Published July 2, 2025 | Version 0.1
Dataset Open

Summary Data from "Image-based, pooled phenotyping reveals multidimensional, disease-specific variant effects"

  • 1. EDMO icon University of Washington

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

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Additional details

Funding

National Institutes of Health
Center for the Multiplexed Assessment of Phenotype RM1HG010461
Chan Zuckerberg Initiative (United States)
CZIF2024-010284
Chan Zuckerberg Initiative (United States)
CP-2-1-Fowler

Software

Repository URL
https://github.com/FowlerLab/visseq
Programming language
Python
Development Status
Active