-
Search for new loci and low-frequency variants influencing glioma risk by exome-array analysis
Study
EGAS00001001258
-
Amplicon_based_sequencing_of_drug_resistant_organoids
Study
EGAS00001001639
-
Exploring_the_landscape_of_somatic_mutations_in_normal_tissue___POL___WGS
Study
EGAS00001003682
-
Kalirin-RAC controls nucleokinetic migration in ADRN-type neuroblastoma
Study
EGAS00001005023
-
Colorectal_Adenoma_Gene_Screen
Study
EGAS00001001261
-
Primary prostate Hi-C
Study
EGAS00001005014
-
Exome_Sequencing_of_Human_myeloid_malignancies
Study
EGAS00001001263
-
Korean Young Age Diffuse Gastric Cancers
Study
EGAS00001001711
-
Genomic characterization of esophageal squamous cell carcinoma reveals critical genes underlying tumorigenesis and poor prognosis
Study
EGAS00001001723
-
Recurrent adeno-associated virus 2-related insertional mutagenesis in human hepatocellular carcinomas
Study
EGAS00001001284
-
hereditary BrEAst Case CONtrol study
Study
EGAS00001005043
-
V2_panel_bait_design_test
Study
EGAS00001001780
-
Epigenome and transcriptome profiling of chronic lymphocytic leukemia patients
Study
EGAS00001001821
-
Genetic analysis of HLA and immune escape genes in Diffuse Large B-cell Lymphoma
Study
EGAS00001005054
-
Single-cell RNA-seq data from metastatic ovarian cancer for quality control study
Study
EGAS00001005066
-
Tumor-derived cell lines as pharmacogenomic models to predict therapeutic vulnerabilities in hepatocellular carcinoma
Study
EGAS00001003536
-
To_profile_the_landscape_of_sebaceous_tumours_WES
Study
EGAS00001003553
-
Amplicon_based_sequencing_of_drug_resistant_lung_cancer_cell_lines
Study
EGAS00001001675
-
Cancer-Associated Mutations in Endometriosis without Cancer
Study
EGAS00001003576
-
Stromal cell diversity associated with immune evasion in human triple‐negative breast cancer
Study
EGAS00001005061
-
Multi-omics analysis of primary glioblastoma cell-lines shows recapitulation of pivotal molecular features of parental tumors
Study
EGAS00001001871
-
Barcoding reveals complex clonal dynamics of de novo transformed human mammary cells
Study
EGAS00001001310
-
ENU_LS_411N_TripleTherapy
Study
EGAS00001001777
-
ENU_HT_29_BRAF_Triple_Therapy_Clones
Study
EGAS00001001778
-
The clonal and mutational evolution spectrum of primary triple negative breast cancers
Study
EGAS00001000132
-
Somatic_Genetics_of_lesions_from_a_POT1_patient
Study
EGAS00001001343
-
Enrichment of homologous recombination repair alteration in prostate cancer brain metastases
Study
EGAS00001005091
-
A somatic reference standard for cancer genome sequencing with COLO829
Study
EGAS00001001385
-
Transcriptional_Consequences_of_Copy_Number_Changes_MY_HDBR_200531
Study
EGAS00001005100
-
Breast Cancer - Subtype defined by an amplification of the HER2 gene
Study
EGAS00001001431
-
Whole-exome sequencing of human pancreatic cancers and characterization of genomic instability caused by MLH1 haploinsufficiency and complete deficiency
Study
EGAS00001000149
-
Glioblastoma_CRISPR_Screen
Study
EGAS00001001519
-
A comprehensive assessment of somatic mutation detection in cancer using whole genome sequencing
Study
EGAS00001001539
-
Whole genome sequencing of primary and metastatic Melanoma cases in an Australian cohort.
Study
EGAS00001001552
-
PSCP_mutation_analysis_in_hESCs
Study
EGAS00001001561
-
The_genetic_evolution_of_precursor_lesions_in_pancreatic_cancer
Study
EGAS00001001573
-
Integrated genomic analysis identifies driver genes and cisplatin-resistant progenitor phenotype in pediatric liver cancer
Study
EGAS00001005108
-
Whole-exome sequencing performed on a patient with chronic myelomonocytic leukemia and B cell acute lymphoblastic leukemia
Study
EGAS00001005117
-
Recapitulation of genetic predisposition to medulloblastoma in human neuroepithelial stem cells
Study
EGAS00001003620
-
In_Situ_Transcription_whole_genome_sequencing
Study
EGAS00001001971
-
FRCC_Exome_sequencing
Study
EGAS00001000176
-
Signatures of mismatch repair deficiency in cancer genomes
Study
EGAS00001000182
-
CML_blast_phase_rearrangement_screen
Study
EGAS00001000191
-
germline variants in children with hematological cancer
Study
EGAS00001006907
-
SCAT_osteosarcoma_sequencing
Study
EGAS00001000196
-
Non_Tumour_Renal_Cell_Line_Sequencing
Study
EGAS00001000205
-
MED12L Gene Alterations Define Aggressive BRCA2-Mutant Prostate Cancers
Study
EGAS00001001615
-
Accurate detection and classification of pediatric sarcomas based on cell-free DNA fragmentation patterns
Study
EGAS00001005127
-
Multiregional sequencing of IDH-WT glioblastoma reveals high genetic heterogeneity and a dynamic evolutionary history
Study
EGAS00001005128
-
Mutations conferring differential treatment response in breast cancer
Study
EGAS00001003626