-
Neuroblastoma tumor heterogeneity and cell plasticity (from PDX and cell lines)
Study
EGAS00001004781
-
Neuroblastoma tumor heterogeneity and cell plasticity (from patients)
Study
EGAS00001005322
-
Dataset that contains runs of submission 2
Dataset
EGAD50000000436
-
Dataset that contains runs of submission 5
Dataset
EGAD50000000440
-
Dataset that contains runs of submission 1
Dataset
EGAD50000000448
-
Submission 17 - study_title 2
Study
EGAS50000000022
-
Submission 13 - study_title 2
Study
EGAS50000000020
-
dat
Dataset
EGAD50000000001
-
Submission 1 - study_title 2
Study
EGAS50000000460
-
Submission 9 - study_title 2
Study
EGAS50000000432
-
Dataset that contains runs of submission 10
Dataset
EGAD50000000424
-
Whole exome sequencing of Dutch Parkinson disease patients
Dataset
EGAD00001002773
-
Genetics of gene expression in primary human immune cells Data Access Committee
Dac
EGAC01000000009
-
HipSci_RNASEQ_Kabuki
Study
EGAS00001001989
-
Native_American_Ancient_DNA_sequencing
Study
EGAS00001001802
-
HipSci_RNASEQ_Congenital_hyperinsulinia
Study
EGAS00001001988
-
Resolving_the_Genetic_Architecture_of_Aseptic_Loosening_After_Total_Hip_Replacement
Study
EGAS00001001883
-
The molecular landscape of colorectal cancer reveals genetic mutations.
Study
EGAS00001001893
-
The_contribution_of_POT1_variants_to_sporadic_melanoma_development
Study
EGAS00001001964
-
HipSci_RNASEQ_Battens
Study
EGAS00001001987
-
HipSci___Whole_Exome_sequencing___Battens
Study
EGAS00001001975
-
HipSci___Whole_Exome_sequencing___BPD
Study
EGAS00001001976
-
HipSci___Whole_Exome_sequencing___Congenital_hyperinsulinia
Study
EGAS00001001977
-
HipSci___Whole_Exome_sequencing___Ataxia
Study
EGAS00001001978
-
HipSci___Whole_Exome_sequencing___HSP
Study
EGAS00001001979
-
HipSci___Whole_Exome_sequencing___Kabuki
Study
EGAS00001001981
-
HipSci___Whole_Exome_sequencing___Macular_dystrophy
Study
EGAS00001001982
-
HipSci___Whole_Exome_sequencing___PID
Study
EGAS00001001983
-
HipSci___Whole_Exome_sequencing___Retinitis_Pigmentosa
Study
EGAS00001001984
-
HipSci_RNASEQ_Alport
Study
EGAS00001001986
-
HipSci_RNASEQ_Spastic_paraplegia
Study
EGAS00001001991
-
HipSci_RNASEQ_Ataxia
Study
EGAS00001001992
-
HipSci_RNASEQ_BPD
Study
EGAS00001001993
-
HipSci_RNASEQ_Hypertrophic_Cardiomyopathy
Study
EGAS00001001994
-
HipSci_RNASEQ_Macular_Dystrophy
Study
EGAS00001001995
-
HipSci_RNASEQ_Retinitis_Pigmentosa
Study
EGAS00001001996
-
HipSci_RNASEQ_Usher syndrome and congenital eye defects
Study
EGAS00001001997
-
HipSci HumanExome BeadChip analysis - Alport Syndrome
Study
EGAS00001002009
-
HipSci HumanExome BeadChip analysis - Congenital Hyperinsulinia
Study
EGAS00001002010
-
HipSci HumanExome BeadChip analysis - Hypertrophic Cardiomyopathy
Study
EGAS00001002011
-
HipSci HumanExome BeadChip analysis - Primary immune deficiency
Study
EGAS00001002012
-
HipSci HumanExome BeadChip analysis - Bleeding and Platelet disorders
Study
EGAS00001002013
-
HipSci HumanExome BeadChip analysis - Retinitis Pigmentosa
Study
EGAS00001002015
-
HipSci HumanExome BeadChip analysis - Battens disease
Study
EGAS00001002016
-
HipSci HumanHT 12 Expression BeadChip analysis - Hereditary Cerebellar Ataxias
Study
EGAS00001002020
-
HipSci HumanHT 12 Expression BeadChip analysis - Kabuki syndrome
Study
EGAS00001002022
-
HipSci HumanHT 12 Expression BeadChip analysis - Usher syndrome and congenital eye defects
Study
EGAS00001002023
-
HipSci HumanHT 12 Expression BeadChip analysis - Alport syndrome
Study
EGAS00001002024
-
HipSci HumanHT 12 Expression BeadChip analysis - Congenital Hyperinsulinia
Study
EGAS00001002025
-
HipSci HumanHT 12 Expression BeadChip analysis - Hypertrophic Cardiomyopathy
Study
EGAS00001002026