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Quantification of chromosomal copy number aberrations by shallow whole-genome sequencing
Study
EGAS00001000642
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These are from Korean HCC samples with exome sequencing
Study
EGAS00001000604
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Search for new loci and low-frequency variants influencing glioma risk by exome-array analysis
Study
EGAS00001001258
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Robust methylation-based classification of brain tumours using nanopore sequencing
Study
EGAS00001006540
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Oncogenic fate conversion by PRDM16s causes acute myeloid leukemia
Study
EGAS00001003235
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Healthspan and lifespan extension by fecal microbiota transplantation in progeroid mice
Study
EGAS00001003656
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Neoadjuvant immunotherapy leads to pathological responses in MMR proficient and MMR deficient early stage colon cancers
Study
EGAS00001004160
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Non-viral precision T cell receptor replacement for personalized cell therapy
Study
EGAS00001006898
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CINECA_synthetic_cohort_EUROPE_UK1 referencing fake samples
Dataset
EGAD00001006673
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Human genomic and phenotypic synthetic data for the study of rare diseases
Study
EGAS00001005702