-
Single Cell Genome Sequence for DLP+ library A96113A
Dataset
EGAD00001009453
-
Single Cell Genome Sequence for DLP+ library A96175A
Dataset
EGAD00001009461
-
A96120A
Dataset
EGAD00001007640
-
Single Cell Genome Sequence for DLP+ library A95652B
Dataset
EGAD00001009327
-
A95623B
Dataset
EGAD00001007608
-
A96155C
Dataset
EGAD00001007617
-
A110673A
Dataset
EGAD00001007602
-
Single Cell Genome Sequence for DLP+ library A96205B
Dataset
EGAD00001009471
-
A108732A
Dataset
EGAD00001007592
-
A110618A
Dataset
EGAD00001007599
-
Exome and Targeted sequencing of GZL
Dataset
EGAD00001006328
-
Single Cell Genome Sequence for DLP+ library A95717B
Dataset
EGAD00001009489
-
Mucosal 16S sequencing data
Dataset
EGAD00001008843
-
Reference exome data for a Northern Brazilian population
Dataset
EGAD00001006407
-
A96149B
Dataset
EGAD00001008235
-
Single Cell Genome Sequence for DLP+ library A96161A
Dataset
EGAD00001009457
-
10x Genomics Single Cell Gene Expression for SA1055
Dataset
EGAD00001009111
-
10x Genomics Single Cell Gene Expression for SA1053FX1XB01611
Dataset
EGAD00001009128
-
10x Genomics Single Cell Gene Expression for SA1096CX1XB02039
Dataset
EGAD00001009136
-
10x Genomics Single Cell Gene Expression for SA1035X5XB03021
Dataset
EGAD00001009153
-
A96118A
Dataset
EGAD00001007113
-
Whole exome sequencing of human and mouse sarcoma samples for personalized therapy
Dataset
EGAD00001004885
-
10x Genomics Single Cell Gene Expression for SA1051DX1XB01482
Dataset
EGAD00001009133
-
Single Cell Genome Sequence for DLP+ library A118816A
Dataset
EGAD00001009444
-
Single Cell Genome Sequence for DLP+ library A96200B
Dataset
EGAD00001009470
-
Single Cell Genome Sequence for DLP+ library A96194A
Dataset
EGAD00001009468
-
Single Cell Genome Sequence for DLP+ library A96194B
Dataset
EGAD00001009469
-
Single Cell Genome Sequence for DLP+ library A96222A
Dataset
EGAD00001009478
-
Single Cell Genome Sequence for DLP+ library A96206B
Dataset
EGAD00001009472
-
Single Cell Genome Sequence for DLP+ library A96207A
Dataset
EGAD00001009473
-
Single Cell Genome Sequence for DLP+ library A96141A
Dataset
EGAD00001009513
-
single-cell RNAseq FASTq files for three muscle-invasive bladder tumors
Dataset
EGAD00001008001
-
Dataset for transcriptome sequencing of chordoma cells
Dataset
EGAD00001015642
-
RNA-Seq data for manuscript titled: CBL0137 impairs homologous recombination repair and sensitizes high-grade serous ovarian carcinoma to PARP inhibitors Sequencing
Dataset
EGAD00001009799
-
KiCS WGS data for academic use only
Dataset
EGAD00001009698
-
A118845B
Dataset
EGAD00001007098
-
A98295B
Dataset
EGAD00001007132
-
A98234A
Dataset
EGAD00001007626
-
A118862A
Dataset
EGAD00001007605
-
Single Cell Genome Sequence for DLP+ library A96190B
Dataset
EGAD00001009466
-
Single Cell Genome Sequence for DLP+ library A96207B
Dataset
EGAD00001009474
-
Thymic epithelial transplantation for complete DiGeorge syndrome Spatial (2026-01-19)
Dataset
EGAD00001015798
-
Single Cell Genome Sequence for DLP+ library A98240A
Dataset
EGAD00001009480
-
Transcriptomic profiles of neuroblastoma PDXs and primary tumors
Dataset
EGAD00001003393
-
Whole Genome Sequencing (WGS) for St. Jude High Grade Glioma (HGG) study
Dataset
EGAD00001000806
-
V4 panel bait design test (2018-03-07)
Dataset
EGAD00001004001
-
Whole exome sequencing data for patients with Bosma arhinia microphthalmia syndrome (BAMS)
Dataset
EGAD00001003130
-
Exome sequencing of patients with acute promyelocytic leukemia
Dataset
EGAD00001004043
-
Whole Exome Sequencing (WES) for St. Jude High Grade Glioma (HGG) study
Dataset
EGAD00001000807
-
Exome and Transcriptome for pan-cancer gene-drug analysis
Dataset
EGAD00001003441
-
ICGC-LIRI-JP Release 16
Dataset
EGAD00001000842
-
BLUEPRINT release January 2015, DNase-Hypersensitivity for monocyte
Dataset
EGAD00001001185
-
Cram files for study entitled Compound heterozygous variants in LAMC3 in association with posterior periventricular nodular heterotopia
Dataset
EGAD00001006578
-
RNA-seq, ChIP-seq, ATAC-seq files for PCGP SJERG
Dataset
EGAD00001002681
-
Exome sequencing of Non-syndromic Congenital Heart Defects (2019-04-24)
Dataset
EGAD00001004972
-
Exome sequencing of Non-syndromic Congenital Heart Defects (2019-04-24)
Dataset
EGAD00001004975
-
A95646A
Dataset
EGAD00001007106
-
Profiling Chromatin Accessibility in Humans Using Adenine Methylation and Long-Read Sequencing
Dataset
EGAD00001015374
-
DNA WGS Long Read Sequence (PromethION) for manuscript titled: "Performance of Somatic Structural Variant Calling in Lung Cancer using Oxford Nanopore Sequencing Technology"
Dataset
EGAD00001015400
-
Transcriptomic data for Human proximal tubular epithelial cell interleukin-1 receptor signalling triggers cell cycle arrest during hypoxic kidney injury
Dataset
EGAD00001015460
-
Longitudinal Study of Fluoride and Other Factors Related to Dental Fluorosis, Dental Caries, and Bone Health
Study
phs002203
-
Development of molecular targeted therapy for small cell lung cancer by comprehensive genome analysis
Study
JGAS000037
-
Exome array analysis of adverse reactions to fluoropyrimidine-based therapy for gastrointestinal cancer
Study
EGAS00001002763
-
Molecular Biomarkers in Glioma (Mechanisms and Therapeutic Implications of Hypermutation in Gliomas)
Study
phs001967
-
Primary Prostate Tumor Tissue DNA Methylation Profiles
Study
phs001921
-
Comprehensive Epigenetic Landscape of Rheumatoid Arthritis Fibroblast-Like Synoviocytes
Study
phs001615
-
Multicenter Study of Hydroxyurea (MSH)
Study
phs002348
-
CSER: Exome Sequencing in Diverse Populations in Colorado and Oregon/CHARM Cancer Health Assessments Reaching Many
Study
phs002111
-
Comprehensive molecular profiling identifies novel genetic drivers and subtypes underlying medulloblastoma
Study
EGAS00001001953
-
scRNA-seq of HSPC treated with gemcitabine and carbplatin
Study
EGAS00001004381
-
The International Consortium for Prostate Cancer Genetics Genome Wide Association Study of Familial Prostate Cancer
Study
phs000733
-
Genomic and Transcriptomic sequencing of neuroblastoma cell lines
Dataset
EGAD50000000729
-
Comparison of fresh and slow-frozen cancer samples for different applications
Study
EGAS00001005891
-
Oxford Nanopore RNA sequencing for HLA typing
Study
EGAS00001004918
-
MicroRNA profiling by next-generation sequencing for colorectal cancer screening
Study
EGAS00001005030
-
RNA sequencing data for Molecular Characterization of ETMRs
Dataset
EGAD00001006209
-
scRNA-seq using 10X Genomics platform
Dataset
EGAD00001006974
-
cfMeDIP data for 72 VPC samples for validation
Dataset
EGAD00001008737
-
Sequencing data for oesophageal and related samples - Ogden et al (WGS, RNA)
Dataset
EGAD00001007496
-
Molecular and phenotypic data for patients enrolled in the IMmotion150 trial
Dataset
EGAD00001004183
-
PKD1 capture-by-hybridization resequencing for genetic diagnostics of polycystic kidney disease
Dataset
EGAD00001001091
-
Transcriptome and Exome from longitudinal samples of human glioblastoma
Dataset
EGAD00001001424
-
BLUEPRINT September 2016, ChIPmentation for effector memory CD8-positive, alpha-beta T cell, terminally differentiated from venous blood, on Genome GRCh38
Dataset
EGAD00001002943
-
BLUEPRINT September 2016, ChIP-Seq for class switched memory B cell from venous blood, on Genome GRCh38
Dataset
EGAD00001002951
-
Prediction of Trastuzumab Benefit in Adjuvant Breast Cancer: Gene Expression Profiling in NSABP B31
Study
phs000826
-
Next-Generation Sequencing of RNA and DNA Isolated from Paired Fresh-Frozen and Formalin-Fixed Paraffin-Embedded Samples of Human Cancer and Normal Tissue
Study
EGAS00001000737
-
Characterization of genetic intratumor heterogeneity in colorectal cancer and matching patient-derived spheroid cultures.
Study
EGAS00001002684
-
Endometrial Cancer Association Consortium - OncoArray Genotypes
Study
phs001885
-
NCT03343197: Clinical Biomarker Data
Study
phs003148
-
Segmental Overgrowth/Vascular Anomalies/Dermatologic Disorders
Study
phs002006
-
Ontario Familial Colon Cancer Registry Single Nucleotide Polymorphisms and CpG Methylation (OFCCR SNP-CpG)
Study
phs000779
-
CCG Multicentric Italian Lung Detection (MILD)
Study
phs002253
-
Transcriptome HCCO Hypoxia and Doxorubicin resistance
Study
EGAS50000000042
-
A first step towards clinical routine long-read sequencing in Sweden, a national pilot study on chromosomal rearrangements
Study
EGAS50000000468
-
A Large-Scale, Consortium-Based Genomewide Association Study of Asthma
Study
EGAS00000000077
-
Atezolizumab and Bevacizumab in Treating Patients With Rare Solid Tumors
Study
phs003845
-
Childhood Cancer Data Initiative (CCDI): Pediatric In Vivo Testing Program – Sarcomas and other Solid Tumors
Study
phs003161
-
Genome and transcriptome sequencing of cancer of unknown primary tumours
Study
EGAS50000000452
-
Emirati Diploid Single Samples Assemblies
Study
EGAS50000001233
-
Emirati Phased Diploid Trio-Assemblies
Study
EGAS50000001234