221 results for "study_type:"exome sequencing" AND repository:ega"
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WES for CNV-verified CTCs enriched by high-throughout microfluidic device from entire cancer patient leukopak
Study EGAS50000000724 -
Swedish Bipolar Disorder exome sequencing (SWEBIC)
Study EGAS00001005860 -
Diagnostic Exome Sequencing in Persons with Severe Intellectual Disability
Study EGAS00001000287 -
Exome sequencing identifies mutation of the ribosome in T-cell acute lymphoblastic leukemia
Study EGAS00001000296 -
Whole-exome study to identify the causative germline mutations of congenital macrothrombocytopenia
Study EGAS00001000371 -
Whole exome sequencing of virus-associated HCC
Study EGAS00001000389 -
A Cancer Cell-Line Titration Series for Evaluating Somatic Classification
Study EGAS00001001016 -
Comprehensive genomic characterization of early stage bladder cancer - whole exome sequencing data
Study EGAS50000000511 -
WES in muscle-invasive bladder cancer (MIBC) treated with durvalumab plus olaparib in the neoadjuvant setting: NEODURVARIB trial
Study EGAS50000000791 -
Novel de novo pathogenic variant in the GNAI1 as a cause of severe disorders of intellectual development with autistic features
Study EGAS00001005346 -
Multifocal ileal NETs study WES
Study EGAS00001004680
