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Molecular_characterization_of_invasive_lobular_carcinoma
Study
EGAS00001000292
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A sequence-based genetic dissection of human immune cell types and implications for immune-related disease.
Study
EGAS00001000574
-
Assessing the impact of low frequency coding variants on disease risk using the Exomechip
Study
EGAS00001000584
-
Genome-wide SNP genotyping of Central African rainforest hunter-gatherers and neighbouring agriculturalists
Study
EGAS00001000605
-
JMML targeted sequencing (2013)
Study
EGAS00001001324
-
The molecular landscape of colorectal cancer (17 cases)
Study
EGAS00001002174
-
Osteosarcoma_RNAseq
Study
EGAS00001000615
-
BLUEPRINT ChIP-seq data for cells in the haematopoietic lineages, from adult and cord blood samples.
Study
EGAS00001000326
-
Genome_Diversity_in_Africa_Project___GemCode_libraries
Study
EGAS00001001589
-
H3Africa - An integrated approach to the identification of genetic determinants of susceptibility to trypanosomiasis
Study
EGAS00001007173
-
Sequencing of heritable Bleeding and Platelet Disorders
Study
EGAS00001001172
-
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
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Bacterial SNPs in the human gut microbiome associate with host BMI
Study
EGAS00001007204
-
MED12L Gene Alterations Define Aggressive BRCA2-Mutant Prostate Cancers
Study
EGAS00001001615
-
Identification_of_rare_variants_associated_with_cardiovascular_traits_in_Cilento_isolates
Study
EGAS00001000620
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Rare SNPs in receptor tyrosine kinases are negative outcome predictors in multiple myeloma
Study
EGAS00001001665
-
Breast_Cancer_Matched_Pair_Cell_Line_Whole_Genomes
Study
EGAS00001000166
-
Adenoma to Carcinoma transition in Colorectal Cancer
Study
EGAS00001003468
-
Illumina ExomeChip genotyping data from the Cretan Greek isolate collection HELIC MANOLIS
Study
EGAS00001000630
-
Combination_therapies_for_personalized_cancer_medicine
Study
EGAS00001000655
-
BASIS_RNAseq
Study
EGAS00001000707
-
Biallelic DICER1 mutations in sporadic pleuropulmonary blastoma
Study
EGAS00001000662
-
Fixation effects on variant-calling in a clinical resequencing panel
Study
EGAS00001003507
-
PAGE: Prenatal Assessment of Genomes and Exomes
Study
EGAS00001001713
-
Exome sequencing of uterine leiomyosarcomas
Study
EGAS00001001612