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RNAseq_of_Human_Organoid_Lines
Study
EGAS00001003888
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DNA methylomes of monozygotic twins clinically discordant for multiple sclerosis
Study
EGAS00001003147
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DNA methylation atlas of normal human cell types
Study
EGAS00001006791
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Germline SDHB-inactivating mutation in gastric spindle cell sarcoma (HIPO-021)
Study
EGAS00001004277
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Analysis of exonic somatic variants in light-chain amyloidosis (ALA) and ALA concomitant with multiple myeloma
Study
EGAS00001004214
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Mutator phenotype and specific mutational signature explain an increased risk of hematological malignancies in patients with Xeroderma Pigmentosum
Study
EGAS00001004511
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Exome sequencing of HCV+ lymphoma
Study
EGAS00001006860
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Atypical teratoid/rhabdoid tumoroids reveal subgroup-specific drug vulnerabilities WGS
Study
EGAS00001006865
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Epigenetics/genetics of the patient-derived xenografts of pediatric T-cell leukemia
Study
EGAS00001003248
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Super enhancers define regulatory subtypes and cell identity in neuroblastoma - RNA-seq
Study
EGAS00001004552