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WES in HCCOs with varying Doxorubicin resistance
Study
EGAS50000000043
-
Systemic Inflammation and Lymphocyte Activation Precede Rheumatoid Arthritis
Study
phs003944
-
Exome-seq, RNA-Seq, SNP array profiling of gastric tumor samples and cell lines.
Study
EGAS00001000736
-
Recursive splicing in long vertebrate genes
Study
EGAS00001001170
-
An essential role for MYB in driving oncogenic EVI1 expression in enhancer-rearranged leukemias
Study
EGAS00001004839
-
An Isogenic Cell Line Panel for Sequence-based Screening of Targeted Anti-cancer Drugs
Study
EGAS00001005974
-
Genomic analysis and evolutionary modeling of breast and larynx cancer, based on specimens from Polish population
Study
EGAS00001006456
-
Epigenetic and metabolomic data from type 2 diabetes adolescents
Study
EGAS00001003816
-
Cergentis FFPE-TLC sequencing of colorectal carcinoma
Dataset
EGAD50000000618
-
Cookies
Documentation
cookies
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Whole Exome Sequencing in Alopecia Areata Identifies Rare Mutations in KRT82
Study
phs002632
-
Genetic Underpinnings of Ethnic Disparities in Bone Toxicities Between Hispanic and Non-Hispanic Children Treated for Acute Lymphoblastic Leukemia
Study
phs002317
-
Genetic coupling of enhancer activity and connectivity in gene expression control
Study
EGAS50000000756
-
Reference Exome Data for a Northern Brazilian population
Study
EGAS00001004112
-
Onco-exaptation of an Endogenous Retroviral LTR Drives IRF5 Expression in Hodgkin Lymphoma
Study
EGAS00001001205
-
Treatment-mediated selection of lethal prostate cancer clones defined by copy number architectures
Study
EGAS00001006598
-
HLA-DR is absent in primitive macrophages through epigenetic silencing of master regulator CIITA
Study
EGAS00001006981
-
Investigation of mutational signatures associated with DNMT3A deficiency (2019-04-03)
Dataset
EGAD00001004889
-
16S-based fecal microbiota composition
Dataset
EGAD00001004979
-
DNA whole-exome sequencing data from patients with metastatic basal cell carcinoma
Dataset
EGAD00001008675
-
Study of Women's Health Across the Nation (SWAN) Repository
Study
phs001470
-
International Multi-Center ADHD Genetics Project
Study
phs000016
-
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
-
Precision Medicine for Dilated Cardiomyopathy in European and African Ancestry
Study
phs002641
-
Joint-Specific TF Regulation in RA
Study
phs003633
-
NHLBI TOPMed - NHGRI CCDG: Pakistan Risk of Myocardial Infarction Study (PROMIS)
Study
phs001569
-
Examination of Engineered LINE-1 Integration Events in HeLa Cells
Study
phs001669
-
Rapid detection of expanded short tandem repeats in personal genomics using hybrid sequencing.
Study
JGAS000002
-
Quantitative analysis of a novel DNA hypermethylation panel for lung cancer diagnosis using bronchial specimens
Study
EGAS00001007089
-
Inhibiton of the GABPB1L-containing GABP tetramer is sufficient to reverse replicative immortality in TERT promoter mutant glioblastoma cells.
Study
EGAS00001002582
-
Mutational Patterns in Metastatic Cutaneous Squamous Cell Carcinoma
Study
EGAS00001003370
-
A somatic reference standard for cancer genome sequencing with COLO829
Study
EGAS00001001385
-
The Spatial Heterogeneity in Multiple Myeloma - from the Subclonal Architecture to the Immune Microenvironment (partly hipo_K08K)
Study
EGAS00001006090
-
RNA sequencing on colonic biopsies from inflammatory bowel disease patients treated with vehicle control, MEK inhibitor, or infliximab
Dataset
EGAD00001011333
-
Oncogenic Ectodomain deletion of FGFR1 caused by Breakage-Fusion-Bridges in Squamous Cell lung Cancer
Study
EGAS00001005059
-
3/7 Psychiatric Genomics Consortium: Finding Actionable Variation
Study
phs003138
-
Ischemic Stroke Genetics Study (ISGS)
Study
phs000102
-
The Gene Partnership (TGP) - eMERGE Data
Study
phs000495
-
Alzheimer's Disease Genetics Consortium (ADGC) Genome Wide Association Study -NIA Alzheimer's Disease Centers Cohort
Study
phs000372
-
Structural variant analysis of homologous recombination-deficient genomes
Study
EGAS00001007186
-
Analysis_of_genomic_integrity_of_disease_corrected_human_induced_pluripotent_stem_cells_by_exome_sequencing
Study
EGAS00001000055
-
Evolutionary origin and methylation status of human intronic CpG islands that are not present in mouse
Study
EGAS00001000719
-
Whole exome sequencing of an invasive diffuse intrinsic pontine glioma sampled from different sites
Study
EGAS00001002326
-
Integration of genomics and histology reveals diagnosis and effective therapy of refractory cancer of unknown primary with PDL1 amplification (H021)
Study
EGAS00001001846
-
Copy number profiling of putative cancer stem from pleural effusion aspirates from breast cancer patients
Study
EGAS00001002343
-
Defining the metastasome in colorectal cancer: Implications for hypotheses on metastasis evolution and personalized therapy (HIPO-032)
Study
EGAS00001002717
-
Conserved features of TERT promoter duplications reveal an activation mechanism that mimics hotspot mutations in cancer
Study
EGAS00001006118
-
RNA-sequencing from duodenal bipsies of Celiac disease patients
Dataset
EGAD50000000491
-
Partner independent fusion gene detection by multiplexed CRISPR Cas9 enrichment and long read Nanopore sequencing (FUDGE)
Dataset
EGAD00001006111