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Series GSE240212 Query DataSets for GSE240212
Status Public on Jul 02, 2024
Title Spatial Transcriptomics reveals that cells that experience intratumoral hypoxia retain hypoxia-associated transcriptional programs after invading into oxygenated tumor regions.
Organism Homo sapiens
Experiment type Other
Summary To understand the role of hypoxia in metastatic progression, we sought to spatially map gene expression in hypoxic cells compared with cells that migrated to oxygenated tumor regions. We adapted the Visium spatial transcriptomics protocol to perform concurrent transcriptional profiling and fluorescent imaging of our hypoxia fate-mapping system.
 
Overall design Hypoxia fate-mapping MDA-MB-231 tumors (Godet et. al, 2019) were harvested 18 days post-implantation and immediately frozen in clear OCT. 10 μm tumor slices were placed within the fiducial frame of the Visium slide. The tissue was pre-fixed in cold methanol and imaged at 10X magnification using a Cytation5 in the RFP and GFP channels to acquire native fluorescence. The slide was immediately transferred to cold methanol with DAPI. DAPI staining was imaged at 10X using Cytation5.
 
Contributor(s) Godet I, Gilkes D
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Submission date Aug 07, 2023
Last update date Jul 03, 2024
Contact name Ines Godet
Organization name Johns Hopkins University
Department Oncology
Lab Gilkes
Street address 1650 Orleans Street, CRB1, room 128
City Baltimore
State/province MD
ZIP/Postal code 21231
Country USA
 
Platforms (1)
GPL24676 Illumina NovaSeq 6000 (Homo sapiens)
Samples (2)
GSM7688224 Tumor-897
GSM7688225 Tumor-899
Relations
BioProject PRJNA1002980

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Supplementary file Size Download File type/resource
GSE240212_RAW.tar 110.1 Mb (http)(custom) TAR (of CSV, JPG, JSON, MTX, PNG, TSV)
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Raw data are available in SRA
Processed data provided as supplementary file

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