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UK10K NEURO ABERDEEN
Study
EGAS00001000109
-
Whole-Genome Sequencing Suggests Schizophrenia Risk Mechanisms in Humans with 22q11.2 Deletion Syndrome
Study
EGAS00001002344
-
UK10K_RARE_NEUROMUSCULAR
Study
EGAS00001000101
-
UK10K_RARE_FIND
Study
EGAS00001000128
-
UK10K_RARE_CILIOPATHIES
Study
EGAS00001000126
-
UK10K_RARE_SIR
Study
EGAS00001000130
-
UK10K RARE CHD
Study
EGAS00001000125
-
UK10K OBESITY TWINSUK
Study
EGAS00001000306
-
The Prediction and Prevention of Preeclampsia
Study
EGAS00001001898
-
The Immune Microenvironment, Genome–Wide Copy Number Aberrations and Survival in Mesothelioma
Study
EGAS00001002323
-
Genome wide association study on coronary heart disease in patients with familial hypercholesterolemia
Study
EGAS00001000734
-
Development of targeted DNA sequencing panel for brain tumors
Study
EGAS50000000699
-
Epigenetic profiling of primary human thymocyte subsets
Study
EGAS50000001106
-
ChIP sequencing for β-catenin and histone modifications in HCC cell lines and organoids with CTNNB1 mutations
Study
EGAS50000001274
-
Acute_Lymphoblastic_Leukemia_Exome_sequencing_2_
Study
EGAS00001000200
-
Mapping and phasing of structural variation in patient genomes using nanopore sequencing
Study
EGAS00001002333
-
Acute_Lymphoblastic_Leukemia_Exome_sequencing
Study
EGAS00001000201
-
Myeloproliferative_Disorder_Sequencing
Study
EGAS00001000198
-
Myeloproliferative_Disorder_Sequencing
Study
EGAS00001000199
-
Celiac disease meta-analysis
Study
EGAS00001003805
-
Acute_Lymphoblastic_Leukemia_Sequencing
Study
EGAS00001000058
-
We screened 2.5 million SNPs in 161 individuals from 13 Sahelian populations from Western, Central and Eastern parts of the belt, and including both nomadic and sedentary groups
Study
EGAS00001001610
-
Biological insights from the whole genome sequences of human embryonic stem cell lines
Study
EGAS00001002400
-
Genomic History of the Solomon Islands
Study
EGAS00001006116
-
Korea4K: whole genome sequences of 4,157 Koreans with 107 phenotypes derived from extensive health check-ups
Study
EGAS00001007580