-
Genomics_of_acral_lentiginous_melanoma___RNAseq
Study
EGAS00001003758
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Genetic Epidemiology of Chronic Lymphocytic Leukemia
Study
phs001568
-
Whole genome shotgun sequencing and somatic mutations data in Hepatocellular carcinoma
Study
EGAS00001002578
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Identification of genetic polymorphism on aggressive periodontitis
Study
JGAS000040
-
Identification of genetic polymorphism on aggressive periodontitis
Study
JGAS000024
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Foetal_phylogeny_8pcw___WGS_of_LCM_tissues
Study
EGAS00001004674
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Bulk paired RNAseq of CLL patients and HD donor T cells
Dataset
EGAD50000001368
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Exome sequencing of patient samples from study
Study
EGAS50000000171
-
Whole transcriptome seq from patient samples
Study
EGAS50000000172
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Novel compound heterozygous mutations in UHRF1 are associated with atypical immunodeficiency, centromeric instability, and facial anomalies (ICF) syndrome with distinctive genome-wide DNA hypomethylation
Study
JGAS000559