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Exploration of CNV’s and SNV’s in cancers with well-known genetic rearrangements: Identification of additional genetic changes in rearrangements-driven cancer
Study
EGAS00001000673
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Genotyping_of_additional_Inflammatory_Bowel_Disease_cases___2014
Study
EGAS00001000924
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Papuan_Genotyping
Study
EGAS00001001587
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Analysis of a cohort of familial ademomatous polyposis patients bearing APC gene mutation
Study
EGAS00001007237
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Copy number analysis of Diamond-Blackfan Anemia (DBA) using SNP array
Study
EGAS00000000105
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WES in HCCOs with varying Doxorubicin resistance
Study
EGAS50000000043
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Genotype and exome data for an Australian Aboriginal population: a reference panel for health-based research
Study
EGAS00001001585
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Genomic analysis and evolutionary modeling of breast and larynx cancer, based on specimens from Polish population
Study
EGAS00001006456
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Proteogenomic analysis reveals RNA as a source for tumor-agnostic neoantigen identification (H021)
Study
EGAS00001006706
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Genomic catastrophes frequently arise in esophageal adenocarcinoma and drive tumorigenesis.
Study
EGAS00001000750