Policy to access RNAseq Patient Derived Sézary syndrome cells

Dr Lluís Espinosa
lespinosa@researchmar.net

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Dataset ID	Description	Technology	Samples
EGAD50000001646	We profile the whole-transcriptome (bulk RNAseq) of 7 patient-derived Sézary Syndrome (SS) cells to identify expression patterns, functional programs and expressed gene mutations that may provide clues on new therapeutic options for SS patients. The libraries were sequenced on NextSeq500 (Illumina) with a paired-end read length of 2x75bp. Raw data (FASTQ) and obtained processed data (VCF) including all called raw variants are available.	NextSeq 500	7