-
Genetics of Disorders Affecting Tooth Structure, Number, Morphology and Eruption
Study
phs001491
-
A Natural History Study of CMT1B, CMT2A, CMT4A and CMT4C
Study
phs001419
-
Detection and Targeting of Splicing Deregulation in Pediatric Acute Myeloid Leukemia Stem Cells
Study
phs003196
-
Performance comparison of three DNA extraction kits on human whole-exome data from formalin-fixed paraffin-embedded normal and tumor samples
Study
EGAS00001002631
-
DNA hypermethylation and differential gene expression associated with Klinefelter syndrome
Study
EGAS00001002797
-
Partner-independent fusion gene detection by multiplexed CRISPR/Cas9 enrichment and long-read Nanopore sequencing
Study
EGAS00001003964
-
Genomewide Association Study of Alcohol Use and Alcohol Use Disorder in Australian Twin-Families (OZ-ALC GWAS)
Study
phs000181
-
The NCAA-DoD Concussion Assessment, Research, and Education (CARE) Consortium
Study
phs002175
-
Acute Respiratory Distress Network (ARDSNet) Study 04 Assessment of Low Tidal Volume and Elevated End-Expiratory Volume to Obviate Lung Injury (ALVEOLI-BioLINCC)
Study
phs003714
-
A Joint Linkage/Association Strategy to Interrogate AMD Genetic Susceptibility
Study
phs001379
-
Genomic Characterization of Patient-Derived Xenograft Models to Improve Targeted Therapy for HER2+ Breast Cancer Brain Metastases Treatments
Study
phs001063
-
Novel Factors for Unexplained Phenotypes of Subclinical Carotid Atherosclerosis
Study
phs001560
-
Multiregion Sequencing of Localized Prostate Cancer
Study
phs001465
-
OCD Collaborative Genetic Association Study (OCGAS)
Study
phs000903
-
Single Cell Analysis of Sporadic Human Basal Cell Carcinomas
Study
phs003103
-
FinaleMe: Predicting DNA Methylation by the Fragmentation Patterns of Plasma Cell-Free DNA
Study
phs003287
-
Circulating RNAs in Acute Heart Failure (CRUCIAL)
Study
phs003403
-
NHLBI TOPMed - NHGRI CCDG: Groningen Genetics of Atrial Fibrillation (GGAF) Study
Study
phs001725
-
Japanese Reference Genome JG1
Study
JGAS000259
-
SCI-MAP: Single Cell Microgel embedded iPS-cells to map molecular variability of cell differentiation using a systems biology approach.
Study
EGAS50000001041
-
Whole-Genome Shotgun Metagenomic Analysis of Rectal Mucus for Colorectal Cancer Detection
Study
EGAS50000001310
-
NOUS-209 off-the-shelf immunotherapy has the potential to hit primary and metachronous colorectal and urothelial cancer in Lynch syndrome
Study
EGAS50000001336
-
B cell activation
Study
EGAS50000001468
-
Mechanism of Decitabine response in MDS/AML patients
Study
EGAS50000000924
-
Primary plasma cell leukemia (pPCL) samples were sequenced using the Nimblegen MedExome hybridization capture to detect translocations, copy number changes, and mutations in 20 pPCL samples and patient matched controls.
Study
EGAS00001003104
-
Methylation_changes_in_OA_patients_with_chronic_exposure_to_cobalt_and_chromium
Study
EGAS00001001180
-
Whole genome sequencing data of paediatric KMT2A-rearranged acute lymphoblastic leukemia
Study
EGAS50000001079
-
The exomic landscape of t(14,18) negative diffuse follicular lymphoma with 1p36 deletion
Study
EGAS00001002594
-
ATACseq - Notch Signaling Maintains a Progenitor-Like Subclass of Hepatocellular Carcinoma
Study
EGAS50000000516
-
Divergent WNT Signaling and Drug Sensitivity Profiles within Hepatoblastoma Tumors and Organoids
Study
EGAS50000000561
-
Unraveling metastatic progression of breast cancer
Study
EGAS00001000760
-
Alternative lengthening of telomeres in childhood neuroblastoma from genome to proteome
Study
EGAS00001004349
-
Indonesian Genome Diversity Project 2
Study
EGAS00001003654
-
Pathogenic Neurofibromatosis type 1 (NF1) RNA splicing resolved by targeted RNAseq
Study
EGAS00001005530
-
Understanding_hematopoietic_stem_cell_mobilization_and_engraftment_
Study
EGAS00001004620
-
Clinical utility of combined low-pass whole genome and targeted sequencing in liquid biopsies for diagnosis and monitoring of pediatric solid tumors
Study
EGAS00001006913
-
Organ_maturation_in_preparation_for_birth__Peds_RFA__to_develop_a_tissue__resource_and_a_single_cell_atlas_of_organ_development_and_maturation_for__dissemination_among_the_scientific_and_clinical_community__RNA
Study
EGAS00001008256
-
scRNA seq and scTCR seq data from 5 melanoma patients
Dataset
EGAD50000001155
-
Optimized Polyepitope Neoantigen DNA Vaccines Elicit Neoantigen-Specific Immune Responses in Preclinical Models and in Clinical Translation
Study
phs002342
-
Case Study of Acquired Resistance to FGFR Inhibition in Cholangiocarcinoma using Targeted DNA and RNA Sequencing
Study
phs001924
-
Target sequencing of a case of concurrent Langerhans Cell Histiocytosis and Acute Myeloid Leukemia
Study
JGAS000558
-
Comprehensive analyses of clinicopathological features and genomic mutations of combined hepatocellular-cholangiocarcinoma
Study
JGAS000599
-
PDAC Phenotype and Germline Genotype Data Access Committee
Dac
EGAC50000000893
-
WES of oral-mucosa-derived organoids
Dataset
EGAD00001005063
-
Transcriptional programming in whole blood reveals changes in pro-inflammatory phenotype explained by changed food and changed life style.
Dataset
EGAD00001006051
-
4_eCLIP_NOVA1_NOVA2_RBFOX2
Dataset
EGAD00001008428
-
scATAC sequencing of FACS sorted CD4+ T and CD25+ T from isolated tissues
Dataset
EGAD00001006779
-
Congenital mesoblastic nephroma and infantile fibrosarcoma
Dataset
EGAD00001003885
-
Profiling Chromatin Accessibility in Humans Using Adenine Methylation and Long-Read Sequencing
Study
EGAS00001007852
-
Whole genome sequencing, SNP array and RNA-seq of uveal melanomas
Study
EGAS00001000472
-
Methylation profiling of osteoblastomas and their mimics
Study
EGAS00001005932
-
Whole genome sequencing of HSPC and SI clones of disomy- and trisomy 21 fetuses samples (Novaseq 6000 samples)
Dataset
EGAD00001006343
-
scRNAseq dataset of myeloid cells from secondary lymphoid organs from lymphoma patients and controls
Dataset
EGAD50000001629
-
The brain neurovascular epigenome and its association with dementia
Dataset
EGAD50000001657
-
BestAgeingMiRNA
Dataset
EGAD00010002788
-
STAMPEED: Northern Finland Birth Cohort 1966 (NFBC1966)
Study
phs000276
-
Cell and Circuit-Specific Exploration of HIV Neurogenomics in Context of Opiate and Cocaine Misuse
Study
phs003080
-
Common Fund (CF) Genotype-Tissue Expression Project (GTEx)
Study
phs000424
-
Genetic Studies of Chronic Kidney Disease (CKD)
Study
phs001828
-
Effect of the Placental Transcriptome on Stunting in a Longitudinal African Cohort
Study
phs001782
-
Shanghai Breast Cancer Genetics Study (SBCGS)
Study
phs001088
-
Polycystic Ovary Syndrome (PCOS) Genetics
Study
phs000368
-
Shanghai Breast Cancer Genetics Study (SBCGS)
Study
phs000799
-
NEI CIDR Methylation Profiling of Primary Open Angle Glaucoma in GLAUGEN Samples
Study
phs000461
-
A Scalable, GMP-Compatible, Autologous Organotypic Cell Therapy for Dystrophic Epidermolysis Bullosa
Study
phs003271
-
Precision High Intensity Training Through Epigenetics (PHITE)
Study
phs003873
-
Molecular Tumor Board to Inform on Personalized Medicine for a Man with Advanced Prostate Cancer
Study
EGAS00001004648
-
The University of Hong Kong Colon Cancer GCV Study
Study
EGAS00001006707
-
One-step generation of tumor models by base editor multiplexing in adult stem cell-derived organoids
Study
EGAS00001006886
-
Rare Disease Susceptibility Variant Study in Children with Crohn's Disease and Their Parents Using Targeted Gene Sequencing.
Study
phs001751
-
Whole Exome and Transcriptome Sequencing in Sporadic ALS
Study
phs000747
-
SNPs and Extent of Atherosclerosis (SEA) Study
Study
phs000349
-
The Genomic Landscape of Endocrine Resistant Advanced Breast Cancers: Paired Pre- and Post-endocrine Therapy Samples.
Study
phs001674
-
Cholesterol and Pharmacogenetics (CAP) Study
Study
phs000481
-
A Genome-Wide Association Study on Cataract and HDL in the Personalized Medicine Research Project Cohort
Study
phs000170
-
Early Family Prevention of Adolescent Alcohol, Drug Use, and Psychopathology
Study
phs003442
-
Detecting and Subtyping Lung Cancer Through Analysis of Circulating Tumor DNA
Study
phs003570
-
HuBMAP: Single-Cell Multiplex Chromatin and RNA Interactions in Aging Human Brain
Study
phs003568
-
Development and first-in-human CAR T therapy targeting the pathognomonic MiT-fusion driven protein GPNMB
Study
EGAS50000001696
-
Functional single-cell characterization of immune aplastic anemia shows convergence of NK and NK-like CD8+ T cells with disease-associated TCR signature
Study
EGAS00001007602
-
Widespread DNA hypomethylation and differential gene expression in Turner syndrome
Study
EGAS00001002190
-
Functional single-cell characterization of immune aplastic anemia shows convergence of NK and NK-like CD8+ T cells with disease-associated TCR signature
Study
EGAS00001007604
-
Stability of gut microbiome after COVID-19 vaccination in healthy and immuno-compromised individuals
Study
EGAS50000000179
-
Distinct immune cell infiltration patterns in PDAC exhibit divergent immune cell selection and immunosuppressive mechanisms
Study
EGAS50000000726
-
Genetic coupling of enhancer activity and connectivity in gene expression control
Study
EGAS50000000756
-
The proliferative history shapes the DNA methylome of B-cell tumor and predicts clinical outcome
Study
EGAS00001004640
-
The molecular basis of T-PLL is an actionable perturbation of TCL1/ATM- and epigenetically instructed damage responses
Study
EGAS00001002744
-
H3Africa - Identification and characterization of novel hereditary neurological disease genes in Mali.
Study
EGAS00001003016
-
SINGLE-CELL RNA SEQUENCING Single-cell RNA sequencing was performed on 13 ‘mild-moderate’ and 10 ‘critical’ COVID19 PBMC samples
Study
EGAS00001005039
-
eMERGE Network Phase III: HRC SNV and 1000 Genomes SV Imputed Array Data of 105,000 Participants
Study
phs001584
-
National Heart Lung and Blood Institute (NHLBI) GO-ESP: Heart Cohorts Component of the Exome Sequencing Project (ARIC)
Study
phs000398
-
Sleep Abnormalities in Rare Genetic Disorders: Angelman Syndrome, Rett Syndrome, and Prader-Willi Syndrome
Study
phs001292
-
Kids First: Congenital Heart Defects and Laterality Birth Defects
Study
phs002589
-
National Heart Lung and Blood Institute (NHLBI) GO-ESP: Heart Cohorts Component of the Exome Sequencing Project (FHS)
Study
phs000401
-
National Heart Lung and Blood Institute (NHLBI) GO-ESP: Heart Cohorts Component of the Exome Sequencing Project (JHS)
Study
phs000402
-
Gabriella Miller Kids First Pediatric Research Program in Germline and Somatic Variants in Myeloid Malignancies in Children
Study
phs002187
-
National Heart Lung and Blood Institute (NHLBI) GO-ESP: Heart Cohorts Component of the Exome Sequencing Project (CHS)
Study
phs000400
-
MicroRNAs, Hypertension and End Organ Damage in Humans
Study
phs002389
-
Next Generation Mendelian Genetics: Familial Combined Hyperlipidemia
Study
phs000538
-
Post-liver transplant recurrent human hepatocellular carcinoma study (RHCCS)
Study
phs000782