Deciphering novel TCF4-driven mechanisms underlying a common triplet repeat expansion-mediated disease
short and long read data generated from cultured corneal endothelial cells (CECs) of unaffected controls, expansion positive Fuchs Endothelial Corneal Dystrophy (FECD) and expansion negative FECD individuals.
- Type: RNASeq
- Archiver: European Genome-Phenome Archive (EGA)
Click on a Dataset ID in the table below to learn more, and to find out who to contact about access to these data
Dataset ID | Description | Technology | Samples |
---|---|---|---|
EGAD50000000435 | Sequel | 9 | |
EGAD50000000436 | Illumina HiSeq 4000 | 10 |
Publications | Citations |
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Deciphering novel TCF4-driven mechanisms underlying a common triplet repeat expansion-mediated disease.
PLoS Genet 20: 2024 e1011230 |
1 |