-
Bisulfite-converted duplexes for the strand-specific detection and quantification of rare mutations
Study
EGAS00001002406
-
Single cell genomic variation induced by mutational processes in cancer
Study
EGAS00001006343
-
Method to Assess Lung Water Accumulation During Exercise
Study
phs003346
-
Whole-Exome Sequencing Study of Diabetic Nephropathy
Study
phs003429
-
Development of Novel Synovial Sarcoma Organoids Models for Drug Discovery
Study
JGAS000806
-
Genetic insights into the biological mechanisms governing human ovarian ageing
Study
EGAS00001004947
-
NHLBI TOPMed: Children's Health Study (CHS) Integrative Genetic Approaches to Gene-Air Pollution Interactions in Asthma (GAP)
Study
phs001602
-
Metagenomic Deep Sequencing in Meningitis and Encephalitis
Study
phs001067
-
Gene expression adaptation of metastases to their host tissue
Study
EGAS50000000817
-
Analysis of four key cell types (epithelial, fbroblast, myeloid and T cells)
Study
EGAS00001003579
-
Analysis of translatome, truncating mutations, lncRNA, circRNA and microproteins of 80 human DCM cases and controls
Study
EGAS00001003263
-
Molecular stratification of endometrioid ovarian carcinoma predicts clinical outcome
Study
EGAS00001004366
-
TRACERx NSCLC - whole genome sequencing for ctDNA study
Dataset
EGAD50000000452
-
RB1 Loss Triggers Dependence on ESRRG in Retinoblastoma
Study
phs002859
-
Childhood Cancer Data Initiative (CCDI): CCDI Pediatric In Vivo Testing Program - Leukemia
Study
phs003164
-
Mutational Spectrums and Clinical Features of Patients with LOXHD1 Variants Identified in a 8,074 Hearing Loss Patient Cohort.
Study
JGAS000192
-
Understanding the genetic risk underlying racial disparities in uterine fibroids
Study
phs001409
-
Whole exome sequencing and RNA sequencing of lineage-switched acute myeloid leukemia with KMT2A-AFF1 rearrangement
Study
JGAS000631
-
Familial_Thrombocytosis_germline_exome_sequencing
Study
EGAS00001000088
-
ET_Exome
Study
EGAS00001000102
-
Exome sequencing of a Novel Primary T Cell Immunodeficiency Kindred (2019-08-19)
Dataset
EGAD00001005263
-
A New Reference Panel to Boost African American Genotype Imputation
Study
phs001798
-
Methylation biomarker study of magnesium deficiency and colorectal cancer
Study
phs002037
-
Identification_and_functional_validation_of_driver_mutations_in_colorectal_cancer
Study
EGAS00001000044
-
Cloning of the breakpoint of a novel translocation associated with T-acute lymphoblastic leukaemia
Dataset
EGAD00001002193
-
GTestimate: Improving relative gene expression estimation in scRNA-seq using the Good-Turing estimator
Study
EGAS50000000915
-
Hypothalamic transcriptome in Prader-Willi syndrome
Study
EGAS00001002901
-
Whole-exome Sequencing Combined with Functional Genomics Reveals Novel Candidate Driver Cancer Genes in Endometrial Cancer
Study
EGAS00001000318
-
WES of 2 human osteosarcoma and corresponding cell lines
Study
EGAS00001003923
-
EGAS00001001311_MalariaGEN_GWAS_summary_statistics_2015
Dataset
EGAD00010001081
-
Germline DNMT3A mutation in familial acute myeloid leukemia
Dataset
EGAD00001006248
-
OSCC WES and genomes
Dataset
EGAD00001006077
-
Integrated Transcriptomic and Regulatory RNA Profiling Reflects Complex Pathophysiology and Uncovers a Conserved Gene Signature in End Stage Heart Failure RNA-Seq data
Study
EGAS50000000810
-
RNA-seq data of bone marrow CD34-positive cells from 57 patients with myelodysplastic syndromes (MDS) and 5 healthy individuals (62 participants in total)
Study
JGAS000724
-
DNA and RNA Profiling Using Simultaneous Sequencing (Simul-seq)
Study
phs001214
-
Pulmonary Fibrosis and Telomerase Dysfunction
Study
phs002692
-
Genomic Characterization of African-American Prostate Cancer
Study
phs000945
-
Genomic analysis of HGSOC using long read sequencing
Study
EGAS50000001036
-
Identification of therapeutic target molecules for prostate cancer by using next generation sequencer
Study
JGAS000198
-
RNAseq___Discovery_of_resistance_mechanisms_to_the_BRAF_inhibitor_vemurafenib_in_metastatic_BRAF_mutant_melanoma
Study
EGAS00001000813
-
Discovery_of_resistance_mechanisms_to_the_BRAF_inhibitor_vemurafenib_in_metastatic_BRAF_mutant_melanoma
Study
EGAS00001000812
-
Mid-pass Whole-genome Sequencing in a Malagasy Cohort Uncovers Body Composition Associations
Study
EGAS50000000496
-
CRISPR screening in human trophoblast stem cells reveals both shared and distinct aspects of human and mouse placental development
Study
JGAS000659
-
Guardians of the genome: protecting DNA from endogenous sources of damage
Dataset
EGAD00001006055
-
Next generation sequencing of diffuse intrinsic pontine glioma samples to identify recurrent mutations, variations, and expression patterns to define novel therapies
Study
phs001526
-
Germline hypomorphic CARD11 mutations in severe atopic disease
Study
phs001369
-
Drug Development against Tumor Microtube Networks in Glioblastoma
Study
EGAS50000000477
-
NHLBI TOPMed: Genetic Epidemiology Network of Salt Sensitivity (GenSalt)
Study
phs001217
-
Celiac disease meta-analysis
Study
EGAS00001003805
-
The ALT pathway generates telomere fusions that can be detected in the blood of cancer patients
Dataset
EGAD00001012101
-
Precision Diagnosis of Neurodevelopmental Disorders in Middle Eastern Populations
Study
phs003917
-
Geriatric Oncology Database of genotypes and methylation, gene expression, clinical data, and survey results on psychosocial and physical conditions in Japanese elderly cancer patients to establish truly effective treatment strategy
Study
JGAS000061
-
Meta-analysis of Genome-Wide-Association Sudies for plasma Factor XI
Study
EGAS00001002123
-
Splenic_Marginal_Zone_Lymphoma_with_villous_lymphocytes_exome_sequencing
Study
EGAS00001000139
-
Multiomics Characterization of Low-grade Serous Ovarian Carcinoma
Study
EGAS00001004724
-
Development of Novel Histiocytic Sarcoma Organoid Model for Drug Discovery
Study
JGAS000807
-
A novel recurrent mutation in MITF predisposes to familial and sporadic melanoma
Study
phs000419
-
An RCOR1 loss-associated gene expression signature identifies a prognostically significant DLBCL subgroup
Study
EGAS00001001000
-
Gabriella Miller Kids First Pediatric Research Program: An Integrated Clinical and Genomic Analysis of Treatment Failure in Pediatric Osteosarcoma
Study
phs001714
-
Integrated Single-Cell Genetic and Transcriptional Analysis Suggests Novel Drivers of Chronic Lymphocytic Leukemia
Study
phs001372
-
Whole exome and transcriptome analysis of UV-exposed epidermis and carcinoma in situ reveals early drivers of carcinogenesis
Study
phs002019
-
HiChIP for 2 samples
Dataset
EGAD50000001787
-
Whole Genome Bisulfite sequencing data for Oncogenic 3D genome conformations identify novel therapeutic targets in ependymoma
Dataset
EGAD00001008805
-
Novel driver variants in the histone 3.3 genes, H3F3A and H3F3B, define bone and cartilage cancer sub-types
Dataset
EGAD00001000646
-
Whole genome sequencing data of paediatric KMT2A-rearranged acute lymphoblastic leukemia
Study
EGAS50000001079
-
Single-nucleus transcriptomic profiling of aging Down Syndrome brains
Study
EGAS00001005691
-
Pre-Existing Skin-Resident CD8 and γδ T Cell Circuits Mediate Immune Response in Merkel Cell Carcinoma and Predict Immunotherapy Efficacy
Study
phs003629
-
A system-wide approach to monitor responses to synergistic BRAF and EGFR inhibition in colorectal cancer cells
Study
EGAS00001002654
-
RNA-sequencing of six Pilocytic astrocytoma tumors
Study
EGAS00001002149
-
A study of resistance to novel coronavirus infection in health care workers
Study
JGAS000562
-
Homozygous loss-of-function variants in European cosmopolitan and isolate populations
Study
EGAS00001001606
-
Whole exome sequencing of trio with primary immunodeficiency (IL2RB)
Dataset
EGAD00001004963
-
Functional Analysis of Genetic Variants in African Americans with Breast Cancer
Study
phs002977
-
Mutations conferring differential treatment response in breast cancer
Study
EGAS00001003626
-
RNA-seq dataset: Single-cell spatial analysis of pediatric high-grade glioma reveals a novel population of immunosuppressive and tumor-promoting SPP1+/GPNMB+ myeloid cells
Dataset
EGAD00001015450
-
Next Generation Mendelian Genetics: Familial Combined Hyperlipidemia
Study
phs000538
-
Autosomal recessive
Study
phs000848
-
Gene Fusion Discovery through RNA Sequencing of Human Glioblastoma Stem Cell Lines
Study
phs000505
-
Autosomal Recessive PGM3 Mutations Link Glycosylation Defects to Atopy, Immune Deficiency, Autoimmunity, and Neurocognitive Impairment
Study
phs000809
-
FusionSeq: a modular framework for finding gene fusions by analyzing Paired-End RNA-Sequencing data
Study
phs000311
-
Meta-Analysis of Genome-Wide Association Studies of Bladder Cancer Risk
Study
phs003342
-
CML_blast_phase_rearrangement_screen
Study
EGAS00001000191
-
RAG mediated recombination is the predominant driver of oncogenic rearrangement in ETV6-RUNX1 Acute Lymphoblastic Leukemia (Rearrangement_sequencing_data)
Dataset
EGAD00001000635
-
RAG mediated recombination is the predominant driver of oncogenic rearrangement in ETV6-RUNX1 Acute Lymphoblastic Leukemia (Whole_Genome_sequencing_data)
Dataset
EGAD00001000634
-
RAG mediated recombination is the predominant driver of oncogenic rearrangement in ETV6-RUNX1 Acute Lymphoblastic Leukemia (Whole_exome_sequencing_data)
Dataset
EGAD00001000636
-
Reference Standards for Mosaic Variant Detection
Study
phs003399
-
Integration of genomics and histology reveals diagnosis and effective therapy of refractory cancer of unknown primary with PDL1 amplification (H021)
Study
EGAS00001001846
-
CTCF ChIP-sequencing data for Oncogenic 3D genome conformations identify novel therapeutic targets in ependymoma
Dataset
EGAD00001008806
-
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
-
MYO5B mutations in Pheochromocytoma/Paraganglioma promote cancer progression
Study
EGAS00001003991
-
mRNA capture sequencing and RT-qPCR for the detection of pathognomonic, novel and secondary fusion transcripts in formalin-fixed paraffin-embedded tissue: a sarcoma showcase
Dataset
EGAD00001007696
-
Mesothelioma Genomics Study - WGS tumour/normal pairs
Study
EGAS00001002299
-
Human adipose tissue immune cells
Study
EGAS00001003725
-
Genomic Features of Lung Adenocarcinoma from Individuals with <= 10 Pack-Year Smoking History
Study
phs002556
-
Single-Cell Transcriptomics of Adult Recurrent Respiratory Papillomatosis
Study
phs003349
-
High-resolution profile of neoantigen-specific TCR activation links moderate stimulation to increased resilience of engineered TCR-T cells
Study
EGAS50000000600
-
Pancreatic cancer organoids recapitulate disease and allow personalized drug screening
Study
EGAS00001003369
-
Ion Proton WES raw and processed data from and novel immunodeficiency proband.
Dataset
EGAD50000000524
-
Identification of ALS Associated Genes Using Whole Genome Sequencing
Study
phs001585
-
ESGI-Identification of novel genes and mechanisms leading to Primary Ciliary Dyskinesia
Dataset
EGAD00001001092