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José L. McFaline-Figueroa

Researcher at University of Washington

Publications -  34
Citations -  2730

José L. McFaline-Figueroa is an academic researcher from University of Washington. The author has contributed to research in topics: Biology & Medicine. The author has an hindex of 16, co-authored 25 publications receiving 1621 citations. Previous affiliations of José L. McFaline-Figueroa include Massachusetts Institute of Technology.

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Joint profiling of chromatin accessibility and gene expression in thousands of single cells

TL;DR: By applying sci-CAR to lung adenocarcinoma cells and mouse kidney tissue, the authors demonstrate precision in assessing expression and genome accessibility at a genome-wide scale and provide an improvement over bulk analysis, which can be confounded by differing cellular subgroups.
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Cicero Predicts cis-Regulatory DNA Interactions from Single-Cell Chromatin Accessibility Data.

TL;DR: Cicero is introduced, an algorithm that identifies co-accessible pairs of DNA elements using single-cell chromatin accessibility data and so connects regulatory elements to their putative target genes and is applied to investigate how dynamically accessible elements orchestrate gene regulation in differentiating myoblasts.
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A Genome-wide Framework for Mapping Gene Regulation via Cellular Genetic Screens.

TL;DR: A multiplex, expression quantitative trait locus (eQTL)-inspired framework for mapping enhancer-gene pairs by introducing random combinations of CRISPR/Cas9-mediated perturbations to each of many cells, followed by single-cell RNA sequencing (RNA-seq).
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Dynamics of Gene Expression in Single Root Cells of Arabidopsis thaliana

TL;DR: The results demonstrate that single cell transcriptomics holds promise for studying plant development and plant physiology with unprecedented resolution and address the longstanding question of possible heterogeneity among cell types in the response to an abiotic stress.
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Massively multiplex chemical transcriptomics at single-cell resolution

TL;DR: The results with histone deacetylase inhibitors support the view that chromatin acts as an important reservoir of acetate in cancer cells, and reveal substantial intercellular heterogeneity in response to specific compounds, commonalities inresponse to families of compounds, and insight into differential properties within families.