-
Non-invasive prenatal diagnosis by genome-wide haplotyping of maternal cell-free plasma DNA
Study
EGAS00001003634
-
ICGC Oesophageal adenocarcinoma - lymph-node samples
Study
EGAS00001000727
-
Whole transcriptome sequencing of chemotherapy-resistant muscle-invasive urothelial bladder cancer
Study
EGAS00001004232
-
Comprehensive genomic profiling of matched glioblastoma tumours, cell-lines, and xenografts reveals genomic stability and adaptation to disparate growth environments
Study
EGAS00001002709
-
Ibrutinib induces a global chromatin reorganisation in chronic lymphocytic leukaemia
Study
EGAS00001002827
-
Genetic landscape of pediatric Infant Acute Lymphoblastic leukemia
Study
EGAS00001000246
-
Fetal hemoglobin in sickle cell disease patients from Tanzania
Study
EGAS00001000990
-
Breast Cancer - Subtype defined by an amplification of the HER2 gene
Study
EGAS00001001431
-
Whole Genome Sequencing of 317 individuals from the Pacific region
Study
EGAS00001004540
-
Single-cell DNA sequencing on Pediatric MDS
Study
EGAS00001005433
-
Multiple Tissue Monitoring in Huntington disease - RNAseq skeletal muscle
Study
EGAS00001006474
-
NOTCH-mutations drive immune-escape mechanisms in B cell malignancies
Study
EGAS00001005793
-
Multiple Tissue Monitoring in Huntington disease - RNAseq fibroblasts
Study
EGAS00001006472
-
Multiple Tissue Monitoring in Huntington disease - RNAseq adipose tissue
Study
EGAS00001006473
-
Single-cell proteogenomics of MDS upon AZA
Study
EGAS00001007427
-
Single-cell genome-wide concurrent haplotyping and copy-number profiling through genotyping-by-sequencing
Dataset
EGAD00001007794
-
BLUEPRINT: Epigenetic programming during monocyte to macrophage differentiation and trained innate immunity
Dataset
EGAD00001001011
-
Preferential infiltration of distinct Vγ9δ2 T cells into Glioblastoma multiforme
Study
EGAS00001002790
-
Long-Term Outcome in Offspring and Mothers of Dexamethasone-Treated Pregnancies at Risk for Classical Congenital Adrenal Hyperplasia Owing to 21-Hydroxylase Deficiency
Study
phs001317
-
Ongoing Replication Stress Tolerance and Clonal T Cell Responses Distinguish Liver and Lung Recurrence and Patient Outcomes in Pancreatic Ductal Adenocarcinoma
Study
phs003597
-
Exome sequencing reveals pathogenic variants in known and novel candidate genes for severe sperm motility disorders
Study
EGAS00001005018
-
Autosomal recessive CD70 deficiency is associated with combined immunodeficiency and EBV viremia
Study
phs001245
-
Investigation of MMBIR DNA Repair in Normal and Cancer Human Cells
Study
phs002237
-
RNA-Seq Data From Early Stage Triple Negative Breast Cancer Tumors Treated With TVEC and Chemotherapy (MCC18621)
Study
phs003199
-
Genome Wide Association Study of Serum Creatinine during Vancomycin Therapy and Vancomycin Pharmacokinetics
Study
phs000894
-
Division of Cancer Epidemiology and Genetics (DCEG) Imputation Reference Dataset
Study
phs000396
-
Lobular Carcinomas In Situ Display Intra-Lesion Genetic Heterogeneity and Clonal Evolution in the Progression to Invasive Disease
Study
phs001006
-
Enhancer signatures stratify and predict outcomes of non-functional pancreatic neuroendocrine tumors
Study
phs001910
-
Neutralizing Antibodies against West Nile Virus Identified Directly from Human B Cells by Single-Cell Analysis and Next Generation Sequencing
Study
phs001200
-
Developing Biomarkers Incorporating High Throughput RNA, DNA, Small RNA Sequencing and Protein Expression in Inflammatory Bowel Disease Using Formalin-Fixed, Paraffin-Embedded (FFPE) Tissue Samples
Study
phs003156
-
MATISSE Whole-exome sequencing data
Dataset
EGAD50000001469
-
Transcriptomic profiling of proximal and distal regions of human long head biceps tendon
Study
EGAS50000001454
-
Human data for chromatin accessibility (ATAC-Seq and scATAC-Seq) and transcriptome (RNA-Seq and scRNA-Seq) in eight B-cell precursors, from HSC to Naive B cells
Study
EGAS00001007296
-
Interplay of somatic alterations and immune infiltration modulates response to PD-1 blockade in advanced clear cell renal cell carcinoma -- CA209-010
Dataset
EGAD00001006026
-
Interplay of somatic alterations and immune infiltration modulates response to PD-1 blockade in advanced clear cell renal cell carcinoma -- CA209-025
Dataset
EGAD00001006029
-
Somatic mutation rates scale with lifespan across mammals
Dataset
EGAD00001008032
-
Targeted de novo phasing and long-range assembly by template mutagenesis
Dataset
EGAD00001008444
-
Common early-life exposure of the colorectal epithelium to the microbiome-derived mutagen colibactin
Dataset
EGAD00001015830
-
Interplay of somatic alterations and immune infiltration modulates response to PD-1 blockade in advanced clear cell renal cell carcinoma -- CA209-009
Dataset
EGAD00001006027
-
Characterization of mutational signatures in human cancer cell lines reveals episodic APOBEC mutagenesis
Dataset
EGAD00001004201
-
DNA Double Strand Breaks in KMT2A-Rearranged AML patients
Study
phs002804
-
Genome Sequencing of Hepatocellular Carcinoma at The Human Genome Sequencing Center of Baylor College of Medicine (HGSC-BCM)
Study
phs000509
-
Rapid Acceleration of Diagnostics - Digital Health Technologies (RADx-DHT): Large Scale Flu Surveillance Study (LSFS)
Study
phs002539
-
NHLBI TOPMed: Australian Familial Atrial Fibrillation Study
Study
phs001435
-
Targeted Sequencing of Primary ER-positive Breast Tumors Treated with 5 Years of Tamoxifen
Study
phs001234
-
The Finland-United States Investigation of NIDDM Genetics (FUSION) Study
Study
phs000100
-
GWAS for IgA Nephropathy
Study
phs000431
-
Dysregulation of Naive T Cell Quiescence during Aging
Study
phs003400
-
10x genomics single cell RNA-seq and ATAC-seq from 10 pre-menopausal patients fimbriae and ampullary part of the fallopian tube
Study
EGAS50000000628
-
NHLBI TOPMed - NHGRI CCDG: Intermountain INSPIRE Registry
Study
phs001545