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Genetic makeup of agnospheres
Study
EGAS00001004868
-
Gene_Characterization_in_Carbohydrate_metabolic_alterations__neonatel_diabetes___congenital_hyperinsulinemic__in_early_childhood
Study
EGAS00001002074
-
Functional analysis of GATA2 synonymous mutations
Study
EGAS00001003817
-
Mutational analysis of an oligoprogressive sarcomatoid hepatocellular carcinoma treated with an immune checkpoint inhibitor.
Study
EGAS00001005064
-
RNA sequencing CYLD cutaneous syndrome
Study
EGAS00001003841
-
Same-day genomic and epigenomic diagnosis of brain tumors using realtime nanopore sequencing
Study
EGAS00001002213
-
Illumina Omni5 SNP chip genotyping of MacTel cases and unaffected controls for a genome-wide association study
Study
EGAS00001002249
-
Genetic_vulnerability_of_knockout_cancer_lines
Study
EGAS00001002253
-
Single_Cell_RNAseq_at_various_stages_of_HiPSCs_differentiating_toward_definitive_endoderm_and_endoderm_derived_lineages
Study
EGAS00001002278
-
Genetic landscape of inherited retinal dystrophies affected cases in Spain
Study
EGAS00001005104
-
Discovering genetic causes of optic atrophy syndromes through whole exome sequencing
Study
EGAS00001003850
-
Single cell phenotypic profiling of 27 DLBCL cases reveals marked inter- and intra-tumoral heterogeneity
Study
EGAS00001003860
-
Chronic myelomonocytic leukemia
Study
EGAS00001005107
-
Epigenomic profiling and transcriptomic profiling of LUAD patients tumor tissues and tumor adjacent tissues
Study
EGAS00001005132
-
Biological insights from the whole genome sequences of human embryonic stem cell lines
Study
EGAS00001002400
-
Comprehensive investigation of genome architecture of papillary thyroid cancer with whole-exon sequencing in the Chinese population.
Study
EGAS00001002402
-
Cell-free DNA TAPS for early cancer detection
Study
EGAS00001004962
-
Whole exome sequencing in patients with ALS and concomitant FTD lacking the C9orf72 repeat expansion
Study
EGAS00001002439
-
Comprehensive Molecular Analysis of Colon Cancer for the Identification and Validation of New Biomarkers
Study
EGAS00001002453
-
Genomic Profiling Reveals Spatial Intra-tumour Heterogeneity in Follicular Lymphoma
Study
EGAS00001002492
-
ATRX mutant neuroblastoma is sensitive to EZH2 inhibition via modulation of neuronal differentiation.
Study
EGAS00001002507
-
Distinct genomic profile and specific targeted drug responses in adult cerebellar glioblastoma
Study
EGAS00001002517
-
Linking the epigenetic landscape in chronic lymphocytic leukemia to deregulated chromatin networks
Study
EGAS00001002518
-
Single-cell landscapes of primary glioblastomas and matched organoids and cell lines reveal variable retention of inter- and intra-tumor heterogeneity
Study
EGAS00001005227
-
The aim of this study was to identify underlying hub genes and dysregulated pathways associated with the development of HCC using bioinformatics analysis.
Study
EGAS00001002526
-
Integrative genomic analysis identifies multiple subtypes and therapeutic targets in acute erythroid leukemia
Study
EGAS00001002537
-
The genomic landscape of childhood acute lymphoblastic leukaemia with intrachromosomal amplification of chromosome 21 (iAMP21-ALL)
Study
EGAS00001004998
-
Single-cell RNA sequencing reveals cell-type specific eQTLs in peripheral blood mononuclear cells
Study
EGAS00001002560
-
Genetic history of the Comorian populations.
Study
EGAS00001002565
-
H3Africa - An integrated approach to the identification of genetic determinants of susceptibility to trypanosomiasis
Study
EGAS00001002602
-
Genetic heterogeneity and dynamics of transcriptional subtypes in matched primary and recurrent head and neck squamous cell carcinomas
Study
EGAS00001005005
-
Host genetic determinants of HIV infection
Study
EGAS00001005245
-
The Southern African Human Genome Programme
Study
EGAS00001002639
-
Radiation-induced gliomas represent H3-/IDH-wild type pediatric gliomas with recurrent PDGFRA amplification and loss of CDKN2A/B
Study
EGAS00001005243
-
Transcriptomic and epigentic analysis of human peripheral blood NK cell subsets revealing role of Bcl11b in differentiation
Study
EGAS00001005025
-
Defining the metastasome in colorectal cancer: Implications for hypotheses on metastasis evolution and personalized therapy (HIPO-032)
Study
EGAS00001002717
-
Defective Homologous Recombination DNA Repair as Therapeutic Target in Advanced-Stage Chordoma (HIPO_021)
Study
EGAS00001002720
-
The_British_Autozygosity_Populations_BioResource
Study
EGAS00001002742
-
The molecular basis of T-PLL is an actionable perturbation of TCL1/ATM- and epigenetically instructed damage responses
Study
EGAS00001002744
-
Genomic landscape of inflammatory breast cancer by whole-genome sequencing
Study
EGAS00001004117
-
Multiple migrations to the Philippines during the last 50,000 years
Study
EGAS00001005083
-
Whole genome sequencing of 76 tumor and normal samples from 11 SI-NET patients
Study
EGAS00001005096
-
Phylogenetic analysis of treatment-naive metastases using whole exome and genome sequencing data
Study
EGAS00001002777
-
Indonesian RNA-seq data
Study
EGAS00001003671
-
Evolutionary predictability of genetic versus non genetic resistance to anticancer drugs in melanoma
Study
EGAS00001005314
-
MutWP4__CRUK_Grand_Challenge_Mutographs_of_Cancer__Gastric_Organoids
Study
EGAS00001003151
-
DNA hypermethylation and differential gene expression associated with Klinefelter syndrome
Study
EGAS00001002797
-
Whole-exome sequencing of Fanconi anemia-like inherited bone marrow failure syndrome
Study
EGAS00001003809
-
MutWP1__CRUK_Grand_Challenge_Mutographs_of_Cancer__Oesophageal_adenocarcinoma
Study
EGAS00001003702
-
Whole-Genome Sequencing of Salivary Gland Adenoid Cystic Carcinoma
Study
EGAS00001002812