo_K08K)
Study
EGAS00001006090
-
ERG ALTERATIONS DEFINE A NOVEL SUBTYPE OF ACUTE LYMPHOBLASTIC LEUKEMIA
Study
EGAS00001000514
-
Accurate sample assignment in a multiplexed, ultra-sensitive, high-throughput sequencing assay for minimal residual disease
Study
EGAS00001001303
-
Mapping_gene_environment_interactions_in_macrophages
Study
EGAS00001002268
-
Clonal_haematopoiesis_in_patients_with_AAA
Study
EGAS00001002873
-
A somatic reference standard for cancer genome sequencing with COLO829
Study
EGAS00001001385
-
Hermansky-Pudlak syndrome type 1 causes impaired anti-microbial immunity through a pathogenic lipid metabolism-mTOR circuit
Study
EGAS00001005053
-
Hermansky-Pudlak syndrome type 1 causes impaired anti-microbial immunity through a pathogenic lipid metabolism-mTOR circuit - 10x Genomics scRNAseq
Study
EGAS00001005098
-
Transcriptomics identifies blunted immunomodulatory effects of vitamin D in people with multiple sclerosis
Study
EGAS00001007254
-
Transcriptome of Chronic Pain and Disease
Study
phs002548
-
Characterizing TP53 and PPM1D Mutations as Resistance Drivers to Radiation Therapy in Diffuse Intrinsic Pontine Gliomas
Study
phs002380
-
Bacterial Artificial Chromosomes Establish Replication Timing and Sub-Nuclear Compartment De Novo as Extra-Chromosomal Vectors
Study
phs001520
-
Development of a diagnostic gene panel for Gorlin syndrome and its application to liquid biopsy
Study
JGAS000308
-
Comprehensive characterization of cell-free tumor DNA in plasma and urine of patients with renal tumors
Study
EGAS00001003530
-
RNA sequencing and Illumina 2.5M SNP array data collected from 675 commonly used human cancer cell lines.
Study
EGAS00001000610
-
Androgen deprivation therapy promotes an inflammatory and obesity-like microenvironment in periprostatic fat
Study
EGAS00001003286
-
Comparative transcriptome of CD34+ hematopoietic progenitors from myeloproliferative patients and control donors
Study
EGAS00001005106
-
B cell receptor repertoire kinetics after SARS-CoV-2 infection and vaccination
Study
EGAS00001005816
-
Discovery of immunotherapy targets for pediatric solid and brain tumors by exon-level expression
Study
EGAS00001007766
-
RNA-seq of high grade serous ovarian tumours
Dataset
EGAD00001009048
-
Whole genome sequencing of retinoblastoma reveals the diversity of rearrangements disrupting RB1 and uncovers a treatment related mutational signature
Dataset
EGAD00001006431
-
RNA-seq of high grade serous ovarian tumours
Dataset
EGAD00001010139
-
Whole Exome Sequencing of Pancreatic Neuroendocrine Tumors at The Human Genome Sequencing Center, Baylor College of Medicine (HGSC-BCM)
Study
phs000871
-
Genomic Analysis of Fibrolamellar Hepatocellular Carcinoma
Study
phs000828
-
Whole-Genome Sequencing Analysis of Extrachromosomal DNA with Amplicon Architect
Study
phs003100
-
Juvenile Sjogren's Syndrome (JSS) Transcriptome Study
Study
phs003048
-
The Landscape of Antisense Gene Expression in Human Cancers
Study
phs000937
-
Functionally Active Copy Number Variants Associated with Prostate Cancer Risk
Study
phs000487
-
Blood-based monitoring of relapsed/refractory cHL patients predict responses to PD-1 blockade treatment
Study
EGAS00001005894
-
Proteogenomic Analysis of CALGB40601 (ALLIANCE) a Neoadjuvant Phase III HER2-Positive Breast Cancer Trial
Study
phs003576
-
Circulating, Cell-Free DNA Methylation Patterns Indicate Cellular Sources of Allograft Injury after Liver Transplant
Study
phs003610
-
Whole Genome Sequencing Consortium on Frontotemporal Dementia With Underlying TDP-43 Pathology
Study
phs003309
-
Development of a fully human glioblastoma-in-brain-spheroid model for accelerated translational research
Study
EGAS50000000757
-
10x Multiome from Human Fetal Heart
Study
phs003778
-
Chromatin accessibility in stem cells unveils progressive transcriptional reprogramming in myelodysplastic syndrome
Study
JGAS000718
-
TGF-β signaling mediates microglial resilience to spatiotemporally restricted myelin degeneration
Study
EGAS50000001413
-
Inferring tumor genomes from peripheral blood i.e. CTCs and plasma-DNA using deep sequencing and targeted enrichment
Study
EGAS00001000337
-
Passive and active DNA methylation and the interplay with genetic variation in gene regulation
Study
EGAS00001000446
-
Advancing fast in the analysis of circulating tumour DNA
Blog
advancing-fast-in-the-analysis-of-circulating-tumour-dna
-
Youth-GEMs, the project using data to define the mental health trajectories of young people
Blog
youth-gems-mental-health
-
Somatic pathogenic variants in the normal mammary gland of sporadic breast cancer patients.
Study
EGAS00001005698
-
Analysis of mechanisms of CD19- relapse following novel low affinity CD19 Chimeric Antigen Receptor (CAR) T-cells (CD19 CAR T-cells) in a Phase I clinical study in paediatric ALL: CARPALL
Study
EGAS00001003733
-
The genetic structure of Norway
Study
EGAS00001004826
-
Assessment_of_epigenetic_variation_in_human_iPS_cells_Medip
Study
EGAS00001000741
-
Targeted sequencing of Burkitt lymphoma tumour samples from the UK's Haematological Malignancy Research Network
Study
EGAS00001004649
-
Genetic history of the Swahili population
Study
EGAS00001002569