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1.
Cell Syst ; 15(5): 462-474.e5, 2024 May 15.
Article in English | MEDLINE | ID: mdl-38754366

ABSTRACT

Single-cell expression dynamics, from differentiation trajectories or RNA velocity, have the potential to reveal causal links between transcription factors (TFs) and their target genes in gene regulatory networks (GRNs). However, existing methods either overlook these expression dynamics or necessitate that cells be ordered along a linear pseudotemporal axis, which is incompatible with branching trajectories. We introduce Velorama, an approach to causal GRN inference that represents single-cell differentiation dynamics as a directed acyclic graph of cells, constructed from pseudotime or RNA velocity measurements. Additionally, Velorama enables the estimation of the speed at which TFs influence target genes. Applying Velorama, we uncover evidence that the speed of a TF's interactions is tied to its regulatory function. For human corticogenesis, we find that slow TFs are linked to gliomas, while fast TFs are associated with neuropsychiatric diseases. We expect Velorama to become a critical part of the RNA velocity toolkit for investigating the causal drivers of differentiation and disease.


Subject(s)
Cell Differentiation , Gene Regulatory Networks , RNA , Transcription Factors , Humans , Transcription Factors/genetics , Transcription Factors/metabolism , Gene Regulatory Networks/genetics , Cell Differentiation/genetics , RNA/genetics , RNA/metabolism , Single-Cell Analysis/methods , Gene Expression Regulation/genetics
2.
Science ; 380(6643): eabn5856, 2023 04 28.
Article in English | MEDLINE | ID: mdl-37104572

ABSTRACT

Species persistence can be influenced by the amount, type, and distribution of diversity across the genome, suggesting a potential relationship between historical demography and resilience. In this study, we surveyed genetic variation across single genomes of 240 mammals that compose the Zoonomia alignment to evaluate how historical effective population size (Ne) affects heterozygosity and deleterious genetic load and how these factors may contribute to extinction risk. We find that species with smaller historical Ne carry a proportionally larger burden of deleterious alleles owing to long-term accumulation and fixation of genetic load and have a higher risk of extinction. This suggests that historical demography can inform contemporary resilience. Models that included genomic data were predictive of species' conservation status, suggesting that, in the absence of adequate census or ecological data, genomic information may provide an initial risk assessment.


Subject(s)
Eutheria , Extinction, Biological , Genetic Variation , Animals , Female , Pregnancy , Eutheria/genetics , Genome , Population Density , Risk
3.
Pac Symp Biocomput ; 26: 131-142, 2021.
Article in English | MEDLINE | ID: mdl-33691011

ABSTRACT

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), a close relative of SARS-CoV-1, causes coronavirus disease 2019 (COVID-19), which, at the time of writing, has spread to over 19.9 million people worldwide. In this work, we aim to discover drugs capable of inhibiting SARS-CoV-2 through interaction modeling and statistical methods. Currently, many drug discovery approaches follow the typical protein structure-function paradigm, designing drugs to bind to fixed three-dimensional structures. However, in recent years such approaches have failed to address drug resistance and limit the set of possible drug targets and candidates. For these reasons we instead focus on targeting protein regions that lack a stable structure, known as intrinsically disordered regions (IDRs). Such regions are essential to numerous biological pathways that contribute to the virulence of various viruses. In this work, we discover eleven new SARS-CoV-2 drug candidates targeting IDRs and provide further evidence for the involvement of IDRs in viral processes such as enzymatic peptide cleavage while demonstrating the efficacy of our unique docking approach.


Subject(s)
COVID-19 , SARS-CoV-2 , Computational Biology , Drug Discovery , Humans
4.
Pac Symp Biocomput ; 26: 328-335, 2021.
Article in English | MEDLINE | ID: mdl-33691029

ABSTRACT

While the coronavirus pandemic has affected all demographic brackets and geographies, certain areas have been more adversely affected than others. This paper focuses on Veterans as a potentially vulnerable group that might be systematically more exposed to infection than others because of their co-morbidities, i.e., greater incidence of physical and mental health challenges. Using data on 122 Veteran Healthcare Systems (HCS), this paper tests three machine learning models for predictive analysis. The combined LASSO and ridge regression with five-fold cross validation performs the best. We find that socio-demographic features are highly predictive of both cases and deaths-even more important than any hospital-specific characteristics. These results suggest that socio-demographic and social capital characteristics are important determinants of public health outcomes, especially for vulnerable groups, like Veterans, and they should be investigated further.


Subject(s)
COVID-19 , Artificial Intelligence , Computational Biology , Demography , Humans , SARS-CoV-2
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