-
Low-pass nanopore whole genome sequencing of brain tumors
Dataset
EGAD00001003382
-
eMERGE Network's Multi-Center Pilot of Pharmacogenetic Sequencing in Clinical Practice
Study
phs000906
-
Meningioma Exome
Dataset
EGAD00001000099
-
RNA-seq of tumor samples from clear cell renal cell carcinoma patients included in the Translational Program of the NIVOREN GETUG-AFU-26 trial
Study
EGAS50000001057
-
RNA-seq after drug perturbation of primary lymphoma samples
Dataset
EGAD50000002166
-
Phenotype Risk Scores Identify Patients with Unrecognized Mendelian Disease Patterns
Study
phs001516
-
Cancer-associated fibroblasts promote drug resistance in ALK-driven lung adenocarcinoma cells by upregulating lipid biosynthesis
Study
EGAS50000000135
-
Enhanced Adjuvanticity of a Personal Neoantigen Vaccine Generates Potent Neoantigen-Specific Immunity
Study
phs003919
-
Whole genome sequencing with linked reads of pediatric glioblastoma samples
Study
EGAS00001003432
-
Probabilistic cell type assignment of single-cell transcriptomic data reveals spatiotemporal microenvironment dynamics in human cancers
Study
EGAS00001003452
-
Small variants in mtDNA Canary Islands - WES Illumina (ITER)
Study
EGAS00001005678
-
Small variants in mtDNA Canary Islands - WGS Illumina (ITER)
Study
EGAS00001005679
-
Small variants in mtDNA Canary Islands - WGS Oxford Nanopore Technologies (ITER)
Study
EGAS00001005677
-
Immunoprotective mechanisms and microbiota interplay in Salmonella Typhi infection
Study
phs001521
-
Metastatic Prostate Follow Up 2
Dataset
EGAD00001000989
-
CPC-GENE Prostate Cancer Heterogeneity Study
Dataset
EGAD00001002885
-
CRLF2 sequencing project Exomes
Dataset
EGAD00001000077
-
Functional characterisation of CpG islands in human tissues
Dataset
EGAD00001000212
-
WGS
Dataset
EGAD00001001120
-
Molecular Genetics of Histiocytic Sarcoma
Study
phs001748
-
Integrative genome profiling in AML
Dataset
EGAD00001001873
-
Melanoma multi site metastases
Dataset
EGAD00001005487
-
All counts
Dataset
EGAD50000001715
-
WES of melanoma tumors treated with combined immune checkpoint blockade
Study
EGAS00001003857
-
Single nucleus RNA Seq of LUAD patient derived lung samples
Dataset
EGAD00001008955
-
Clonal somatic copy number altered driver events inform drug sensitivity in high-grade serous ovarian cancer.
Dataset
EGAD00001008716
-
Comparison of 3 protocols for deriving pancreatic progenitors from hPSCs (RNA-seq)
Dataset
EGAD00001004823
-
Sequencing data for oesophageal and related samples - ICGC DCC release 26 (WGS)
Dataset
EGAD00001003580
-
Patient Microbiome and Surgical Site Infection in Spine Surgery
Study
phs003358
-
Anaplastic meingioma methylation
Dataset
EGAD00010001629
-
Error-corrected sequencing of 26 driver genes
Dataset
EGAD50000000079
-
WGS in insulinomas
Dataset
EGAD50000000464
-
HGSOC genome-wide SNP (project ITH)
Dataset
EGAD00010002482
-
Melanoma multi site metastases
Dataset
EGAD00001005483
-
Environmental Arsenic and Diabetes Mellitus (Chihuahua Cohort)
Study
phs002139
-
Gut metagenomic data of 2,338 Pinggu adults
Study
EGAS00001004820
-
Pancreatic adenocarcinoma QCMG 20110901
Dataset
EGAD00001000049
-
Bulk RNA-seq of ATCWGS42 PDX models
Dataset
EGAD50000002145
-
Error-corrected sequencing of 26 driver genes (additional cohort)
Dataset
EGAD50000000641
-
RNAseq dataset
Dataset
EGAD50000001243
-
Whole Exome Sequencing
Dataset
EGAD00001011117
-
A Phase II Neoadjuvant Study of Palbociclib in Combination with Letrozole and Trastuzumab as Neoadjuvant Treatment of Stage II-III ER+ HER2+ Breast Cancer (PALTAN)
Study
phs003147
-
Count Me In (CMI): The Angiosarcoma (ASC) Project (CMI-ASCproject)
Study
phs001931
-
Transposable Elements in FTLD-TDP and ALS-TDP
Study
phs001889
-
Count Me In (CMI): The Metastatic Breast Cancer (MBC) Project (CMI-MBCproject)
Study
phs001709
-
Durable clinical impacts and mechanisms of action and resistance in histone K27 methylation-targeting epigenetic therapy
Study
JGAS000553
-
Prediction and quantification of splice events from RNA-seq data
Study
EGAS00001001026
-
The University of Hong Kong Intestinal Metaplasia Organoids Study
Study
EGAS00001007899
-
Childhood Cancer Model Atlas
Study
EGAS00001006320
-
WES of der(1;7)(q10;p10) myeloid neoplasms
Study
EGAS50000000704
-
Long-read and short-read isoform sequencing in breast cancer
Study
EGAS00001004819
-
Sequencing data for oesophageal and related samples - OACs release 2 (RNA)
Dataset
EGAD00001003839
-
Exome reads and RNA-seq
Dataset
EGAD00001002722
-
RNAseq
Dataset
EGAD00001006008
-
Prostate cancer datasets WES
Dataset
EGAD00001004467
-
PGRN-Leducq: Identification of the KCNE1 D85N Polymorphism as a Possible Modulator of Drug-Induced Torsades de Pointes
Study
phs000617
-
IKZF5 RNAseq samples for platelets, neutrophils, monocytes and CD4+ T-cells.
Dataset
EGAD00001005107
-
alopecia areata
Dataset
EGAD00001006370
-
Metastatic Adrenocortical Carcinoma Displays Higher Mutation Rate and Tumor Heterogeneity than Primary Tumors
Study
phs001658
-
Melanoma_multi_site_metastases
Study
EGAS00001001348
-
Prostate cancer datasets WGS
Dataset
EGAD00001004466
-
Multi-site tumor sampling highlights molecular intra-tumor heterogeneity in malignant pleural mesothelioma
Dataset
EGAD00001007762
-
Exome-sequencing of human B cell lymphoma cell lines
Study
EGAS00001001463
-
Searching for variants associated with endometriosis
Study
EGAS00001001741
-
CTCF-dependent enhancer hijacking by the EVI1 oncogene in leukemia
Study
EGAS00001004808
-
The Genetic Landscape of Ocular Adnexa MALT Lymphoma Reveals Frequent Aberrations in NFAT and MEF2B Signaling Pathways
Study
EGAS00001006631
-
Transcriptomic profiling of patient-derived xenografts and organoids in prostate cancer
Dataset
EGAD00001006404
-
Whole_genome_sequencing_of_100_DDD_trios_with_suspected_noncoding_causal_mutations
Study
EGAS00001002452
-
Genetic Basis of Developmental Disabilities
Study
phs000337
-
Systems Analysis of the PfSPZ Vaccine in Kenyan Infants
Study
phs002196
-
Analysis of Somatic Mutations in Pediatric AML FAB-M7 Subtype by Whole Transcriptome Sequencing
Study
phs000413
-
Type 1 Diabetes Genetics Consortium (T1DGC): Copy Number Variant (CNV) Study
Study
phs000910
-
Tourette International Collaborative Genetics (TIC Genetics) Study - NJCTS and NIMH
Study
phs001423
-
Germline Genomic Analyses of Breast Cancer in Latinas
Study
phs003144
-
Somatic Mutation in Normal Bladder Study
Study
phs004105
-
Resolving the Full Spectrum of Human Genome Variation using Linked-Reads
Study
EGAS00001003121
-
Circulating Tumor DNA in Checkpoint Inhibitor treated Lung Cancer
Study
EGAS00001004847
-
Ultra-Fast Patient-Derived Xenografts Identify Functional and Spatial Tumour Heterogeneities that Drive Therapeutic Resistance
Study
EGAS00001002627
-
Tracking the evolution of Therapy-Related Myeloid Neoplasms using chemotherapy signatures
Study
EGAS00001006903
-
We evaluate the potential for routine WGS using ONT by sequencing the well-characterised reference sample NA12878 and the genome of an individual with ataxia-pancytopenia syndrome accompanied by severe immune dysregulation.
Study
EGAS00001003469
-
Characterization of DLBCL with a PMBL gene expression signature
Study
EGAS00001005057
-
Whole genome sequencing of tumor samples from advanced pre-treated NSCLC patients recruited in a phase I/II single-arm trial utilising CVA21, an oncolytic coxsackie virus, in combination with pembrolizumab.
Study
EGAS00001008258
-
POT1_splice_site_mutant_analysis
Study
EGAS00001000571
-
Single-Cell TCR/BCR Sequencing for Korean COVID-19 Vaccinated and Patient Samples
Study
phs003341
-
De Novo Characterization of Cell-Free DNA Fragmentation Hotspots in Plasma Whole-Genome Sequencing
Study
phs003062
-
NIH RECOVER: A Multi-Site Pathology Study of Post-Acute Sequelae of SARS-CoV-2 Infection
Study
phs003768
-
Long-read-transcriptome-sequencing of CLL and MDS patients uncovers common molecular effects of SF3B1 mutations
Study
EGAS50000000053
-
WES dataset of a TIL-ACT metastatic melanoma cohort
Dataset
EGAD50000001731
-
Spatial heterogeneity of follicular lymphoma
Dataset
EGAD00001003553
-
Andersen-Tawil Syndrome: Genotype-phenotype correlation and longitudinal study
Study
phs001289
-
The PUWMa (
Study
phs000358
-
HGG panel sequencing
Study
EGAS50000000221
-
Understanding Determinants of Racial Disparities in Lung Cancer Incidence
Study
phs003789
-
RNAseq of 76 samples from Uveal Melanoma tumors
Study
EGAS00001002932
-
Single-cell RNA sequence analysis of iPS cell-derived cardiomyocytes treated with S-RBD-sfGFP or GFP
Study
JGAS000620
-
High-depth whole genome sequencing of paired ductal carcinoma in-situ (DCIS) and germline control samples from 26 individuals.
Dataset
EGAD50000002237
-
RNA-Sequencing and Somatic Mutation Status of Adrenocortical Tumors: Novel Pathogenetic Insights
Study
EGAS00001004533
-
Breast Cancer Single-Cell RNA-Seq Dataset
Dataset
EGAD00001007495
-
WGS datasets of pediatric glioblastoma
Dataset
EGAD00001005212
-
DIPG WES and RNA-Seq
Dataset
EGAD00001006450