-
Genetic characterization of B-cell prolymphocytic leukemia: a hierarchical prognostic model involving MYC and TP53 abnormalities - WXS
Study
EGAS00001003275
-
Pancreatic cancer organoids recapitulate disease and allow personalized drug screening
Study
EGAS00001003369
-
Fixation effects on variant-calling in a clinical resequencing panel
Study
EGAS00001003507
-
MutWP1__CRUK_Grand_Challenge_Mutographs_of_Cancer__Colorectal_LCM
Study
EGAS00001003455
-
Whole exome sequencing of 49 tumor-blood pairs and transcriptome sequencing of 44 tumors for adrenocortical tumors
Study
EGAS00001000712
-
Autozygosity_pilot___QMUL
Study
EGAS00001000717
-
Assessment_of_epigenetic_variation_in_human_iPS_cells_Medip
Study
EGAS00001000741
-
Integrative_genome_profiling_in_AML
Study
EGAS00001000858
-
The_life_history_of_colorectal_cancer_metastases_study_WGS_X10
Study
EGAS00001000864
-
HipSci_Illumina 450K Methylation analysis_Healthy volunteers
Study
EGAS00001000865
-
HipSci HumanHT_12v4 Expression BeadChip analysis-Healthy volunteers
Study
EGAS00001000867
-
Succession Of Transiently Active Tumour-Initiating Cell Clones inHuman Pancreatic Cancer
Study
EGAS00001000882
-
Metastatic_Breast_Cancer_Whole_Genome
Study
EGAS00001000902
-
DKFZ-HIPO Project H021/NCT MASTER
Study
EGAS00001000948
-
Barcelona_kids_with_melanoma
Study
EGAS00001000733
-
ESGI_Exome_sequencing_in_Circulating_Tumor_Cells_to_determine_therapy_related_markers_____
Study
EGAS00001000747
-
MYD88/TLR mutations in CLL
Study
EGAS00001000772
-
Genetic_profiling_of_mucosal_melanoma
Study
EGAS00001001115
-
ESGI___Whole_Genome_Sequencing_of_samples_from_the_INGI_Val_Borbera_genetic_isolate__X10_
Study
EGAS00001001123
-
Congenital_anosmia_1
Study
EGAS00001001124
-
DPY30_ChIP_seq
Study
EGAS00001001132
-
HipSci___Whole_Exome_sequencing___Monogenic_Diabetes
Study
EGAS00001001140
-
Guardians_of_the_genome__protecting_DNA_from_endogenous_sources_of_damage_
Study
EGAS00001000800
-
Illumina HumanCoreExome genotyping data from the British Society for Surgery of the Hand Genetics of Dupuytren’s Disease consortium (BSSH-GODD consortium) collection
Study
EGAS00001001206
-
Genetic_screening__of_GPI_anchor_protein_synthesis__
Study
EGAS00001001256
-
Guardians_of_the_genome__protecting_DNA_from_endogenous_sources_of_damage_
Study
EGAS00001000874
-
HipSci Illumina 450K Methylation analysis-Rare_BBS
Study
EGAS00001001274
-
HipSci HumanExome BeadChip analysis-Rare_BBS
Study
EGAS00001001272
-
HipSci HumanHT 12v4 Expression BeadChip analysis - monogenic diabetes
Study
EGAS00001001277
-
The_genetic_evolution_of_precursor_lesions_in_pancreatic_cancer
Study
EGAS00001001573
-
Mechanisms_of_patient_response_to_Dabrafenib_in_Melanoma
Study
EGAS00001000946
-
Somatic_Genetics_of_lesions_from_a_POT1_patient
Study
EGAS00001001343
-
TGS___Comprehensive_Molecular_Characterization_of_Colorectal_Cancer_Metastases__MOSAIC_
Study
EGAS00001000958
-
HipSci___Whole_Exome_sequencing___Bardet_Biedl_Syndrome
Study
EGAS00001000969
-
Genetic landscape of relapsed DLBCL
Study
EGAS00001001553
-
PSCP_mutation_analysis_in_hESCs
Study
EGAS00001001561
-
PSCP_bisulphite_analysis_in_hESCs
Study
EGAS00001001625
-
RNA_seq_analysis_of_transcriptome_variation_with_human_ESC_subclones
Study
EGAS00001001655
-
Investigating_the_genetics_of_immunity_against_Salmonella_in_humans
Study
EGAS00001001664
-
HipSci___RNAseq___Rare_Monogenic Diabetese
Study
EGAS00001001137
-
HipSci RNA sequencing for embryonic stem cell control lines
Study
EGAS00001001727
-
ENU_CCK_81_cetuximab_pilot_project
Study
EGAS00001001743
-
HipSci whole exome sequencing for embryonic stem cell control lines
Study
EGAS00001001726
-
HipSci genotyping microarray for embryonic stem cell control lines
Study
EGAS00001001730
-
ENU_NCI_H508_Cetuximab_SecondRound
Study
EGAS00001001745
-
Genome_Diversity_in_Africa_Project___ancient_samples___standard_libraries
Study
EGAS00001001182
-
Onco-exaptation of an Endogenous Retroviral LTR Drives IRF5 Expression in Hodgkin Lymphoma
Study
EGAS00001001205
-
HipSci HumanHT 12v4 Expression BeadChip analysis-Rare_BBS
Study
EGAS00001001276
-
HipSci___RNAseq___Rare_BBS
Study
EGAS00001001318
-
HipSci - Human Induced Pluripotent Stem Cells Initiative
Study
EGAS00001001465