Additional file 1 of scSNV-seq: high-throughput phenotyping of single nucleotide variants by coupled single-cell genotyping and transcriptomics

Cooper, Sarah E.; Coelho, Matthew A.; Strauss, Magdalena E.; Gontarczyk, Aleksander M.; Wu, Qianxin; Garnett, Mathew J.; Marioni, John C.; Bassett, Andrew R.

doi:10.6084/m9.figshare.25001673.v1

13059_2024_3169_MOESM1_ESM.pdf (2.24 MB)

Additional file 1 of scSNV-seq: high-throughput phenotyping of single nucleotide variants by coupled single-cell genotyping and transcriptomics

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posted on 2024-01-16, 05:00 authored by Sarah E. Cooper, Matthew A. Coelho, Magdalena E. Strauss, Aleksander M. Gontarczyk, Qianxin Wu, Mathew J. Garnett, John C. Marioni, Andrew R. Bassett

Additional file 1. Supplementary figures and text. Figs. S1, S2 and S3 and legends for Tables S1, S2 and S3.

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Single-cell CRISPR screen SNV GWAS Base editor Causal variant VUS

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Additional file 1 of scSNV-seq: high-throughput phenotyping of single nucleotide variants by coupled single-cell genotyping and transcriptomics

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