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Single Cell Sequencing of Sperm (scSperm)
Dataset
EGAD00001001216
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BAM files of targeted next-generation DNA sequencing data of 13 chordoid gliomas of the third ventricle
Dataset
EGAD00001003818
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Neuroblastoma cell-lines and healthy cfDNA used for the benchmarking study
Dataset
EGAD50000002199
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Transcriptome Changes in ASD (NRXN1α+/-) iPSC-derived neurons
Dataset
EGAD00001007993
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Targeted DNA sequencing on bulk bone marrow and peripheral blood
Dataset
EGAD00001011083
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Somatic mutations reveal embryonic genetic bottlenecks generating placental mosaicism
Dataset
EGAD00001006337
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Genome Denmark Phase II - alignments
Dataset
EGAD00001003157
-
Environmental Arsenic and Diabetes Mellitus (Chihuahua Cohort)
Study
phs002139
-
International Verapamil SR/Trandolapril [INVEST] Genes Study
Study
phs002319
-
Strabismus, CCDD and other anomalies
Study
phs000478
-
Molecular Evolution of Cancer
Study
phs001255
-
Intra-tumor heterogeneity and clonal evolution of papillary renal cell carcinoma
Study
phs001573
-
Center for Craniofacial and Dental Genetics: Exome Sequencing of Orofacial Cleft Families
Study
phs001675
-
Bayesian-Based Noninvasive Prenatal Diagnosis of Single-Gene Disorders
Study
phs001659
-
Pediatric Papillary Thyroid Carcinoma Whole Exome Sequencing
Study
EGAS00001005187
-
Next-Generation Sequencing of AV Nodal Reentry Tachycardia patients
Study
EGAS00001002745
-
Non-viral precision T cell receptor replacement for personalized cell therapy
Study
EGAS00001006898
-
SNP array
Dataset
EGAD00010002597
-
iPSC and iPSC derived pericytes
Dataset
EGAD50000000255
-
paired-end FASTQ files from the study: Identification of the cause of juvenile parkinsonism in a case_SYNJ1
Dataset
EGAD50000000413
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ST dataset from subcortical white matter MS lesions (CA & CI) and controls
Dataset
EGAD50000000520
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IMPRESS_all
Dataset
EGAD50000000882
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Shallow whole genome sequencing DETECT samples
Dataset
EGAD50000001333
-
APS-1 Immune Panel Sequencing
Dataset
EGAD50000000262
-
Whole Exome Sequencing of Human Gastro-esophageal Cancer PDXs
Dataset
EGAD50000001407
-
WGS data of pediatric T-ALL acute lymphoblastic leukemia (set1)
Dataset
EGAD50000002013
-
This dataset includes FASTQ for single-nucleus RNA-seq of normal controls, and multiple system atrophy (MSA) or Parkinson's disease (PD) patients.
Dataset
EGAD50000002041
-
10X single-cell Multiome (RNA+ATAC) of bone marrow-derived HSPC
Dataset
EGAD50000002326
-
Whole transcriptome and 97 antibodies of one healthy bone marrow
Dataset
EGAD00001008186
-
Single-cell RNA-seq of patient-derived organoids across three generations
Dataset
EGAD00001008431
-
WGS data subfolder HF3J5CCXY from multifocal ileal NETs study
Dataset
EGAD00001008493
-
WGS of off-target analysis of base editing in organoids
Dataset
EGAD00001009827
-
Paired WGS data of 45 samples and 2 paired WES sample of RRMM (multiple myeloma)
Dataset
EGAD00001009682
-
Whole exome sequencing (WES)
Dataset
EGAD00001011324
-
Whole genomes sequencing BAM files (blood and lung brushings) of COPD cases and controls (EvA)
Dataset
EGAD00001004535
-
Circular RNA characterization in functionally distinct brain regions
Dataset
EGAD00001004211
-
RNA-sequencing of six Pilocytic astrocytoma tumors
Dataset
EGAD00001003143
-
Bajau and Saluan adaptation study data
Dataset
EGAD00001004207
-
Single-cell Multi-omics Sequencing of Human Early Embryos
Dataset
EGAD00001004108
-
CD49f single-cell methylomes
Dataset
EGAD00001003913
-
Alcohol Dependence GWAS in European- and African Americans
Study
phs000425
-
Gene-Environment Interactions in COCCaINE Use Disorder: Collaborative Case-Control Initiative in Cocaine Addiction
Study
phs001810
-
The Genomics of Pilocytic Astrocytoma Formation in Neurofibromatosis Type 1
Study
phs000563
-
NHLBI TOPMed: Rare Variants for Hypertension in Taiwan Chinese (THRV)
Study
phs001387
-
Phenotyping and Therapeutic Approaches for Patients with Sellar/Suprasellar Disorders
Study
phs003245
-
Type 1 Diabetes Genetics Consortium (T1DGC): Case-only RNA-Seq Study
Study
phs001426
-
Epigenetic Analysis of Malnutrition
Study
phs001073
-
CADD/GADD centers on Antisocial Drug Dependence
Study
phs001841
-
Sequence Analysis of Mutations and Translocations Across Breast Cancer Subtypes
Study
phs000369
-
National Institute of Mental Health (NIMH) Amish Mennonite Bipolar Genetics Study (AmBiGen)
Study
phs000899