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Whole exome sequencing of Finnish hereditary breast cancer families
Study
EGAS00001001835
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Genome-wide quantification of rare somatic mutations in normal human tissues using massively parallel sequencing
Study
EGAS00001001838
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The dataset of Southeast Borneo individuals (Banjar and Ngaju ethnic groups) was used as comparative data to determine the Asian parental population of the Malagasy. Our study found strong support for an origin of the Asian ancestry of Malagasy among the Banjar.
Study
EGAS00001001841
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Whole-genome sequencing of two probands with hereditary spastic paraplegia reveals novel splice-donor region mutation and known pathogenic mutation in SPG11
Study
EGAS00001001849
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Recurrent somatic JAK-STAT mutations within a novel RUNX1-mutated pedigree
Study
EGAS00001001862
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Summary statistics of meta-analysis using two genome-wide association study of inflammatory bowel disease in Koreans.
Study
EGAS00001005026
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A rare CTSC mutation in Papillon-Lefèvre Syndrome
Study
EGAS00001005040
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Recent genetic history of Denmark
Study
EGAS00001001868
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Exome and RNA sequencing of relapsed TCF3-PBX1 t(1;19) acute lymphoblastic leukemia
Study
EGAS00001001876
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Pediatric Papillary Thyroid Carcinoma Whole Exome Sequencing
Study
EGAS00001005187