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Transcriptome analysis of CDAN1 deficiency in human erythroleukemic K562 cells.

GSE225925 Homo sapiens Expression profiling by high throughput sequencing 6 samples Submitted 2024/06/30 Platform GPL24676
Summary
Congenital dyserythropoietic anemia Type 1 (CDA1) is a rare macrocytic anemia caused by loss-of-function mutation of CDAN1. To investigate the functional role of CDAN1, we performed RNA-sequencing on human erythroleukemic K562 cells with CDAN1 shRNA knockdown using a doxycycline inducible system
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Direct links to NCBI, no account and no request form: the whole study as GSE225925_RAW.tar, processed values as the series matrix, the supplementary file directory, and per-sample supplementary files for any of the 6 samples. Raw sequencing reads are also available from ENA.

Also filed as BioProject PRJNA938051 and SRA study SRP424121. Searching any of these in the dataset finder brings you back here.

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