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Series GSE69735 Query DataSets for GSE69735
Status Public on Jun 12, 2016
Title Recurrent alterations of TNFAIP3 (A20) in T-cell large granular lymphocytic leukemia
Organism Homo sapiens
Experiment type Expression profiling by high throughput sequencing
Summary We identified a novel recurrent genetic lesion in T-LGL. Mutations of the tumour suppressor gene TNFAIP3 causing amino-acid exchanges or protein truncations were seen in 3/39 cases (8%).
Overall design RNA sequencing (Illumina HiSeq 2500) of 5 index patients with paired tumor and non-tumor samples.
Contributor(s) Klein-Hitpass L, Johansson P
Citation(s) 26199174
Submission date Jun 10, 2015
Last update date May 15, 2019
Contact name Ludger Klein-Hitpass
Phone +49 201 723 85552
Organization name Institut fuer Zellbiologie
Department Universitaetsklinikum
Lab BioChip Lab
Street address Virchowstr. 173
City Essen
ZIP/Postal code D-45122
Country Germany
Platforms (1)
GPL16791 Illumina HiSeq 2500 (Homo sapiens)
Samples (10)
GSM1707994 Patient1_N
GSM1707995 Patient1_T
GSM1707996 Patient2_N
BioProject PRJNA286292
SRA SRP059322

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE69735_Variant_analysis_duplicates_removed.txt.gz 3.5 Mb (ftp)(http) TXT
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Raw data are available in SRA
Processed data are available on Series record

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