Summary Data from "Image-based, pooled phenotyping reveals multidimensional, disease-specific variant effects"
Description
Variant in situ Sequencing (VIS-seq) is a platform for optically profiling thousands of transgenically expressed protein-coding variants simultaneously. VIS-seq comprises a cassette with a promoter expressing a circular RNA containing one or more barcodes that are sequenced in situ to reveal the identity of the variant expressed in each cell and a second promoter expressing the protein variant. We used VIS-seq to create morphological profiles comprising a large set of measurements of the intensity, distribution and shape of different markers for >3,000 variants of lamin A and PTEN from ~11.4 million cell images. Lamin A variants were expressed in U2OS cells and PTEN variants in either iPS cells or derived neurons. VIS-seq variant profiles may be explored at visseq.gs.washington.edu.
Files
VISseq_summarydata_v0.1.zip
Files
(1.3 GB)
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md5:34a464c6d79697443ace5809b0327086
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Additional details
Funding
Software
- Repository URL
- https://github.com/FowlerLab/visseq
- Programming language
- Python
- Development Status
- Active