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Evan Murray

Researcher at Broad Institute

Publications -  30
Citations -  2516

Evan Murray is an academic researcher from Broad Institute. The author has contributed to research in topics: Biology & Gene. The author has an hindex of 7, co-authored 14 publications receiving 841 citations. Previous affiliations of Evan Murray include Harvard University.

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Slide-seq: A scalable technology for measuring genome-wide expression at high spatial resolution

TL;DR: Slide-seq provides a scalable method for obtaining spatially resolved gene expression data at resolutions comparable to the sizes of individual cells, and defines the temporal evolution of cell type–specific responses in a mouse model of traumatic brain injury.
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Highly sensitive spatial transcriptomics at near-cellular resolution with Slide-seqV2.

TL;DR: Slide-seqV2, a technology that enables transcriptome-wide detection of RNAs with a spatial resolution of 10 μm, is reported, which combines improvements in library generation, bead synthesis and array indexing to reach an RNA capture efficiency ~50% that of single-cell RNA-seq data (~10-fold greater than Slide-seq).
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Robust decomposition of cell type mixtures in spatial transcriptomics

TL;DR: In this paper, the authors propose robust cell type decomposition (RCTD) to detect mixtures and identify cell types on simulated datasets, which can accurately reproduce known cell type and subtype localization patterns in Slide-seq and Visium datasets.
Posted ContentDOI

Robust decomposition of cell type mixtures in spatial transcriptomics

TL;DR: Robust Cell Type Decomposition (RCTD) is developed, a computational method that leverages cell type profiles learned from single-cell RNA sequencing data to decompose mixtures, such as those observed in spatial transcriptomic technologies.
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In situ genome sequencing resolves DNA sequence and structure in intact biological samples

TL;DR: In situ genome sequencing (IGS) as discussed by the authors is a method for simultaneously sequencing and imaging genomes within intact biological samples, which can directly connect sequence and structure across length scales from single base pairs to whole organisms.