-
Structural Alterations Driving Castration-Resistant Prostate Cancer Revealed by Linked-Read Genome Sequencing
Study
phs001577
-
To reveal the spectrum of gene mutations in grade II/III gliomas, whole exome sequencing of 52 samples including 4 multi-regional and 10 multi-time points sampling cases and 293 SNP-array were performed.
Study
EGAS00001001045
-
RNA-seq of oropharynx cancer cases from University of Michigan
Dataset
EGAD50000001306
-
Functional Dynamics of the Elderly Gut Microbiome During Probiotic Consumption
Study
phs000896
-
Structure of the Mucosal and Stool Microbiome in Lynch Syndrome
Study
phs002343
-
PD-1 antibody-bound progenitor-exhausted CD8+ T cells in lymph nodes boost PD-1-blockade anti-tumor immunity in gastrointestinal cancer
Study
JGAS000720
-
Adjuvant nivolumab in resected esophageal or gastroesophageal junction cancer: exploratory biomarker analyses from CheckMate 577
Study
EGAS50000001663
-
MGA-NUTM1 fusion in high grade spindle cell sarcoma
Study
EGAS00001003341
-
Inferring expressed genes by whole-genome sequencing of plasma DNA
Study
EGAS00001001754
-
Dynamics of neoantigen landscape during immunotherapy
Study
EGAS00001002704
-
Comparative analysis of somatic variant calling on matched FF and FFPE WGS samples
Study
EGAS00001004456
-
Latency and interval therapy affect the evolution in metastatic colorectal cancer
Study
EGAS00001003646
-
Tissue and plasma RNA from esophageal cancer and precursor lesions
Study
EGAS00001004939
-
A Single-Cell Atlas of the Multicellular Ecosystem of Primary and Metastatic Hepatocellular Carcinoma
Study
EGAS00001004468
-
High-resolution, patient-level dissection of IL-23 blockade in cutaneous psoriasis
Study
EGAS00001007373
-
RNA sequencing data for primary and recurrent ovarian granulosa cell tumors
Dataset
EGAD00001009108
-
scRNA-seq of LN and lymphoma stroma
Study
EGAS00001005732
-
Patient-Specific Factors Influence Somatic Variation Patterns in Von Hippel-Lindau Disease Renal Tumors
Study
phs001107
-
Multiregion Sequencing of Localized Prostate Cancer
Study
phs001465
-
Systematic Analysis of Transcription Program Regulation by Transcription Factor EB (TFEB)
Study
phs002099
-
Genetic_background_for_cardio_vascular_disorders_in_the_general_Finnish_population
Study
EGAS00001000229
-
Transcriptome human nasal epithelium
Dataset
EGAD00001002226
-
Targeted gene fusion sequencing (Fus-seq) in mesothelioma
Dataset
EGAD00001000361
-
Mucosal Melanoma transcriptomes
Dataset
EGAD50000000892
-
Genetic architecture of disease in Greenland is shaped by demographic history, fine-structure, and selection - WGS data
Dataset
EGAD50000000933
-
Next-generation sequencing-based comprehensive genetic analysis of undiagnosed disease
Study
JGAS000522
-
Helleday_HRAS_Project
Study
EGAS00001000332
-
Landscape and significance of multiple mutations in oncogenes.
Study
EGAS00001003763
-
Whole Exome Sequencing in Alopecia Areata Identifies Rare Mutations in KRT82
Study
phs002632
-
RCC_HTA2.0_Reustle2022
Dataset
EGAD00010002352
-
Fragmentomics profiling and quantification of plasma Epstein-Barr virus DNA enhance prediction of future nasopharyngeal carcinoma.
Dataset
EGAD50000000580
-
MET amplification in gastric cancer
Dataset
EGAD50000001099
-
Identification of phenotype-modifier genes
Study
EGAS50000000829
-
Esophageal Adenocarcinoma Organoid Genomics
Study
EGAS00001005224
-
Project MinE Illumina Infinium HumanMethylation450 (450k) BeadChip data on 2,790 Dutch whole blood samples, including 1,761 ALS patients of which 119 are known carriers of the C9orf72 repeat expansion.
Study
EGAS00001004587
-
Transcriptomic signatures of CD4+ T cells from visceral leishmaniasis (VL) patients
Dataset
EGAD00001005807
-
Myeloid cancer sequencing data
Dataset
EGAD00001007791
-
Single-nucleus Isoforms of Down Syndrome Brains (long-read)
Dataset
EGAD00001008286
-
DNA methylation-based classification of sinonasal tumors [DNA sequencing]
Dataset
EGAD00001009668
-
Whole genome sequencing of HSPC and SI clones of disomy- and trisomy 21 fetuses samples (Novaseq 6000 samples)
Dataset
EGAD00001006343
-
NHLBI GO-ESP: Family Studies (Mendelian Lipid Disorders)
Study
phs000587
-
A common single nucleotide variant in T is strongly associated with chordoma
Dataset
EGAD00001000226
-
Genomic characterization of co-existing biliary tract intraepithelial neoplasia and carcinoma lesions reveals distinct evolutionary paths of gallbladder cancer
Dataset
EGAD00001007792
-
High Frequency Ventilation in Premature Infants (HIFI-BioLINCC)
Study
phs004032
-
Longitudinal Study of Fluoride and Other Factors Related to Dental Fluorosis, Dental Caries, and Bone Health
Study
phs002203
-
Ballett
Study
EGAS50000000478
-
Transcriptome and epigenomic landscape of cytotrophoblasts from normal and HDP placentas
Study
JGAS000667
-
PEVOsq
Study
EGAS50000000731
-
Metabolomic and transcriptomic analyses identify metabolic alterations and immune suppression in ovarian cancer
Study
JGAS000831
-
Regions of common inter-individual DNA methylation differences in human monocytes.
Study
EGAS00001002265
-
Next generation sequencing of sporadic schwannomatosis samples
Study
EGAS00001000767
-
Genetic landscape of relapsed DLBCL
Study
EGAS00001001553
-
Assessment_of_genetic_and_epigenetic_variation_in_human_IPS_cells
Study
EGAS00001000231
-
Celiac disease-specific intestinal T cells analyzed with HLA-class II tetramers, RNA-seq and mass cytometry have a narrow, autoimmune-associated phenotype
Study
EGAS00001003017
-
Genomic profiling of paediatric glioma cell lines
Study
EGAS00001003006
-
Assessment_of_genetic_and_epigenetic_variation_in_human_IPS_cells
Study
EGAS00001000492
-
Multiomic profiling of pleomorphic rhabdomyosarcoma
Study
EGAS00001007230
-
NIH RECOVER: A Multi-Site Observational Study of Post-Acute Sequelae of SARS-CoV-2 Infection in Adults
Study
phs003463
-
Discovery and validation of an ancillary genomic test of malignancy for primary melanocytic tumors
Study
EGAS50000000887
-
Exome sequencing of early and late passage Patient Derived Xenogratf Tumoroids with matched Patient Derived Xenogratfs and matched normal liver
Study
EGAS50000000185
-
The epigenetic landscape controlled by p63 in epidermal development
Study
phs001737
-
Location and Function of NSun2-Mediated Cytosine-5 Methylation in RNA and its Effect on Translation
Study
phs000645
-
Single-Cell Multi-Omic Analysis of the Vestibular Schwannoma Ecosystem Uncovers a Nerve Injury-Like State
Study
phs003318
-
3q-capture DNA sequencing of primary AMLs with 3q26 rearrangements
Dataset
EGAD00001006820
-
To reveal the spectrum of gene mutations in grade II/III gliomas, whole exome sequencing of 52 samples including 4 multi-regional and 10 multi-time points sampling cases and 291 SNP-array were performed.
Study
EGAS00001001044
-
Pediatric Papillary Thyroid Carcinoma RNA-Seq
Dataset
EGAD00001007499
-
Genetic Epidemiology Network of Salt Sensitivity (GenSalt)
Study
phs000784
-
Genetic architecture of disease in Greenland is shaped by demographic history, fine-structure, and selection - MEGA chip data
Dataset
EGAD50000000934
-
Repression of CADM1 transcription by HPV type 18 is mediated by three-dimensional rearrangement of promoter-enhancer interactions
Dataset
EGAD50000001135
-
Whole genome, whole exome and transcriptome sequencing of 10 ccRCC with Von Hippel-Lindau disease
Study
JGAS000544
-
Enzymatic Methyl-Seq Rectal Mucus
Study
EGAS50000001314
-
16S rRNA Rectal Mucus
Study
EGAS50000001262
-
RNA-sequencing data from metastatic Castration-Resistant Prostate Cancer (mCRPC)
Study
EGAS00001005954
-
TCR sequencing of head and neck cancers
Dataset
EGAD00001007917
-
Orphan_Tumour_Study___familial_neuroblastoma
Study
EGAS00001002171
-
scRNA sequencing of in vitro generated suppressive myeloid cells using parental and Sialidase expressing A549 cancer cell lines
Dataset
EGAD50000000351
-
WES of precancerous lesions from 10 lynch patients and 3 sporadics
Dataset
EGAD50000000644
-
Comprehensive analysis of interaction between human gene expression and environmental metagenomes.
Study
JGAS000321
-
single cell RNA-seq data of 10 small cell lung cancer patients
Dataset
EGAD50000002034
-
GATA1 scD&D-seq integrated with Multiome
Dataset
EGAD50000002299
-
Longitudinal RNA-seq (whole blood) in a twin cohort
Study
EGAS00001001763
-
Tumor HTG EdgeSeq from metastatic castrate resistant prostate cancer
Study
EGAS00001004852
-
Enhanced reduced representation bisulfite sequencing (eRRBS) on 45 multiple myeloma samples and 3 normal plasma cell
Study
EGAS00001004348
-
Colorectal cancer genomics with primary and metastatic samples
Study
EGAS00001006465
-
Colorectal cancer transcriptomics with primary and metastatic samples
Study
EGAS00001006464
-
RNA-sequencing of a normal CD34+ cells
Dataset
EGAD00001007646
-
RNA Seq of 25 spheres derived from lymph nodes of lung cancer patients
Dataset
EGAD00001011099
-
De novo mutations in cell-free foetal DNA - Pulldown experiment
Dataset
EGAD00001002265
-
Whole genome sequencing of metastatic cutaneous squamous cell carcinoma
Dataset
EGAD00001004530
-
Capture Hi-C on Hodgkin lymphoma
Dataset
EGAD00001004321
-
Sequencing data from triple-negative breast cancer tumors
Study
EGAS50000001585
-
Sequencing data from triple-negative breast cancer tumors
Study
EGAS50000001598
-
RB Loss in Resistant EGFR Mutant Lung Adenocarcinomas that Transform to Small Cell Lung Cancer
Study
EGAS00001001102
-
RNA isoform repertoire of neuropsychiatric risk genes in human brain
Study
EGAS00001007744
-
Luminal progenitor cell line iHBEC(CD117)
Dataset
EGAD50000000723
-
Unravelling the contribution of HIF pathway and its therapeutic potential in human AML leukemia-initiating cells
Dataset
EGAD00001008514
-
Dataset for upper_gastrointestinal_tumor-RNA
Dataset
EGAD00001008853
-
Dataset for Sarcoma-WES linked from study EGAS00001004813
Dataset
EGAD00001010258
-
RNA-seq and Hi-C data of a chromothripsis patient's iPS cells
Dataset
EGAD00001002242
-
Whole genome sequencing of multiple myeloma patient samples.
Dataset
EGAD00001004452