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Whole exome sequencing of 3 primary Plasma Cell Leukemia samples
Dataset
EGAD00001005306
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WGS files for Millighan BiTE WGS
Dataset
EGAD00001005729
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WXS files for Mullighan BiTE WXS
Dataset
EGAD00001005730
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RNAseq files for Mullighan BiTE RNASEQ1
Dataset
EGAD00001005731
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lowinput RNASEQ files for Mullighan BiTE RNASEQ2
Dataset
EGAD00001005732
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combined ChIPseq (H3, modifications and TF)
Dataset
EGAD00001005969
-
Peripheral clonal expansion of T cells (scRNA-seq)
Dataset
EGAD00001005464
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Peripheral clonal expansion of T cells (scTCR-seq)
Dataset
EGAD00001005465
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WGS of B-cell lymhpoma tumor and control, HiSeq XTen sequencing, one patient, H021
Dataset
EGAD00001006057
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Primary tumor/metastatic/germline DNA trios equences files
Dataset
EGAD00001006324
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RNA-Seq samples from the BELOB clinical trial study to find transcriptome associations with response to Bevacizumab and CCNU in glioblastoma patients
Dataset
EGAD00001006329
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The application of RNA sequencing for the diagnosis and genomic classification of pediatric acute lymphoblastic leukemia
Dataset
EGAD00001006335
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RNASeq files for Mullighan TXVI dataset
Dataset
EGAD00001006609
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Single cell RNA sequencing of tumor and ascites in high grade ovarian cancer
Dataset
EGAD00001006627
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Pre and Post BCG treated bulk RNAseq dataset.
Dataset
EGAD00001006634
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Medulloblastoma whole and focused exome sequencing (n=13 patients, n=37 samples)
Dataset
EGAD00001006387
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Selenium Chemoprevention: Benefits and Harms
Study
phs002283
-
Paired Acute Myeloid Leukemia (AML) Epigenetics Study on Epialleles and Clonality
Study
phs000793
-
Improved Detection and Identification of Microsatellite Instability Features in Colorectal Cancer
Study
phs001914
-
20 years after the first human genome release. Where are we heading?
Blog
20-years-after-the-first-human-genome-release
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Insights into BRCA1 and TP53 associated breast cancer development from integrated whole genome analysis of mouse model mammary tumors
Study
EGAS50000001402
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Next-generation molecular analysis of surgical margins in oral squamous cell carcinoma for assessment of microscopic residual disease and personalized postoperative treatment decision
Study
EGAS50000000823
-
Fragmentomics profiling and quantification of plasma Epstein-Barr virus DNA enhance prediction of future nasopharyngeal carcinoma.
Study
EGAS50000000395
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A Genomics-Driven Artificial Intelligence-Based Model Classifies Breast Invasive Lobular Carcinoma and Discovers CDH1 Inactivating Mechanisms
Study
EGAS50000000485
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EGA submission account terms
Documentation
submission/terms
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Illumina HiSeqX and HiSeq 2000 whole genome sequence data on 3,001 ALS samples including 212 with known C9orf72 repeat expansions
Study
EGAS00001002598
-
ProjectMinE :llumina HiSeqX and HiSeq 2000 whole genome sequence data on 3,001 ALS samples including 212 with known C9orf72 repeat expansions
Study
EGAS00001003383
-
Illumina Omni5 SNP chip genotyping of MacTel cases and unaffected controls for a genome-wide association study
Study
EGAS00001002249
-
Single-cell RNA-sequencing of CD19 Chimeric Antigen Receptor (CAR) T-cells (CD19 CAR T-cells) from a Phase I clinical study in paediatric ALL: CARPALL
Dataset
EGAD00001010018
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Sperm sequencing reveals extensive positive selection in the human germline -WGS
Dataset
EGAD00001015592
-
Sperm sequencing reveals extensive positive selection in the human germline -NanoSeq
Dataset
EGAD00001015590
-
Sperm sequencing reveals extensive positive selection in the human germline -TargetedNanoSeq
Dataset
EGAD00001015591
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MethylScan data of plasma samples
Dataset
EGAD00001015815
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Elevated somatic mutation burdens in normal human cells due to defective DNA polymerases
Dataset
EGAD00001006212
-
Progress in Diabetes Genetics in Youth (ProDIGY) Exome Sequencing Study: SEARCH for Diabetes in Youth
Study
phs001511
-
Public Access Defibrillation Community Trial (PAD)(PAD-BioLINCC)
Study
phs003858
-
Determining Genetic Role in Treatment Response to Anti-Platelet Interventions (The PAPI Study)
Study
phs000391
-
The Role of CTCF in the Organization of the Centromeric 11p15 Imprinted Domain Interactome
Study
phs002408
-
Predicting the Prevalence of Complex Genetic Diseases from Individual Genotype Profiles Using Capsule Networks
Study
phs003146
-
CPTAC: Proteogenomic Studies of Ovarian Tumor Responses to Agents Targeting the DNA Damage Response
Study
phs003152
-
InTEAM Consortium - Alcoholic Hepatitis
Study
phs001807
-
Examination of Engineered LINE-1 Integration Events in HeLa Cells
Study
phs001669
-
The impact of CCR8+ regulatory T cells on cytotoxic T cell function in human lung cancer
Study
JGAS000454
-
Molecular characterization of invasive lobular carcinoma
Dataset
EGAD00001000288
-
Exome_trios_in_patients_with_gastroschisis
Study
EGAS00001002664
-
Comprehensive genomic profiles of small cell lung cancer
Study
EGAS00001000925
-
Regulatory T cell transcriptomic reprogramming characterizes adverse events by checkpoint inhibitors in solid tumors
Study
EGAS00001004694
-
Host pathogen interaction long read transcriptome
Study
EGAS00001006779
-
Atypical teratoid/rhabdoid tumoroids reveal subgroup-specific drug vulnerabilities WGS
Study
EGAS00001006865
-
Atypical teratoid/rhabdoid tumoroids reveal subgroup-specific drug vulnerabilities RNA-Seq
Study
EGAS00001006866
-
Atypical teratoid/rhabdoid tumoroids reveal subgroup-specific drug vulnerabilities DNA-Methylation
Study
EGAS00001006881
-
Prevention and Early Treatment of Acute Lung Injury Network - Reevaluation of Systemic Early Neuromuscular Blockade (PETAL ROSE-BioLINCC)
Study
phs003878
-
Dissecting Autoimmune Cellular and Molecular Networks in Vitiligo
Study
phs002455
-
Autosomal Recessive CD55 Deficiency is Associated with Protein Losing Enteropathy, Thrombosis, and Complement Dysregulation
Study
phs001376
-
Loss of RREB1 in pancreatic beta cells reduces cellular insulin content and affects endocrine cell gene expression
Dataset
EGAD00001009740
-
Data access policy
Dac
EGAC50000000504
-
The prevalence and clinical characteristics of TECTA-associated autosomal dominant hearing loss.
Study
JGAS000201
-
Spatial gene expression analysis of the tumor cells and their microenvironments at the pioneering-round of the metastasis.
Study
JGAS000804
-
Heterogeneity and evolution of DNA mutation rates in microsatellite-stable colorectal cancer
Study
EGAS50000000425
-
Genomic Variant Dataset of 5,309 Jeju Residents: Integrated WGS and SNP Array Analysis
Dataset
EGAD50000002451
-
Bleomycin Induced Pneumonitis WGS dataset
Dataset
EGAD50000002221
-
Transcriptomic analysis of hiPSC-derived vascular cells from CADASIL and isogenic control patient lines
Dataset
EGAD50000002181
-
RNA-seq from B-ALL patients treated on the ALLG ALL09 study
Dataset
EGAD50000001603
-
mt-scATAC-seq data and analysis
Dataset
EGAD50000001375
-
Longitudinal Transcriptomic Profiling of Endothelial Progenitor Cells in Post-COVID-19 Patients: Insights at 3 and 6-Months Post-SARS-CoV-2 Infection
Dataset
EGAD50000001452
-
Samples obtained within X-pand project
Dataset
EGAD50000001108
-
scRNA-seq dataset, RCC
Dataset
EGAD50000000566
-
Single Cell Sequencing of Medulloblastoma Samples
Dataset
EGAD50000000909
-
WES of pleomorphic lung cancer
Dataset
EGAD50000000453
-
Biomarker analysis and treatment dynamics following preoperative ipilimumab plus nivolumab in locally advanced urothelial cancer from the phase 1B NABUCCO study
Study
EGAS50000001781
-
WES and RNA sequencing of mesothelioma patients from CONFIRM clinical trial
Study
EGAS50000001814
-
Somatic copy number alterations profiling in non-small cell lung cancer and their correlation with clinical efficacy in first-line treatment
Study
EGAS50000001619
-
Long-read and short-read isoform sequencing in breast cancer
Study
EGAS00001004819
-
Amplicon based NGS of human CD4 and CD8 T cells
Study
EGAS00001004139
-
RNAseq on 20 samples of multiple myeloma patients and 3 normal plasma cells
Dataset
EGAD00001007813
-
H3K27ac/H3K27me3 landscape of medulloblastoma
Dataset
EGAD00001009709
-
Targeted NGS panel
Dataset
EGAD00001010842
-
WGS dataset of Characterization of UV DNA damage in B-cell precursor acute lymphoblastic leukemia
Dataset
EGAD00001015599
-
Warm_Autopsy_Single_Cell_X10
Dataset
EGAD00001003240
-
Aligned reads from specific genomic locations derived from Illumina HiSeqX and HiSeq2000 whole genome sequence data
Dataset
EGAD00001003513
-
Whole genome sequencing data of normal/tumors pairs from 4 patients with uterine or ovarian carcinosarcoma.
Dataset
EGAD00001003898
-
Sequencing data for Maturity-Onset Diabetes of the Young (MODY) patients in south India
Dataset
EGAD00001003919
-
Clonal expansion of mutated cell population in bladder urothelium (2018-08-03)
Dataset
EGAD00001004274
-
TCR β-chain repertoire characterization of regulatory and conventional T cells in breast tumors from breast cancer patients.
Study
EGAS00001004671
-
Finding structural variation and functional consequences from the primary leukemia cells (AML) at the single-cell level
Study
EGAS00001004903
-
Whole genome sequencing of AVM endothelial and non-endothelial cell fractions
Study
EGAS00001006719
-
scRNA-seq to study interactions between HSPCs, BMSCs and immune microenvironment
Study
EGAS00001008181
-
4 subjects, 12 brain regions, UKBEC
Dataset
EGAD00001001274
-
Cardiogenics_Custom_Pools - Agilent SureSelect
Dataset
EGAD00001000397
-
Nimblegen
Dataset
EGAD00001000398
-
Whole-genome plasma DNA sequencing in CRC patients under anti-EGFR therapy
Dataset
EGAD00001000748
-
Adeno-associated virus in the liver: natural history and consequences in tumor development
Dataset
EGAD00001004484
-
Chracterising cellur pathways underlying CD3/CD28 activation of human CD4+ cells
Dataset
EGAD00001006611
-
Clinical data
Dataset
EGAD00001006630
-
mRNA and T cell receptor sequencing of patients with Pandemrix-associated narcolepsy type 1
Dataset
EGAD00001006797
-
mRNA and T cell receptor sequencing of patients with Pandemrix-associated narcolepsy type 1
Dataset
EGAD00001006796
-
Use of Whole Genome Sequencing for Diagnosis and Discovery in the Cancer Genetics Clinic
Study
phs000942
-
Single Cell Genotypic and Phenotypic Analysis of Measurable Residual Disease in Acute Myeloid Leukemia
Study
phs003233
-
DNA methylation at HBV integrants and flanking host genomes
Study
JGAS000015
-
Atypical B cells and impaired SARS-CoV-2 neutralisation following heterologous vaccination in the elderly
Study
EGAS00001007385