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RUNX1 mutated families show phenotype heterogeneity and a somatic mutation profile unique to germline predisposed AML
Study
EGAS00001004273
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RNA-seq as a tool for evaluating human embryo competence
Study
EGAS00001003667
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High-resolution analyses of human sperm dynamic methylome reveals thousands of novel age-related epigenetic alterations
Study
EGAS00001004168
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Spatial_transcriptome_analysis_of_Paediatric_Thymus
Study
EGAS00001004281
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Coding and non-coding drivers of mantle cell lymphoma identified through exome and genome sequencing
Study
EGAS00001004289
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Circulating tumor cells for comprehensive and multiregional non-invasive genetic characterization of multiple myeloma (arrays set)
Study
EGAS00001004314
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Single-cell ATAC-seq analysis for COVID19 patients
Study
EGAS00001006559
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Overrepresentation of genetic variation in the AnkyrinG interactome is related to a range of neurological disorders
Study
EGAS00001004326
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Persistent STAG2 mutation in recurrent pediatric glioblastoma
Study
EGAS00001004340
-
Targeted sequencing DDR genes in cancer stem cells
Study
EGAS00001004892