-
Mutational bias in spermatogonia impacts the anatomy of regulatory sites in the human genome
Study
EGAS00001005366
-
Patient-derived neuroblastoma model system OHC-NB1
Study
EGAS00001003031
-
Germline biallelic mutation affecting the transcription factor Helios causes pleiotropic defects of immunity
Study
EGAS00001005675
-
A Single-cell Atlas of Progressive TKI Resistance in Chronic Myeloid Leukemia
Study
EGAS00001005509
-
Clonal relationships of ductal carcinoma in situ and recurrent invasive breast cancers defined by genomic analysis
Study
EGAS00001005784
-
De novo assembly of 150 Danish genomes reveals rich structural complexity
Study
EGAS00001002108
-
Clonal Decomposition and DNA Replication States Defined by Scaled Single-Cell Genome Sequencing
Study
EGAS00001003190
-
B cell receptor repertoire kinetics after SARS-CoV-2 infection and vaccination
Study
EGAS00001005816
-
Target gene sequencing for human normal endometrial glands
Study
EGAS00001005914
-
Identification of Germline Monoallelic Mutations in IKZF2 in Patients with Immune Dysregulation.
Study
EGAS00001005874
-
Changes in alternative splicing and associated neo-antigens due to therapy
Study
EGAS00001004524
-
Patient-tailored design for selective co-inhibition of leukemic cell subpopulations
Study
EGAS00001004614
-
Allele-specific expression of GATA2 due to epigenetic dysregulation in double mutated CEBPA AML
Study
EGAS00001004684
-
Genomics-based personalized oncology in cancer of unknown primary (CUP, project H021)
Study
EGAS00001004786
-
Accurate detection of tumor-specific fusion genes reveals strongly immunogenic personal neo-antigens
Study
EGAS00001004877
-
Heat selection enables highly scalable methylome profiling in cell-free DNA for noninvasive monitoring of cancer patients
Study
EGAS00001006198
-
Clonal somatic copy number altered driver events inform drug sensitivity in high-grade serous ovarian cancer
Study
EGAS00001006200
-
MutWP4__CRUK_Grand_Challenge_Mutographs_of_Cancer__Pancreatic_Organoids
Study
EGAS00001003520
-
MGP Panel: a comprehensive targeted genomics panel for molecular profiling of multiple myeloma patients
Study
EGAS00001006222
-
Discovery of a highly widespread bacteriophage family and its associations to metabolic syndrome gut microbiomes
Study
EGAS00001006260
-
Clonal relationships of ductal carcinoma in situ and recurrent invasive breast cancers defined by genomic analysis
Study
EGAS00001006306
-
Pharmacogenomic analysis of patient-derived tumor cells in gynecologic cancers
Study
EGAS00001003556
-
Treatment-mediated selection of lethal prostate cancer clones defined by copy number architectures
Study
EGAS00001006598
-
DNA methylation landscape of prostate cancer
Study
EGAS00001006670
-
Pre-neoplastic liver colonization by 11p15.5 altered mosaic cells in young children with hepatoblastoma
Study
EGAS00001006692
-
Targeted therapy of advanced parathyroid carcinoma guided by genomic and transcriptomic profiling (hipo_021)
Study
EGAS00001006747
-
Case Report: Rare IKZF1 gene fusions identified in neonate with congenital KMT2A-rearranged Acute Lymphoblastic Leukemia
Study
EGAS00001006947
-
HLA-DR is absent in primitive macrophages through epigenetic silencing of master regulator CIITA
Study
EGAS00001006981
-
RNAseq
Study
EGAS00001007165
-
Single-cell profiling of co-cultures of GSCCs and macrophages
Study
EGAS00001007482
-
Massively parallel functional dissection of schizophrenia associated non-coding genetic variants
Study
EGAS00001007542
-
Immune and clinicopathological features predict HER2-positive breast cancer prognosis in the neoadjuvant NeoALTTO and CALGB 40601 trials
Study
EGAS00001007563
-
Discovery of immunotherapy targets for pediatric solid and brain tumors by exon-level expression
Study
EGAS00001007766
-
M116 Proteome Extracellular Vesicle Profiling
Dataset
EGAD50000001679
-
Genome Diversity in Africa Project: Benin (2021-02-16)
Dataset
EGAD00001006970
-
Genome‐wide postnatal changes in immunity following fetal inflammatory response
Study
EGAS00001003635
-
Pan-neuroblastoma analysis reveals age- and signature-associated driver alterations
Study
EGAS00001003931
-
SINGLE-CELL RNA SEQUENCING Single-cell RNA sequencing was performed on 13 ‘mild-moderate’ and 10 ‘critical’ COVID19 PBMC samples
Study
EGAS00001005039
-
RNA-sequencing of tumors from 45 patients with recurrent or metastatic gastric cancer treated with immune checkpoint inhibitors
Study
EGAS00001005588
-
HTAN MCL Pre-Cancer Atlas Pilot Project - Targeted Sequencing Development Study
Study
phs002225
-
Resource for Genetic Epidemiology Research on Adult Health and Aging (GERA)
Study
phs000674
-
The Vaginal Microbiome: Disease, Genetics and the Environment
Study
phs000256
-
Human Microbiome Project Demonstration Study of Cutaneous Microbiome in Psoriasis
Study
phs000251
-
Genome Variation among HIV-Resistant People with Hemophilia
Study
phs000445
-
Analysis of the Whole Transcriptomes of Human Testis with Complete Spermatogenesis and of Human Testes with Sertoli Cell-Only Syndrome
Study
phs001777
-
Whole Transcriptome Sequencing of Human Tumor Cells and Hematopoietic Stem and Progenitor Cells During Aging and Bone Marrow Disorders
Study
phs002291
-
Germ Cell and Associated Heme Malignancies Evolve from a Common Shared Precursor
Study
phs002231
-
TNF-induced dynamic regulation of mRNA stabilome in rheumatoid arthritis fibroblast-like synoviocytes
Study
phs001371
-
Identification and Targeting of Inflammatory Macrophage-Fibroblast Crosstalk in Rheumatoid Arthritis
Study
phs001340
-
Genomic Sequencing of Cervical Cancers
Study
phs000600
-
Single Cell and Tissue Level Functional Genomics Analysis of Astrocyte-Related Mechanisms in Taupathy
Study
phs002197
-
Whole genome sequencing of core-binding factor leukemia
Study
phs000414
-
International Multi-Center ADHD Genetics Project
Study
phs000016
-
Cross-Species Single-Cell Analysis of Pancreatic Ductal Adenocarcinoma Reveals Antigen-Presenting Cancer-Associated Fibroblasts
Study
phs001840
-
Integrated Genomic Analysis of Periampullary Tumors at The Human Genome Sequencing Center, Baylor College of Medicine (HGSC-BCM)
Study
phs000895
-
Trisomy21: Risk Factors for Chromosome Nondisjunction (T21NDJ)
Study
phs000718
-
NIDDK IBD Genetics Consortium Repository Immunochip
Study
phs001721
-
Germline hypomorphic CARD11 mutations in severe atopic disease
Study
phs001369
-
Discovery of Non-ETS Gene Fusions in Human Prostate Cancer using Next Generation RNA Sequencing
Study
phs000310
-
Somatic Mutation Profile by Next Generation Sequencing in HER2+ Breast Cancer
Study
phs000770
-
Targeted MitoExome Sequencing of Mitochondrial OXPHOS Diseases (Massachusetts General Hospital)
Study
phs000339
-
Rapid Evolution of a Skin Lightening Allele in Southern African KhoeSan
Study
phs001753
-
Generation of a Cellular Atlas of Human Adipose Tissue
Study
phs002766
-
A Chromatin Accessibility Atlas of the Developing Human Telencephalon
Study
phs002033
-
Joint-Specific TF Regulation in RA
Study
phs003633
-
Tumor detection by analysis of both symmetric- and hemi-methylation of plasma cell-free DNA
Study
phs003462
-
Melanoma Genome Sequencing Project
Study
phs000452
-
Childhood Cancer Data Initiative (CCDI): Pediatric In Vivo Testing Program –Sarcoma, Kidney, and Liver Cancers
Study
phs003160
-
National Cancer Institute (NCI) Early Onset Malignancies Initiative (EOMI): Molecular profiling of Breast, Colon, Kidney, Liver, Multiple Myeloma, and Prostate among Racially and Ethnically Diverse Populations
Study
phs001952
-
Single-Cell Genomic and Transcriptomic Analysis of the Aging Human Brain
Study
phs003445
-
Examination of Engineered LINE-1 Integration Events in HeLa Cells
Study
phs001669
-
Transcriptome sequencing of human colon organoid after co-cultivation with Bifidobacterium longum
Study
JGAS000740
-
Bruno et al.: Interferon gamma rebalances immunopathological signatures in Chronic Granulomatous Disease through metabolic rewiring
Study
EGAS00001005463
-
Comprehensive gene analysis of colorectal cancer cases
Study
JGAS000128
-
Rapid detection of expanded short tandem repeats in personal genomics using hybrid sequencing.
Study
JGAS000002
-
BHD-associated kidney cancer
Study
JGAS000115
-
Genomic and Genetic Analysis of Brain Tumors and Analysis of Their Clinicopathological Significance
Study
JGAS000004
-
The impact of CCR8+ regulatory T cells on cytotoxic T cell function in human lung cancer
Study
JGAS000454
-
Microbiomic and immunogenic biomarkers of adjuvant chemotherapy efficacy in stage III colorectal cancer
Study
JGAS000875
-
Shedding light over COVID-19 susceptibility and severity
Blog
covid-19-susceptibility-and-severity
-
Recurrent somatic JAK-STAT mutations within a novel RUNX1-mutated pedigree
Study
EGAS00001001862
-
Comparison of EGF and PDGF driven glioblastomas.
Study
EGAS00001001900
-
The Genomic Landscape of Childhood and Adolescent Melanoma
Study
EGAS00001000901
-
LySeqST: A targeted sequencing assay for robust genomic classification of diffuse large B-cell lymphoma
Study
EGAS50000001601
-
The evolutionary steps from primary to metastatic prostate cancer are largely uncharted, and the ability to use DNA present in body fluids as correlates of aggregate metastatic status is under-examined. We reconstructed phylogenies in ten prostate cancer patients with fatal disease using deep targeted sequencing of the prostate, adjacent and distant organs, as well as plasma, serum, and cerebrospinal fluid at various time points. A total of 163 samples are studied.
Study
EGAS00001003848
-
Pancreatic, Small-intestinal and Pulmonary Neuroendocrine Tumors
Study
EGAS00001004878
-
Emergence of oncofetal plasticity is ubiquitous in early colorectal cancers
Study
EGAS50000001532
-
Sclerosing epithelioid fibrosarcoma case report
Study
EGAS00001005214
-
Hematopoietic Tet2 inactivation enhances the response to checkpoint blockade immunotherapy
Study
EGAS50000001191
-
IDENTIFICATION AND TARGETED MANAGEMENT OF A PATIENT WITH A NEURODEGENERATIVE DISORDER CAUSED BY BIALLELIC MUTATIONS IN SLC5A6
Study
EGAS00001003861
-
Patient-derived pediatric brain tumor organoids faithfully recapitulate primary tumors
Study
EGAS00001008305
-
Characterizing microbiome-directed fibre snacks in gnotobiotic mice and humans
Study
EGAS00001005268
-
Tumor-derived exosomes modulate PD-L1 expression in monocytes
Study
EGAS00001002377
-
The Spatial Heterogeneity in Multiple Myeloma - from the Subclonal Architecture to the Immune Microenvironment (partly hipo_K08K)
Study
EGAS00001006090
-
UK10K NEURO ABERDEEN
Study
EGAS00001000109
-
Ethiopia_Genome_Project__high_coverage_
Study
EGAS00001000237
-
Exome_trios_in_patients_with_gastroschisis
Study
EGAS00001002664
-
Allele Balance Bias Identifies Systematic Genotyping Errors and False Disease Associations
Study
EGAS00001003027
-
Exome sequencing identifies mutation of the ribosome in T-cell acute lymphoblastic leukemia
Study
EGAS00001000296
-
The Genomic Landscape of Core-Binding Factor Acute Myeloid Leukemias
Study
EGAS00001000349