-
DNA methylation and the adverse metabolic outcomes of adiposity
Study
EGAS00001001922
-
Immunodeficiency syndrome caused by LCP1 mutations
Study
EGAS00001008293
-
The genomic landscape of pediatric acute lymphoblastic leukemia
Study
EGAS00001005250
-
Methylation differences in trisomy 21 using monozygotic twins
Study
EGAS00001001051
-
A targeted gene panel that covers coding, noncoding, and short tandem repeat regions improves the diagnosis of patients with neurodegenerative diseases
Study
EGAS00001003737
-
Organoid cultures of early-onset colorectal cancers reveal distinct and rare genetic profiles
Study
EGAS00001004063
-
Single cell RNA-seq mapping of nasal and tracheobronchial airways in human healthy volunteers
Study
EGAS00001004082
-
Targeted and shallow whole genome sequencing identifies therapeutic opportunities in p53abn endometrial cancers
Study
EGAS00001007661
-
Pediatric Papillary Thyroid Carcinoma Whole Exome Sequencing
Study
EGAS00001005187
-
WES analysis of a mixed cohort of pituitary tumors
Study
EGAS00001001714
-
High-Resolution Spatial Transcriptomics Uncover Epidermal-Dermal Divergences in Merkel Cell Carcinoma: Spatial Context Reshapes the Gene Expression Landscape
Study
EGAS00001008157
-
C3 SNPs and outcome after lung transplantation
Study
EGAS00001003843
-
whole genome sequence data of multifocal hepatocellular carcinoma
Study
EGAS00001002338
-
Analysis of recent shared ancestry in a familial cohort identifies coding and noncoding autism spectrum disorder variants
Study
EGAS00001006058
-
Somatic mutations predict an aggressive phenotype in meningioma but do not drive grade progression
Study
EGAS00001006585
-
Microsatellite data show recent demographic expansions in sedentary but not in nomadic human populations in Africa and Eurasia.
Study
EGAS00001000652
-
Clinical relevance of somatic copy-number alterations in plasma circulating tumor DNA from advanced EGFR-mutated NSCLC patients treated with osimertinib
Study
EGAS00001004539
-
High-throughput Detection of Clinically Relevant Mutations in Archived Tumor Samples By Multiplexed PCR and Next Generation Sequencing
Study
EGAS00001000674
-
Combination of ribociclib and gemcitabine for the treatment of medulloblastoma
Study
EGAS00001006001
-
Study of the rare and low frequency variants in the Saguenay-Lac-Saint-Jean population
Study
EGAS00001003103
-
Oncogenic fate conversion by PRDM16s causes acute myeloid leukemia
Study
EGAS00001003235
-
Implementation of pediatric precision oncology into clinical practice: The individualized Therapies for Children with cancer program “iTHER”
Study
EGAS00001007099
-
Exome sequencing of uterine leiomyosarcomas
Study
EGAS00001001612
-
RB Loss in Resistant EGFR Mutant Lung Adenocarcinomas that Transform to Small Cell Lung Cancer
Study
EGAS00001001102
-
Spatiotemporal evolution and inter-patient heterogeneity in primary and recurrent/metastatic head and neck squamous cell carcinoma
Study
EGAS00001007464
-
Neoadjuvant immunotherapy leads to pathological responses in MMR proficient and MMR deficient early stage colon cancers
Study
EGAS00001004160
-
pancreatic ductal adenocarcinoma exomes in study: Pro-immunogenic Impact of MEK inhibition combined with an anti-CD40 immunostimulatory antibody
Study
EGAS00001004196
-
Genome-Wide Association Study of aspirin-induced PUD in a UK cohort
Study
EGAS00001002052
-
Search for new loci and low-frequency variants influencing glioma risk by exome-array analysis
Study
EGAS00001001258
-
Circumventing intratumoral heterogeneity to identify potential therapeutic targets in hepatocellular carcinoma. Details please contact lifuqiang@genomics and zhaoxin@genomics.cn.
Study
EGAS00001002207
-
Aging and genome-wide patterns of DNA methylation in an African rainforest hunter-gathering population
Study
EGAS00001002226
-
Poly(A) RNA sequencing of hepatocellular carcinoma tumors and their matched noncancerous liver tissues
Study
EGAS00001002337
-
Genomic consequences of aberrant DNA repair mechanisms stratify ovarian cancer histotypes
Study
EGAS00001002390
-
Recurrent epimutations activate gene body promoters in primary glioblastoma
Study
EGAS00001000685
-
Benchmarking for alignment and variant calling
Study
EGAS00001007819
-
A Functional Network of Gastric-Cancer-Associated Splicing Events Controlled by Dysregulated Splicing Factors
Study
EGAS00001002256
-
Exome Sequencing Of 75 Individuals From Multiply Affected Coeliac Families
Study
EGAS00001001093
-
Differential Presence of Exons in Cell-Free DNA Reveals Different Patterns in Colorectal Cancer Between Metastatic and Non-Metastatic Patients
Study
EGAS00001002687
-
UK10K NEURO FSZNK
Study
EGAS00001000119
-
UK10K NEURO ASD SKUSE
Study
EGAS00001000114
-
Sequencing-based counting and size profiling of plasma Epstein-Barr virus DNA enhance population screening of nasopharyngeal carcinoma.
Study
EGAS00001002707
-
Neoantigen responses to Immunotherapy in Prostate Cancer
Study
EGAS00001004050
-
UK10K_NEURO_MUIR
Study
EGAS00001000122
-
Characterization of a human iPSC-derived islet differentiation model
Study
EGAS00001002721
-
TRACERx 100: whole exome data of the first 100 TRACERx tumours
Study
EGAS00001002247
-
Breast cancer DNA repair
Study
EGAS00001002792
-
A_systems_biology_approach_to_understand_immunity_and_pathogenesis_of_malaria_in_children_exposed_to_endemic_Plasmodium_falciparum_transmission
Study
EGAS00001002978
-
Biallelic tumor suppressor loss and DNA repair defects in de novo small cell prostate cancer
Study
EGAS00001003007
-
Open_Targets_020_Epigenomes_of_Cell_Lines
Study
EGAS00001003136
-
A Single Complex Agpat2 Allele In A Patient With Partial Lipodystrophy
Study
EGAS00001003177
-
Structure and evolution of double minutes in diagnosis and relapse brain tumors
Study
EGAS00001003212
-
Longitudinal_profiling_of_the_immune_response_to_Plasmodium_vivax_in_naive_hosts_by_RNA_sequencing
Study
EGAS00001003847
-
MYCN Amplification and ATRX Mutations are Incompatible in Neuroblastoma
Study
EGAS00001003257
-
These are from Korean HCC samples with exome sequencing
Study
EGAS00001000604
-
Chromatin immunoprecipitation linked to next-generation whole genome sequencing (ChIP-Seq) for H3K36me3 in paediatric high grade glioma cell lines KKNS4 and SF188 with and without a G34V mutation in H3F3A
Study
EGAS00001001437
-
Spatial and temporal evolution of distal 10q deletion, a prognostically unfavorable event in diffuse low-grade gliomas
Study
EGAS00001000643
-
Study on the consequences of prenatal famine exposure on DNA methylation.
Study
EGAS00001000668
-
Dilgom_Exome
Study
EGAS00001000086
-
Quantification of chromosomal copy number aberrations by shallow whole-genome sequencing
Study
EGAS00001000642
-
Prediction and quantification of splice events from RNA-seq data
Study
EGAS00001001026
-
Comparison of the diagnostic yield of aCGH and NGS across different neurodevelopmental disorders
Study
EGAS00001004949
-
Expanding the neurodevelopmental phenotypes of individuals with de novo KMT2A variants
Study
EGAS00001003521
-
Prediction of pigmentation phenotypes by SNP typing in a Northern German population
Study
EGAS00001001174
-
Single-cell DNA amplicon sequencing reveals clonal heterogeneity and evolution in T-cell acute lymphoblastic leukemia
Study
EGAS00001004440
-
Associations between APOE status and cognitive ability across the lifecourse
Study
EGAS00001001235
-
Transcriptome_human_nasal_epithelium
Study
EGAS00001001294
-
UK10K_RARE_THYROID
Study
EGAS00001000131
-
A unidirectional histone code in bidirectional promoters across cell types
Study
EGAS00001001656
-
Healthspan and lifespan extension by fecal microbiota transplantation in progeroid mice
Study
EGAS00001003656
-
Detection of ctDNA in Plasma of Patients with Clinically Localised Prostate Cancer is Associated with Rapid Disease Progression
Study
EGAS00001004636
-
Molecular classification improves risk assessment in adult B-lineage ALL: Patients on the international UKALLXII-ECOG2993 trial.
Study
EGAS00001004638
-
Sporadic and endemic Burkitt lymphoma have frequent FOXO1 mutations but distinct hotspots in the AKT recognition motif
Study
EGAS00001003719
-
Evolution of a FLT3-TKD mutated subclone at meningeal relapse in acute promyelocytic leukemia (H021)
Study
EGAS00001001848
-
Next-Generation Sequencing of AV Nodal Reentry Tachycardia patients
Study
EGAS00001002745
-
Dynamics of genome architecture and chromatin function during human B cell differentiation and neoplastic transformation
Study
EGAS00001004763
-
Transcriptional profiling of ovarian tumours and cell lines
Study
EGAS00001004814
-
Colorectal cancer organoids expressing BRAF (fusion) genes
Study
EGAS00001003558
-
MYO5B mutations in Pheochromocytoma/Paraganglioma promote cancer progression
Study
EGAS00001003991
-
Phylogenetic analysis of treatment-naive metastases using whole exome and genome sequencing data
Study
EGAS00001002777
-
A novel breast cancer cell line derived from a metastatic bone lesion of a breast cancer patient
Study
EGAS00001002840
-
Colorectal adenomas, carcinomas and adjacent normal NKI-AvL TGO series NGS-ProToCol
Study
EGAS00001002854
-
Integrated clinical, whole genome, and transcriptome analysis of multisampled lethal metastatic prostate cancer
Study
EGAS00001001659
-
Clonal fitness inferred from timeseries modeling of single cell cancer genomes
Study
EGAS00001004448
-
Versatile workflow for cell-type resolved transcriptional and epigenetic profiles from cryopreserved human lung
Study
EGAS00001004477
-
Identification of Therapeutic Targets in Rhabdomyosarcoma Through Integrated Genomic, Epigenomic, and Proteomic Analyses
Study
EGAS00001002967
-
Detection and characterization of lung cancer using cell-free DNA fragmentomes
Study
EGAS00001005340
-
Human genomic and phenotypic synthetic data for the study of rare diseases
Study
EGAS00001005702
-
Open_Targets_020_Epigenomes_of_Cell_Lines
Study
EGAS00001003137
-
Open_Targets_020_Epigenomes_of_Cell_Lines
Study
EGAS00001003139
-
Healthy_ageing_thymus
Study
EGAS00001004311
-
Novel optineurin frameshift insertion causing familial frontotemporal dementia and parkinsonism without amyotrophic lateral sclerosis
Study
EGAS00001005220
-
Exome-wide mutation analysis of cell-free DNA to simultaneously monitor the full spectrum of cancer treatment outcomes
Study
EGAS00001005906
-
Transcriptome Sequencing PPGL
Study
EGAS00001006044
-
A higher ctDNA fraction decreases survival in regorafenib-treated metastatic colorectal cancer patients
Study
EGAS00001004491
-
Butyrate producers as potential next-generation probiotics: safety assessment of the administration of Butyricicoccus pullicaecorum to healthy volunteers
Study
EGAS00001003276
-
Transcriptomic intra-tumor heterogeneity of colorectal cancer varies depending on tumor location within the colorectum
Study
EGAS00001004668
-
Exome sequencing
Study
EGAS00001005761
-
Mutation-specific non-canonical pathway of PTEN as a distinct therapeutic target for glioblastoma
Study
EGAS00001004753
-
RaScALL: Rapid screening of RNA-seq in acute lymphoblastic leukaemia
Study
EGAS00001006460
-
Integrative genomic analysis identifies key pathogenic mechanisms in primary mediastinal large B-cell lymphoma
Study
EGAS00001003746