-
Genetic Heterogeneity of the familial gastric neuroendocrine tumors (2018-06-06)
Dataset
EGAD00001004153
-
WES analysis in identifying additive genetic factors that may contribute to the occurrence of moyamoya in neurofibromatosis type 1
Dataset
EGAD00001004157
-
Chromosome Segregation Errors Promote a Diverse Spectrum of Simple and Complex Genomic Rearrangements
Dataset
EGAD00001004163
-
RNA-seq analysis of transcriptome variation with human ESC subclones
Dataset
EGAD00001004266
-
IBD Whole Genome Sequencing Phase 1 (2018-08-03)
Dataset
EGAD00001004272
-
Comprehensive genetic analysis of Epstein-Barr virus-associated hematological malignancy
Dataset
EGAD00001004286
-
Genetic screening of GPI-anchor protein synthesis (2018-08-13)
Dataset
EGAD00001004294
-
Germline biallelic mutation affecting the transcription factor Helios causes pleiotropic defects of immunity
Study
EGAS00001005675
-
DERMATLAS__Porocarcinoma_WES
Study
EGAS00001005720
-
Genomic characterization of retinoblastoma (targeted sequencing)
Study
EGAS00001005550
-
Whole genome sequencing (bam files) of 5 samples of myxofibrosarcoma and 5 matched pairs
Study
EGAS00001005444
-
DERMATLAS__Poroma_WES
Study
EGAS00001007705
-
The PEMDAC phase 2 study of pembrolizumab and entinostat in patients with metastatic uveal melanoma
Study
EGAS00001005478
-
Duplexseq_of_the_interstrand_crosslinks_WGS
Study
EGAS00001006545
-
The_Little_Princess_Knowledge_Bank_RNAseq
Study
EGAS00001005244
-
Multi-site tumor sampling highlights molecular intra-tumor heterogeneity in malignant pleural mesothelioma
Study
EGAS00001005328
-
SG Peranakan Project: Genetic admixture in the culturally unique Peranakan Chinese population in Southeast Asia
Study
EGAS00001005379
-
Analysis of RAD51C promoter methylation using targeted bisulfite sequencing (amplicon sequencing) in ovarian cancer pre-clinical models and patient samples.
Study
EGAS00001005395
-
Germline RUNX1 Variation and Predisposition to Childhood Acute Lymphoblastic
Study
EGAS00001005403
-
MutWP4__CRUK_Grand_Challenge_Mutographs_of_Cancer__organoid_control_WGS
Study
EGAS00001005449
-
Multi-omics integration reveals only minor long-term molecular and functional sequelae in immune cells of individuals recovered from COVID-19
Study
EGAS00001005529
-
WGS_of_healhy_mesothelial_cells_and_primary_mesothelima_cell_lines
Study
EGAS00001005559
-
Mitochondrial DNA sequencing of iPSC, parental cells, and iPSC derived cardiomyocytes
Study
EGAS00001005560
-
Multiregional sequencing of IDH-WT glioblastoma reveals high genetic heterogeneity and a dynamic evolutionary history
Study
EGAS00001005128
-
Small variants in mtDNA Canary Islands - WGS Illumina (ITER)
Study
EGAS00001005679
-
DERMATLAS__Hidradenoma_papilliferum_RNAseq
Study
EGAS00001005715
-
Combination therapies to inhibit LCK tyrosine kinase and mTOR signaling in T-cell Acute Lymphoblastic Leukemia
Study
EGAS00001005945
-
H3K27me3-mediated epigenetic repression regulates neuroblastoma development and contributes to biological heterogeneity
Study
EGAS00001008225
-
Papuan Y chromosome Diversity Panel
Study
EGAS00001006025
-
CIRdb: Array genotype data
Study
EGAS00001006050
-
Analysis of recent shared ancestry in a familial cohort identifies coding and noncoding autism spectrum disorder variants
Study
EGAS00001006058
-
Chromatin profiles classify castration-resistant prostate cancers suggesting therapeutic targets
Study
EGAS00001006059
-
High-throughput telomere length measurement at nucleotide resolution using the PacBio high fidelity sequencing platform
Study
EGAS00001006103
-
Hematopoietic differentiation at single-cell resolution in NPM1-mutated AML
Study
EGAS00001006565
-
SARS-CoV-2 host genetics and COVID-19 outcomes in admixed Brazilians with extreme phenotypes
Study
EGAS00001006376
-
Molecular profiling of EBV associated diffuse large B-cell lymphoma
Study
EGAS00001006400
-
Cystic fibrosis multi-omics study
Study
EGAS00001006421
-
Multimodal Epigenetic Sequencing Analysis (MESA) of Cell-free DNA for Non-invasive Cancer Detection
Study
EGAS00001006462
-
Long-read sequencing of diagnosis and post-therapy medulloblastoma reveals complex rearrangement patterns and epigenetic signatures
Study
EGAS00001006576
-
GENOMIC MUTATION LANDSCAPE OF SKIN CANCERS FROM DNA REPAIR-DEFICIENT XERODERMA PIGMENTOSUM PATIENTS
Study
EGAS00001006732
-
MutWP1__CRUK_Grand_Challenge__matched_blood_Nanoseq
Study
EGAS00001006774
-
DNA methylation atlas of normal human cell types
Study
EGAS00001006791
-
Genome-wide DNA Methylation Analysis Reveals a Unique Methylation Pattern for Pleural Mesothelioma Compared to Healthy Pleura and Other Lung Diseases
Study
EGAS00001007783
-
A GWAS study with the AlpeDPD study cohort
Study
EGAS00001007855
-
Comprehensive epigenomic profiling reveals the extent of disease-specific chromatin states and informs drug target discovery in ankylosing spondylitis
Study
EGAS00001006945
-
Whole-genome sequencing across 449 samples spanning 47 ethnolinguistic groups provides insights into genetic diversity in Nigeria
Study
EGAS00001007036
-
Timing chromosomal amplification events using patterns of somatic mutations in high hyperdiploid acute lymphoblastic leukemia
Study
EGAS00001007052
-
BMP4 and temozolomide synergize in the majority of patient derived glioblastoma cultures
Study
EGAS00001007095
-
Effects of 2DG, Galactose, or Oligomycin on the epigenome remodeling induce by T cells activation.
Study
EGAS00001007115
-
Pediatric Papillary Thyroid Carcinoma Whole Exome Sequencing
Study
EGAS00001005187
-
H3Africa - An integrated approach to the identification of genetic determinants of susceptibility to trypanosomiasis
Study
EGAS00001007173
-
Nala GSI GSAv3 PGx Study
Study
EGAS00001007710
-
DERMATLAS__SG_basal_cell_adenoma_and_adenocarcinoma_WES
Study
EGAS00001007745
-
MutWP1__CRUK_Grand_Challenge__normal_kidney_Nanoseq
Study
EGAS00001005451
-
Genomic evolution and transcriptional changes in the evolution of prostate cancer into neuroendocrine and ductal carcinoma types (RNAseq)
Study
EGAS00001007428
-
mRNA capture sequencing and RT-qPCR for the detection of pathognomonic, novel and secondary fusion transcripts in formalin-fixed paraffin-embedded tissue: a sarcoma showcase
Study
EGAS00001005202
-
AfricanNeo aDNA Study
Study
EGAS00001007519
-
Genomic profiling of IBC
Study
EGAS00001007520
-
Epigenetic age deceleration reflects fitness improvements following a six-month endurance exercise intervention
Study
EGAS00001008221
-
DERMATLAS__Leiomyosarcoma_RNAseq
Study
EGAS00001007631
-
Comprehensive Deep Sequencing Atlas in HCC tumors
Study
EGAS00001007694
-
Double mutant DNMT3A AML: a unique subtype
Study
EGAS00001007966
-
Genomic Landscape and Clonal Architecture in Pediatric Myeloid Neoplasms with Chromosome 7 Deletions
Study
EGAS00001008055
-
Whole exome sequencing (bam files) of 55 samples of myxofibrosarcoma and 44 matched pairs
Study
EGAS00001005442
-
Pancreatic islets PISA RNA-seq samples
Study
EGAS00001005535
-
Understanding_the_development_of_resident_memory_T_cells__Trm__in_the_human_small_intestine_using_integrative_multiomic_approaches__Adult_RNA
Study
EGAS00001008257
-
DERMATLAS__Hidradenoma_papilliferum_WES
Study
EGAS00001005714
-
RNAseq_of_healthy_mesothelial_cells_and_primary_mesothelioma_cell_lines
Study
EGAS00001005728
-
Genetic variability in exon 1 of the glucocorticoid receptor gene NR3C1 is associated with postoperative complications
Study
EGAS00001005737
-
DERMATLAS__Poroma_RNAseq
Study
EGAS00001005759
-
Human induced pluripotent stem cells display a similar mutation burden as embryonic pluripotent cells in vivo
Study
EGAS00001005939
-
Molecular subtypes of pancreatic neuroendocrine tumors mutated in MEN1/DAXX/ ATRX explain biological variability
Study
EGAS00001008272
-
Immunodeficiency syndrome caused by LCP1 mutations
Study
EGAS00001008293
-
H3Africa - Deciphering Developmental Disorders in Africa
Study
EGAS00001008319
-
Ultrasensitive detection of minor allele fractions in maternal samples based on microhaplotype analysis
Study
EGAS00001007057
-
Long-term organoid culture of a small intestinal neuroendocrine tumor rna-seq
Study
EGAS00001007108
-
Bacterial SNPs in the human gut microbiome associate with host BMI
Study
EGAS00001007204
-
Spatiotemporal evolution and inter-patient heterogeneity in primary and recurrent/metastatic head and neck squamous cell carcinoma
Study
EGAS00001007464
-
Pediatric HGG WES and RNA-Seq
Study
EGAS00001005687
-
Taste Receptor Gene Variants: Body Mass Index (BMI) and Longevity
Study
EGAS00001008403
-
Single cell transcriptomic landscape of pediatric B-cell acute lymphoblastic leukemia: dissection of transcriptional heterogeneity and B-cell developmental state
Study
EGAS00001007512
-
Low-coverage whole genome sequencing for a highly selective cohort of severe COVID-19 patients
Study
EGAS00001007573
-
DERMATLAS__Leiomyosarcoma_WES
Study
EGAS00001007628
-
DERMATLAS__SG_basal_cell_adenoma_and_adenocarcinoma_RNAseq
Study
EGAS00001007746
-
Preclinical Pediatric Molecular Analysis for Therapy Choice (MATCH)
Study
EGAS00001008011
-
Ewing and Ewing-like-sarcoma tumoroid biobank reveals distinct drug sensitivities: translocation makes the difference
Study
EGAS00001007941
-
Whole exome and RNA sequencing of organoid samples derived from TRACERx patients
Study
EGAS00001008092
-
Raw bulk TCRseq data fromTIL and non-TIL expanded TRACERx samples in the manuscript Bulk TCRseq from TRACERx samples from 'Subclonal immune evasion in non-small cell lung cancer'
Study
EGAS00001008118
-
PacBio Rare Disease Study
Study
EGAS00001008170
-
The Human Phenotype Project (HPP) is a large-scale deep-phenotype prospective longitudinal and ethnically diverse cohort
Study
EGAS00001008040
-
Genetic characterization patients affected by Cancer of Unknown Primary
Study
EGAS00001006621
-
Discordant_Monozygotic_Twins_ALS (Epigenetics)
Study
EGAS00001008053
-
Genetics of male infertility in India
Study
EGAS00001008171
-
GCAT | Genomes for life: cohort study of the genomes of Catalonia
Study
EGAS00001003018
-
Comparison of the diagnostic yield of aCGH and NGS across different neurodevelopmental disorders
Study
EGAS00001004949
-
MutWP4__CRUK_Grand_Challenge_Mutographs_of_Cancer__Mutagen_treated_organoids
Study
EGAS00001004873
-
International Genetics of Parkinson Disease Progression (IGPP) Consortium GWAS Summary Results
Study
EGAS00001005110
-
Targeted sequencing of follicular lymphoma tumour samples from the UK's Haematological Malignancy Research Network
Study
EGAS00001005238
-
Bulk-tissue RNA-sequencing of anterior cingulate cortex samples derived from Lewy body disease patients
Study
EGAS00001005305
-
SmMIP-tools:a computational toolset for processing and analysis of single-molecule molecular inversion probes derived data
Study
EGAS00001005359