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Status |
Public on Mar 09, 2023 |
Title |
CRISPR screens identify gene targets at breast cancer risk loci [RNA-seq] |
Organism |
Homo sapiens |
Experiment type |
Expression profiling by high throughput sequencing
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Summary |
Genome-wide association studies (GWAS) have identified >200 loci associated with breast cancer (BC) risk. The majority of candidate causal variants (CCVs) are in non-coding regions and likely modulate cancer risk by regulating gene expression. However, pinpointing the exact target of the association, and identifying the phenotype it mediates, is a major challenge in the interpretation and translation of GWAS.
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Overall design |
Transcriptome, open chromatin, and chromatin interaction profiling using RNA-seq, ATAC-seq and H3K27ac-mediated HiChIP of six immortalized mammary epithelial cell lines representing breast cells with either a luminal progenitor signature (K5+/K19+, K5+/K19-), a mesenchymal signature (B80-T17, mesHMLE) or a more epithelial like signature (B80-T5, HMLE)
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Contributor(s) |
Beesley J |
Citation(s) |
36991492 |
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Submission date |
Dec 01, 2022 |
Last update date |
Jun 08, 2023 |
Contact name |
Jonathan Beesley |
E-mail(s) |
jonathan.beesley@qimrberghofer.edu.au
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Organization name |
QIMR Berghofer
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Street address |
300 Herston Rd Herston
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City |
Brisbane |
State/province |
QLD |
ZIP/Postal code |
4006 |
Country |
Australia |
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Platforms (1) |
GPL16791 |
Illumina HiSeq 2500 (Homo sapiens) |
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Samples (12)
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This SubSeries is part of SuperSeries: |
GSE219168 |
CRISPR screens identify gene targets at breast cancer risk loci |
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Relations |
BioProject |
PRJNA907298 |