-
Methylation Profiles of Cell-Free DNA Using Nanopore Sequencing
Study
phs002950
-
Genomic analysis of primary plasma cell leukemia reveals complex structural alterations and high risk mutational patterns
Study
phs002022
-
Sexual dimorphism in human immune system aging
Study
phs001934
-
Single-Cell Multi-Omic Analysis of the Vestibular Schwannoma Ecosystem Uncovers a Nerve Injury-Like State
Study
phs003318
-
A Human Lymphoma Organoid Model for Evaluating and Targeting the Follicular Lymphoma Tumor Immune Microenvironment
Study
phs003410
-
Genomic Tumor Correlates of Clinical Outcomes Following Organ-Sparing Chemoradiation Therapy for Bladder Cancer
Study
phs003402
-
NHLBI TOPMed - NHGRI CCDG: Malmo Preventive Project (MPP)
Study
phs001544
-
Sequencing Lymphoma
Study
phs001229
-
Pediatric Preclinical Testing Consortium (PPTC)
Study
phs001437
-
Shotgun Transcriptome and Isothermal Profiling of SARS-CoV-2 Infection Reveals Unique Host Responses, Viral Diversification, and Drug Interactions
Study
phs002258
-
Genetic Analysis of Skin Cells
Study
phs003282
-
Gene Variants in Pheochromocytoma and Paraganglioma
Study
phs002405
-
The Contribution of De Novo Coding Mutations to Meningomyelocele
Study
phs003746
-
Transgenerational Transmission of Post-Zygotic Mutations Suggests Symmetric Contribution of First Two Blastomeres to Human Germline
Study
phs003781
-
Spatiotemporal immune atlas of the first clinical-grade gene-edited pig-to-human kidney xenotransplant
Study
EGAS50000000244
-
"Distinct immunometabolic signatures in circulating immune cells define disease outcome in acute-on-chronic liver failure"
Study
EGAS50000000391
-
Genomic Alterations and Transcriptional Phenotypes in Circulating Tumor DNA and Matched Metastatic Tumor
Study
phs003689
-
Spatiotemporal Charting of Human Esophageal Development for Epidermolysis Bullosa Cell Therapy
Study
phs003281
-
Childhood Cancer Data Initiative (CCDI): Pediatric In Vivo Testing Program - Neuroblastoma
Study
phs003163
-
Multiplexed scRNA-Seq Reveals Cellular and Genetic Correlates of SLE
Study
phs002812
-
Immediate Postoperative Minimal Residual Disease Detection with MAESTRO Predicts Recurrence and Survival in Head and Neck Cancer Patients Treated with Surgery
Study
phs003981
-
Identification and characterization of tertiary lymphoid structures in brain metastases
Study
EGAS50000000563
-
P4HA1 Mediates Hypoxia-Induced Invasion in Human Pancreatic Cancer Organoids
Study
phs003961
-
Human papillomavirus integration induces oncogenic host gene fusions in oropharyngeal cancers
Study
EGAS50000000892
-
Estimating the Efficacy of Pharmacogenomics Over a Lifetime
Study
phs003454
-
High volume culture initiating in vitro evolution in neuroblastoma cell lines
Study
EGAS00001007962
-
Single Cell DNA Methylation Analysis for Forensic Epigenetics
Study
phs003204
-
Disease-Linked Regulatory DNA Variants and Homeostatic Transcription Factors in Epidermis
Study
phs003977
-
Transcriptome of human trophoblast stem cells derived from normal and HDP placentas
Study
JGAS000660
-
RNA sequencing of surgically removed lung adenocarcinoma afterwards treated with immune checkpoint inhibitors
Study
JGAS000675
-
Identification of a Type 1 Diabetes-Associated T Cell Receptor Repertoire Signature from the Human Peripheral Blood
Study
phs003979
-
End motifs analysis of circulating DNA from the plasma of patients with stage II-III breast cancer (n=50), stage I-III non-small cell lung cancer (n=56), metastatic colorectal cancer (mCRC) (n=15) and healthy individuals (n=37)..
Study
EGAS50000001319
-
ProstOmics: spatial and bulk multi-omics of prostate cancer
Study
EGAS50000000413
-
Dynamic Evolution of Fibroblasts Revealed by Single Cell RNA Sequencing of Human Pancreatic Cancer
Study
phs003751
-
DNA methylation dynamics during early human development
Study
JGAS000006
-
A capture methyl-seq protocol with improved efficiency and cost-effectiveness using pre-pooling and enzymatic conversion
Study
JGAS000605
-
Controlling cell differentiation with precision through understanding the structure and dynamics of gene regulatory networks
Study
JGAS000121
-
Genomics characterization of primary central nervous system lymphoma
Study
JGAS000021
-
Mutational anysis of breast cancer stem cells
Study
JGAS000304
-
DEPArray-based sorting of pure carcinoma and stromal populations from formalin-fixed paraffin-embedded (FFPE) tissues followed by shallow whole genome sequencing
Study
EGAS50000001328
-
Co-culture experiment (hashed samples)
Study
EGAS50000001252
-
APOL1 Risk Variants Induce Metabolic Reprogramming of Podocytes in Patient-Derived Kidney Organoids
Study
EGAS50000001223
-
Frequent mutations in chromatin-remodelling genes in pulmonary carcinoids
Study
EGAS00001000650
-
An oncogenic enhancer-rearrangement causes concomitant deregulation of EVI1 and GATA2 in leukemia. Targeted resequencing of chromosomal regions centered on 3q21 and 3q26 in conjunction with RNA-Seq from Acute Myeloid Leukemia patients.
Study
EGAS00001000669
-
Measuring the level of relatedness between NGS datasets
Study
EGAS00001000600
-
Reconstructing the dispersals and adaptive history of Bantu-speaking populations in Africa and North America
Study
EGAS00001002078
-
The impact of mutational clonality in predicting the response to anti-PD-L1/PD-L1 in advanced urothelial cancer
Study
EGAS00001007086
-
Tracing the origins of relapse in AML to stem cells
Study
EGAS00001002225
-
RNA stability controlled by m6A methylation contributes to X-to-autosome dosage compensation in mammals
Study
EGAS00001007112
-
Anaplastic oligodendroglioma exome and RNA sequencing data
Study
EGAS00001001209
-
Analysis of a cohort of familial ademomatous polyposis patients bearing APC gene mutation
Study
EGAS00001007237
-
H3K27ac ChIP-seq in TMPRSS2:ERG positive and negative prostate cancer tissue samples
Study
EGAS00001002496
-
Exome sequencing data from two myelosarcomas
Study
EGAS00001002562
-
Genomic and transcriptional landscape of P2RY8-CRLF2-positive childhood acute lymphoblastic leukemia
Study
EGAS00001001847
-
Analysis of the co-occurrence of LOY and CHIP in Alzheimer's disease patients and control individuals using whole-exome sequencing (WES)
Study
EGAS00001008234
-
Pangenomic classification of pituitary adenomas
Study
EGAS00001003642
-
Germline MBD4 Mutations and Predisposition to Uveal Melanoma
Study
EGAS00001003941
-
Molecular and Clonal Evolution in Recurrent Metastatic Gliosarcoma
Study
EGAS00001004076
-
Heterogeneous Genomic Evolution and Immune Microenvironments in Metastatic Lung Cancer
Study
EGAS00001004228
-
Functional_genomics_approaches_to_understand_osteoarthritis
Study
EGAS00001002322
-
Investigate the evolutionary trajectories during invasiveness acquisition in early lung adenocarcinoma
Study
EGAS00001004754
-
Genomic_profiling_of_B_other_Adult_ALL_WGS
Study
EGAS00001002474
-
Functional_genomics_approaches_to_understand_osteoarthritis
Study
EGAS00001002255
-
Investigation_of_mutational_signatures_associated_with_DNMT3A_deficiency_
Study
EGAS00001002329
-
Patient-derived organoids model treatment response of metastatic gastrointestinal cancers (targeted and whole-genome sequencing)
Study
EGAS00001002784
-
BLUEPRINT ChIP-seq data for cells in the haematopoietic lineages, from adult and cord blood samples.
Study
EGAS00001000326
-
The Simons Genome Diversity Project: 300 genomes from 142 diverse populations
Study
EGAS00001001959
-
Sequencing of pancreatic cancer primary tumors and metastases
Study
EGAS00001002186
-
Exome Sequencing in Moebius Syndrome
Study
EGAS00001001250
-
Validation_of_a_Haloplex_platform_for_targeted_re_sequencing_of_the_exons_of_25_genes
Study
EGAS00001000285
-
Screening_for_human_epigenetic_variation_at_CpG_islands
Study
EGAS00001000074
-
CRLF2_sequencing_project_
Study
EGAS00001000080
-
Detection and localization of surgically resectable cancers with a multi-analyte blood test
Study
EGAS00001002764
-
Transcriptome sequencing of Gingivo-buccal Cancer : ICGC-India Project_YR03
Study
EGAS00001002851
-
Methylation CYLD cutaneous syndrome
Study
EGAS00001003800
-
H3Africa Chip Design - Aim of designing a cost-effective GWAS chip with content appropriate for use in genomics studies of individuals from the African continent.
Study
EGAS00001002976
-
MuTHER_adipose_tissue_small_RNA_expression
Study
EGAS00001000212
-
A Unifying Paradigm for Transcriptional Heterogeneity and Squamous Features in Pancreatic Ductal Adenocarcinoma
Study
EGAS00001003974
-
Comparison_of_transcriptional_response_of_induced_pluripotent_stem__iPS__cell_derived_and_monocyte_derived_macrophages_to_bacterial_lipopolysaccharide_stimulation
Study
EGAS00001000563
-
Acquisition_of_additional_mutations_drives_accelerated_progression_of_NPM1_positive_CMML_to_AML_
Study
EGAS00001000619
-
Network-based systems pharmacology identifies heterogeneity in LCK and BCL2 signaling and differential vulnerability of T-cell acute lymphoblastic leukemia to targeted therapy
Study
EGAS00001004700
-
Spatial and temporal diversity in genomic instability processes define early stage lung cancer evolution.
Study
EGAS00001000840
-
Genetic makeup of agnospheres
Study
EGAS00001004868
-
mRNA and T cell receptor sequencing of patients with Pandemrix-associated narcolepsy type 1
Study
EGAS00001004886
-
CRLF2_sequencing_project_Exomes
Study
EGAS00001000081
-
High coverage target resequencing of coding and regulatory regions of 38 Parkinson disease genes associated either to the Mendelian or the sporadic forms of the disease
Study
EGAS00001000973
-
Spatial heterogeneity in medulloblastoma
Study
EGAS00001001014
-
Capture Hi-C identifies the chromatin interactome of colorectal cancer risk loci
Study
EGAS00001001085
-
Identification of four new susceptibility loci for testicular germ cell tumour, including variants near GAB2, GSPT1 and ZFPM1
Study
EGAS00001001302
-
DNA methylation and somatic mutations converge on cell cycle and define similar evolutionary histories in brain tumors
Study
EGAS00001001255
-
Detection of low-frequency DNA variants by targeted sequencing of the Watson and Crick strands
Study
EGAS00001005048
-
Transcriptional_Consequences_of_Copy_Number_Changes_MY_HDBR_200531
Study
EGAS00001005100
-
Targeted sequencing of 12 genes in patients with HLH
Study
EGAS00001001605
-
Recapitulation of genetic predisposition to medulloblastoma in human neuroepithelial stem cells
Study
EGAS00001003620
-
BLUEPRINT DNA Methylation 450K data of mantle cell lymphoma
Study
EGAS00001001637
-
Drugging the catalytically inactive state of RET kinase in RET-rearranged tumors.
Study
EGAS00001002335
-
Integrative genomic analyses reveal androgen-driven somatic alteration landscape in early-onset prostate cancer
Study
EGAS00001000400
-
Cancer and germline exomes consisting of FASTQ paired-end reads from melanoma and lung cancer samples
Study
EGAS00001003723
-
RNA-seq consisting of FASTQ paired-end reads from cancer samples
Study
EGAS00001003724
-
Integrative sequencing reveals alterations in untreated and castration resistant prostate cancer
Study
EGAS00001000526