-
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
-
The Genetic Evolution of Acral Melanoma
Study
phs003451
-
Transgenerational Transmission of Post-Zygotic Mutations Suggests Symmetric Contribution of First Two Blastomeres to Human Germline
Study
phs003781
-
Beta-Blocker Evaluation in Survival Trial (BEST-BioLINCC)
Study
phs003730
-
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
-
Prospective Investigation of Pulmonary Embolism Diagnosis (PIOPED-BioLINCC)
Study
phs004020
-
Immediate Postoperative Minimal Residual Disease Detection with MAESTRO Predicts Recurrence and Survival in Head and Neck Cancer Patients Treated with Surgery
Study
phs003981
-
P4HA1 Mediates Hypoxia-Induced Invasion in Human Pancreatic Cancer Organoids
Study
phs003961
-
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
-
The Formation and Propagation of Human Robertsonian Chromosomes
Study
phs003920
-
Childhood Cancer Data Initiative (CCDI): Molecular Characterization Initiative
Study
phs002790
-
Identification of a Type 1 Diabetes-Associated T Cell Receptor Repertoire Signature from the Human Peripheral Blood
Study
phs003979
-
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
-
Single-cell bisulfite-seq analyses of 1-year-old prospermatogonia and adult spermatogonial stem cell
Study
JGAS000887
-
Single-cell bisulfite-seq analyses of 29-year-old prospermatogonia and adult spermatogonial stem cell
Study
JGAS000888
-
Analysis of the co-occurrence of LOY and CHIP in Alzheimer's disease patients and control individuals using whole-exome sequencing (WES)
Study
EGAS00001008234
-
An ancient DNA perspective on the Russian Conquest of Yakutia
Study
EGAS50000001329
-
BLUEPRINT Hematopoietic Stem/Progenitor Cell Methylomes
Study
EGAS00001002070
-
Genetic landscape of pediatric Retinoblastoma
Study
EGAS00001000346
-
Human papillomavirus integration induces oncogenic host gene fusions in oropharyngeal cancers
Study
EGAS50000000892
-
Single-nucleus brain transcriptomics reveals microglia dysfunction in Multiple System Atrophy
Study
EGAS50000001406
-
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
-
Long-read sequencing of saliva collected and stablized at room temperature in Oragene devices on the PacBio Revio
Study
EGAS50000001666
-
Anaplastic oligodendroglioma exome and RNA sequencing data
Study
EGAS00001001209
-
A Unifying Paradigm for Transcriptional Heterogeneity and Squamous Features in Pancreatic Ductal Adenocarcinoma
Study
EGAS00001003974
-
The function of circular RMST in neuroendocrine tumours
Study
EGAS50000000897
-
A benchmark of DNA methylation deconvolution methods for tumoral fraction estimation using DecoNFlow
Study
EGAS50000001529
-
APOL1 Risk Variants Induce Metabolic Reprogramming of Podocytes in Patient-Derived Kidney Organoids
Study
EGAS50000001223
-
Reconstructing the dispersals and adaptive history of Bantu-speaking populations in Africa and North America
Study
EGAS00001002078
-
PDX_models_from_Latin_America_RNAseq
Study
EGAS00001008150
-
Genomic and transcriptional landscape of P2RY8-CRLF2-positive childhood acute lymphoblastic leukemia
Study
EGAS00001001847
-
PDX_models_from_Latin_America_WES_
Study
EGAS00001005663
-
Sequencing of pancreatic cancer primary tumors and metastases
Study
EGAS00001002186
-
Ensilication as a Cold‑Chain–Free Solution for High‑Fidelity DNA Preservation in tumor samples
Study
EGAS50000001698
-
A Comprehensive Catalogue of Somatic Mutations from a Human Cancer Genome
Study
EGAS00000000052
-
The Simons Genome Diversity Project: 300 genomes from 142 diverse populations
Study
EGAS00001001959
-
RNAseq_of_healthy_mesothelial_cells_and_primary_mesothelioma_cell_lines
Study
EGAS00001005728
-
Genomic_profiling_of_B_other_Adult_ALL_WGS
Study
EGAS00001002474
-
Measuring the level of relatedness between NGS datasets
Study
EGAS00001000600
-
CIRdb: Array genotype data
Study
EGAS00001006050
-
Massive Genomic Rearrangment Acquired in a Single Catastrophic Event During Cancer Development
Study
EGAS00000000029
-
Validation_of_a_Haloplex_platform_for_targeted_re_sequencing_of_the_exons_of_25_genes
Study
EGAS00001000285
-
Patient-derived organoids model treatment response of metastatic gastrointestinal cancers (targeted and whole-genome sequencing)
Study
EGAS00001002784
-
Molecular and Clonal Evolution in Recurrent Metastatic Gliosarcoma
Study
EGAS00001004076
-
Sequencing data from a highly cost-effective cell-free DNA methylome test
Study
EGAS00001008125
-
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
-
BCR-ABL is enriched in S- and G2-cell cycle phases
Study
EGAS00001006769
-
Identification of cis- and trans-regulatory variation modulating microRNA expression levels in human fibroblasts
Study
EGAS00000000056
-
Whole-genome sequencing across 449 samples spanning 47 ethnolinguistic groups provides insights into genetic diversity in Nigeria
Study
EGAS00001007036
-
PDX_models_from_Latin_America_RNAseq_Xenofiltered
Study
EGAS00001008232
-
PDX_models_from_Latin_America_Xenofiltered_WES
Study
EGAS00001008231
-
BLUEPRINT ChIP-seq data for cells in the haematopoietic lineages, from adult and cord blood samples.
Study
EGAS00001000326
-
Frequent mutations in chromatin-remodelling genes in pulmonary carcinoids
Study
EGAS00001000650
-
Combination_therapies_for_personalized_cancer_medicine
Study
EGAS00001000655
-
Pangenomic classification of pituitary adenomas
Study
EGAS00001003642
-
Methylation CYLD cutaneous syndrome
Study
EGAS00001003800
-
Germline MBD4 Mutations and Predisposition to Uveal Melanoma
Study
EGAS00001003941
-
TenK10K Phase 1: Single Cell
Study
EGAS50000001653
-
Heterogeneous Genomic Evolution and Immune Microenvironments in Metastatic Lung Cancer
Study
EGAS00001004228
-
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
-
Investigate the evolutionary trajectories during invasiveness acquisition in early lung adenocarcinoma
Study
EGAS00001004754
-
Tracing the origins of relapse in AML to stem cells
Study
EGAS00001002225
-
Identification of four new susceptibility loci for testicular germ cell tumour, including variants near GAB2, GSPT1 and ZFPM1
Study
EGAS00001001302
-
Functional_genomics_approaches_to_understand_osteoarthritis
Study
EGAS00001002322
-
Exome sequencing data from two myelosarcomas
Study
EGAS00001002562
-
Colorectal advanced adenomas NKI-AvL TGO COCOS series
Study
EGAS00001002952
-
Whole-genome sequencing in 14 cases and whole-exome sequencing in 90 cases of Chinese ESCC
Study
EGAS00001001487
-
Exome Sequencing in Moebius Syndrome
Study
EGAS00001001250
-
Functional_genomics_approaches_to_understand_osteoarthritis
Study
EGAS00001002255
-
Investigation_of_mutational_signatures_associated_with_DNMT3A_deficiency_
Study
EGAS00001002329
-
CRLF2_sequencing_project_
Study
EGAS00001000080
-
Screening_for_human_epigenetic_variation_at_CpG_islands
Study
EGAS00001000074
-
H3K27ac ChIP-seq in TMPRSS2:ERG positive and negative prostate cancer tissue samples
Study
EGAS00001002496
-
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
-
DEPArray-based sorting of pure carcinoma and stromal populations from formalin-fixed paraffin-embedded (FFPE) tissues followed by shallow whole genome sequencing
Study
EGAS50000001328
-
Detection and localization of surgically resectable cancers with a multi-analyte blood test
Study
EGAS00001002764
-
Evolutionary analysis of pancreatic cancer and coexistent precursor lesions using whole exome sequencing data
Study
EGAS00001002778
-
Transcriptome sequencing of Gingivo-buccal Cancer : ICGC-India Project_YR03
Study
EGAS00001002851
-
MuTHER_adipose_tissue_small_RNA_expression
Study
EGAS00001000212
-
SCANDARE MACARON
Study
EGAS50000000145
-
Co-culture experiment (hashed samples)
Study
EGAS50000001252
-
Deregulation of FOXF1/FENDRR from t(14;16)(q32;q24) defines a subtype of high risk lineage ambiguous leukemia
Study
EGAS50000001255
-
Clonally heritable gene expression imparts a layer of diversity within cell types
Study
EGAS50000000161