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Marmar Moussa

Researcher at University of Connecticut

Publications -  23
Citations -  414

Marmar Moussa is an academic researcher from University of Connecticut. The author has contributed to research in topics: Imputation (statistics) & Interactive visualization. The author has an hindex of 5, co-authored 19 publications receiving 153 citations.

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Comparative cellular analysis of motor cortex in human, marmoset and mouse

Trygve E. Bakken, +121 more
- 01 Oct 2021 - 
TL;DR: The primary motor cortex (M1) is essential for voluntary fine-motor control and is functionally conserved across mammals using high-throughput transcriptomic and epigenomic profiling of more than 450k single nuclei in humans, marmoset monkeys and mice as mentioned in this paper.
Posted ContentDOI

Evolution of cellular diversity in primary motor cortex of human, marmoset monkey, and mouse

Trygve E. Bakken, +102 more
- 01 Apr 2020 - 
TL;DR: The primary motor cortex (M1) is essential for voluntary fine motor control and is functionally conserved across mammals, and a broadly conserved cellular makeup is demonstrated, whose similarity mirrors evolutionary distance and is consistent between the transcriptome and epigenome.
Journal ArticleDOI

Single cell RNA-seq data clustering using TF-IDF based methods

TL;DR: Novel computational approaches for clustering scRNA-seq data based on the Term Frequency - Inverse Document Frequency (TF-IDF) transformation that has been successfully used in the field of text analysis are presented.
Journal ArticleDOI

Locality Sensitive Imputation for Single Cell RNA-Seq Data.

TL;DR: This article studies some existing single cell RNA sequencing imputation methods and proposes a novel iterative imputation approach based on efficiently computing highly similar cells and presents the results of a comprehensive assessment of existing and proposed methods on real scRNA-Seq data sets with varying per cell sequencing depth.
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An unbiased approach to defining bona fide cancer neoepitopes that elicit immune-mediated cancer rejection.

TL;DR: T cells elicited by the active neoepitopes identified here demonstrated a stem-like early dysfunctional phenotype associated with effective responses against viruses and tumors of transgenic mice, which can be exploited for generation of personalized human cancer vaccines.