-
Solution-based exome capture and HiSeq2000-based massively parallel sequencing of Follicular Lymphoma
Study
phs000729
-
Megabase-scale Haplotyped Genomic Analysis of Normal and Cancer Genomes
Study
phs000898
-
Exome Sequencing of Clear Cell Endometrial Tumors and Paired Non-tumor Samples
Study
phs000967
-
Anti-tumor and Immune Stimulatory Activity of Iberdomide in Myeloma, Including Patients with Cereblon Dysregulation
Study
EGAS50000000265
-
Patient-Derived Follicular Lymphoma Spheroids recapitulate lymph node signaling and immune profile, uncovering galectin-9 as a novel immunotherapeutic target
Study
EGAS50000000233
-
Long-term Survival Update and Extended RAS Mutational Analysis of the CAIRO2 Trial: Addition of Cetuximab to CAPOX/Bevacizumab in Metastatic Colorectal Cancer
Study
EGAS50000000775
-
Sequencing data for the manuscript "Resolving spatial subclonal genomic heterogeneity of loss of heterozygosity and extrachromosomal DNA in gliomas"
Dataset
EGAD50000001394
-
Fragmentomics profiling and quantification of plasma Epstein-Barr virus DNA enhance prediction of future nasopharyngeal carcinoma.
Dataset
EGAD50000001449
-
Single-cell RNA-Seq analysis of thymic ILC1 progenitors and NK cell differentiation This analysis involved a multiplexed sequencing run to study thymic innate lymphoid cells (ILCs) and NK progenitors. The generated data requires a demultiplexing file to separate and identify the individual sample tags for downstream analysis.
Dataset
EGAD50000001157
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Genome Sequencing and Variant Calling of HCM Patients with MYH7 Variants
Study
phs004024
-
WGS of Five Pancreatic Cancer Patients-Tumor and Normal
Study
phs003775
-
Multiple paralogues and recombination mechanisms contribute to the high incidence of 22q11.2 Deletion Syndrome
Study
EGAS50000000601
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DAC for human-derived clonal organoid studies
Dac
EGAC50000000628
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Identification of genetic mutations characteristic for recurrence and metastasis of lymphoma.
Study
JGAS000087
-
Identification of genetic mutations characteristic for recurrence and metastasis of gastric cancer.
Study
JGAS000086
-
Variant calling for IMMU-SCCHN1 cohort
Dataset
EGAD50000002205
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Whole Exome Sequencing of cohorts of Mutant Braf mouse model melanoma DNA and germline DNA.
Study
EGAS00001000729
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Cerebrospinal fluid circulating tumour DNA allows the characterisation and monitoring of medulloblastoma
Study
EGAS00001004651
-
Multi-region RNA sequencing of tumour regions and tumour-adjacent normal lung tissue
Study
EGAS00001006517
-
Smart-seq3 scRNA-seq of cells from primary (OV2295) and metastatic (OV2295R2) high-grade serous ovarian cancer cell-line
Study
EGAS00001006868
-
Genomic characterization of co-existing biliary tract intraepithelial neoplasia and carcinoma lesions reveals distinct evolutionary paths of gallbladder cancer
Dataset
EGAD00001007792
-
single cell RNA sequencing of resting and IAV-stimulated mononuclear phagocytes of Africans and Europeans
Dataset
EGAD00001006938
-
small RNA-sequencing and RNA-sequencing of human brain tissue with temporal lobe epilepsy
Dataset
EGAD00001005735
-
Facioscapulohumeral muscular dystrophy (FSHD): RNA-seq of isogenic TIRM+, TIRM- muscle and PBMCs from patients and matched controls
Dataset
EGAD00001011077
-
WES and RNA-seq data of 11 cancer patients with multiple cancer types
Dataset
EGAD00001010169
-
Human normal esophagus and Barrett's esophagus mtDNA sequencing
Dataset
EGAD00001008310
-
Single-Cell DNA Methylation Profiling via scTAMseq
Dataset
EGAD00001015498
-
Discovery of resistance mechanisms to the BRAF inhibitor vemurafenib in metastatic BRAF mutant melanoma
Dataset
EGAD00001001046
-
RNAseq - Discovery of resistance mechanisms to the BRAF inhibitor vemurafenib in metastatic BRAF mutant melanoma
Dataset
EGAD00001001050
-
Adenoma development in familial adenomatous polyposis and MUTYH‐associated polyposis: somatic landscape and driver genes
Dataset
EGAD00001004332
-
Genomic and transcriptomic determinants of therapy resistance and immune landscape evolution during anti-EGFR treatment in colorectal cancer
Dataset
EGAD00001004501
-
Whole genome sequencing libraries from the study "Histological Transformation and Progression in Follicular Lymphoma: a Clonal Evolution Study".
Dataset
EGAD00001002897
-
Non-coding RNAs Activated by the Wnt/Beta-catenin Signaling Pathway in Hepatoblastoma
Study
phs001433
-
Mitochondrial DNA deletion detection in POLG patients
Study
phs002052
-
Investigating the Role of Neddylation in the Repair of Topoisomerase I-Mediated DNA Damage in Colorectal Cancer
Study
phs003257
-
Center for Inherited Disease Research (CIDR)-National Institute on Aging (NIA) Whole Exome Analysis of Ehlers-Danlos Syndrome
Study
phs001779
-
NINDS Deep Sequencing for the Detection of Viral Sequences in Primary Progressive Multiple Sclerosis Brains
Study
phs000715
-
Chromatin Landscape of BET Inhibitor-Treated CD8+ T-cells from Chronic Lymphocytic Leukemia Patients
Study
phs003613
-
Toxigenic Clostridium perfringens isolated from at-risk pediatric inflammatory bowel disease patients
Study
EGAS50000000334
-
Transcriptional Response to Hypoxia in iPSC-Derived Endothelial Cells from a High Altitude Adapted Population
Study
phs003758
-
Genomics of Substance Use Disorders in Latin American Populations
Study
phs003558
-
Germline Genomic Analyses of Breast Cancer in Latinas
Study
phs003144
-
Clonal Lineage Tracing of Primary Human Cortical Progenitors, Cell Type Profiles in the Brain Vasculature and Genotyping Data for 22q11DS and Control iPS Lines
Study
phs002624
-
High Frequency Ventilation in Premature Infants (HIFI-BioLINCC)
Study
phs004032
-
Somatic Mutation in Normal Bladder Study
Study
phs004105
-
Center for Common Disease Genomics [CCDG] - Neuropsychiatric: Epilepsy: Epi25 Consortium
Study
phs001489
-
Genome and gene analysis of gastrointestinal cancer and elucidation of its clinicopathological significance
Study
JGAS000233
-
The EGA at the International Congress of Human Genetics
Blog
the-ega-at-the-international-congress-of-human-genetics
-
Stromal-induced epithelial-mesenchymal transition induces drug resistance in acute lymphoblastic leukemia
Study
EGAS00001006120
-
Tracing the origin of disseminated tumor cells in breast cancer using single-cell sequencing
Study
EGAS00001002102
-
The Genomic Landscape of Response to EGFR Blockade in Colorectal Cancer
Study
EGAS00001001305
-
Enhanced detection of circulating tumor DNA by fragment size analysis
Study
EGAS00001003258
-
Genome wide association study on coronary heart disease in patients with familial hypercholesterolemia
Study
EGAS00001000734
-
Transcriptional_profiling_of_tauopathies_in_human_IPS_derived_neurons
Study
EGAS00001000382
-
Altered oligodendrocyte heterogeneity in Multiple sclerosis revealed by single nuclei RNA sequencing
Study
EGAS00001003412
-
Persistence of circulating tumor DNA in breast cancer patients during neoadjuvant treatment is a significant predictor of poor tumor response
Study
EGAS00001005798
-
Profiling the unique protective properties of intracranial arterial endothelial cells
Study
EGAS00001004479
-
BCR Signaling in human BM PC
Study
EGAS00001004948
-
Whole genome sequencing of tumor samples from advanced pre-treated NSCLC patients recruited in a phase I/II single-arm trial utilising CVA21, an oncolytic coxsackie virus, in combination with pembrolizumab.
Study
EGAS00001008258
-
Single-cell decoding of drug induced transcriptomic reprogramming in triple negative breast cancers
Study
EGAS00001007242
-
SLCO1B1 Variants and Methotrexate Clearance
Study
phs000426
-
Center for Common Disease Genomics [CCDG] - Neuropsychiatric: Victorian Collaborative AuTism Study (CATS): Family and Community Study of the Genetics of Autism Spectrum Disorder
Study
phs002044
-
ILyAD (Indolent Lymphoma And vitamin D)
Study
phs003503
-
Single Cell and Spatial Transcriptomic Profiling of Haemophilus ducreyi Infection
Study
phs003754
-
Study on the Genetics of Alcoholism (COGA): Smoke Screen and Exome Sequencing
Study
phs001208
-
Whole-genome and transcriptome versus panel sequencing in precision oncology: A translational-clinical comparison
Study
EGAS50000000431
-
Singel-cell RNA sequencing and CUT&RUN sequencing of human RUNX2-deficient osteoblasts
Study
JGAS000663
-
Biallelic tumor suppressor loss and DNA repair defects in de novo small cell prostate cancer
Study
EGAS00001003007
-
Single-cell DNA amplicon sequencing reveals clonal heterogeneity and evolution in T-cell acute lymphoblastic leukemia
Study
EGAS00001004440
-
Transcriptional profiling of ovarian tumours and cell lines
Study
EGAS00001004814
-
Novel optineurin frameshift insertion causing familial frontotemporal dementia and parkinsonism without amyotrophic lateral sclerosis
Study
EGAS00001005220
-
Center for Common Disease Genomics (CCDG) Neuropsychiatric: Multimodal Developmental Neurogenetics of Females
Study
phs002043
-
Male Infertility: Genetics of Spermatogenic Failure
Study
phs001023
-
Center for Common Disease Genomics [CCDG] - Neuropsychiatric: Genomics of Autism Spectrum Disorder (GASD)
Study
phs002509
-
Center for Common Disease Genomics (CCDG) Neuropsychiatric: Homozygosity Mapping Consortium for Autism (HMCA)
Study
phs001894
-
Center for Common Disease Genomics [CCDG] - Neuropsychiatric: Simons Searchlight
Study
phs002512
-
QUANTitative Chest Computed Tomography UnMasking Emphysema Progression in Alpha-1 Antitrypsin Deficiency
Study
phs000698
-
Center for Common Disease Genomics (CCDG) Neuropsychiatric: Autism Center of Excellence (ACE II)
Study
phs002042
-
Center for Common Disease Genomics (CCDG) Neuropsychiatric: Study of Autism Genetics Exploration (SAGE)
Study
phs001740
-
The Library of Integrated Network-Based Cellular Signatures (LINCS) - NeuroLINCS
Study
phs001231
-
Center for Common Disease Genomics (CCDG)-Neuropsychiatric: A Study of the Genetic Causes of Complex Pediatric Disorders (CAG)
Study
phs002004
-
Center for Common Disease Genomics (CCDG) Neuropsychiatric: Autism Genetic Resource Exchange
Study
phs001766
-
Whole genome and transcriptome sequencing of lung cancer patients and cell lines at Genentech
Study
phs000299
-
Small Intestine Neuroendocrine Tumors (Carcinoid Tumors)
Study
phs000579
-
Center for Common Disease Genomics (CCDG) Neuropsychiatric: The Autism Simplex Collection (TASC)
Study
phs001741
-
A Phase I Study with a Personalized Neoantigen Cancer Vaccine in Melanoma
Study
phs001451
-
Trisomy 21 Dosage Compensation Map (T21DoCoMap)
Study
phs002397
-
Prostate Cancer Upgrading Reference Set
Study
phs003670
-
Gut metagenome associations with extensive digital health data in a volunteer-based EstMB cohort second timepoint data
Study
EGAS50000001181
-
Characterization of HCV-specific CD4 T cells during DAA-Therapy
Study
EGAS00001003950
-
Negligible impact on missing heritability of autoimmune-locus rare coding-region variants
Study
EGAS00001000476
-
The evolutionary history of human colitis-associated colorectal cancer
Study
EGAS00001003028
-
Preclinical Pediatric Molecular Analysis for Therapy Choice (MATCH)
Study
EGAS00001008011
-
Whole genome study of Hurthle cell thyroid carcinoma
Study
EGAS00001000940
-
GCAT | Genomes for life: cohort study of the genomes of Catalonia
Study
EGAS00001003018
-
The Medical Genome Reference Bank: a whole genome data resource of 4,000 healthy elderly individuals.
Study
EGAS00001003511
-
Prostate cancer ancestral genomic disparity
Study
EGAS00001006425
-
Whole-genome sequencing of normal Singaporean volunteers
Study
EGAS00001004007
-
Differentially methylated CpGs in response to growth hormone administration in children with idiopathic short stature
Study
EGAS00001006115
-
Liquid biopsy for molecular characterization of diffuse large B-cell lymphoma and early assessment of minimal residual disease
Study
EGAS50000000215