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Biology subjects

Honkala, A.

Publications and source records attributed to Honkala, A..

3 recordsLinked to original sources

Python Encoders for Archetypal Convex Hulls (PEACH): PyTorch-Based Archetypal Analysis

Samples of closely related cells often contain substantial cell state heterogeneity, which traditional clustering-based analyses struggle to de-convolve. Archetype analysis is an alternative analysis approach that identifies a minimal convex hull enclosing all data points in a dimensionally-reduced space, such as PCA space. The points of this convex manifold, or hull, each represent theoretical extremal states specialized in a subset of functions that are mutually exclusive to the extremal states found at each other vertex. The transition between two points represents a Pareto front of tradeoffs between potential cell states. Cell distances from each archetype and direction between archetypes then carry interpretable biological information revealing features of resource tradeoffs in cell state regulation. The archetypal points themselves are theoretical pure extremal states rarely accessed by real cells, which instead display a combination of archetype weights/mixture coefficients representing a mixture of specializations. By characterizing the relationships between gene expression and archetype distance, archetypal analysis can identify the phenotypic features of theoretically pure specialist states, the phenotypic tradeoffs of real cells, and the boundaries of accessible cell states in the analyzed sample. Here we present Python Encoders for Archetypal Convex Hulls (PEACH), a new PyTorch-based archetype analysis package compatible with the scVerse ecosystem that recapitulates and extends features available in previous archetype analysis packages. This includes a hyperparameter search function to identify the best k archetypes that fit an input dataset. PEACH uses a deliberately constrained autoencoder architecture to directly learn an archetypal latent space, replacing previous alternating least squares methods with a highly performant, GPU-accelerated archetype analysis method that is scalable to modern scRNAseq datasets of hundreds of thousands of cells. Crucially, PEACH includes automated hyperparameter search with cross-validation to identify optimal archetype and initialization configurations, enabling users to implement archetype analysis without extensive manual hyperparameter optimization and testing.

systems biology↗

Longitudinal profiling of the microbiome at four body sites reveals core stability and individualized dynamics during health and disease

To understand dynamic interplay between the human microbiome and host during health and disease, we analyzed the microbial composition, temporal dynamics, and associations with host multi-omics, immune and clinical markers of microbiomes from four body sites in 86 participants over six years. We found that microbiome stability and individuality are body-site-specific and heavily influenced by the host. The stool and oral microbiome were more stable than the skin and nasal microbiomes, possibly due to their interaction with the host and environment. Also, we identified individual-specific and commonly shared bacterial taxa, with individualized taxa showing greater stability. Interestingly, microbiome dynamics correlated across body sites, suggesting systemic coordination influenced by host-microbial-environment interactions. Notably, insulin-resistant individuals showed altered microbial stability and associations between microbiome, molecular markers, and clinical features, suggesting their disrupted interaction in metabolic disease. Our study offers comprehensive views of multi-site microbial dynamics and their relationship with host health and disease. Study HighlightsO_LIThe stability of the human microbiome varies among individuals and body sites. C_LIO_LIHighly individualized microbial genera are more stable over time. C_LIO_LIAt each of the four body sites, systematic interactions between the environment, the host and bacteria can be detected. C_LIO_LIIndividuals with insulin resistance have lower microbiome stability, a more diversified skin microbiome, and significantly altered host-microbiome interactions. C_LI

microbiology↗

Long-read sequencing of SARS-CoV-2 reveals novel transcripts and a diverse complex transcriptome landscape.

Severe Acute Respiratory Syndrome Coronavirus 2, SARS-CoV-2 (COVID-19), is a positive single-stranded RNA virus with a 30 kb genome that is responsible for the current pandemic. To date, the genomes of global COVID-19 variants have been primarily characterized via short-read sequencing methods. Here, we devised a long-read RNA (IsoSeq) sequencing approach to characterize the COVID-19 transcript landscape and expression of its [~]27 coding regions. Our analysis identified novel COVID-19 transcripts including a) a short [~]65-70 nt 5-UTR fused to various downstream ORFs encoding accessory proteins such as the envelope, ORF 8, and ORF 9 (nucleocapsid) proteins, that are relatively highly expressed, b) novel SNVs that are differentially expressed, whereby a subset are suggestive of partial RNA editing events, and c) SNVs at functional sites, whereby at least one is associated with a differentially expressed spike protein isoform. These previously uncharacterized COVID-19 isoforms, expressed genes, and gene variants were corroborated using ddPCR. Understanding this transcriptional complexity may help provide insight into the biology and pathogenicity of SARS-CoV-2 compared to other coronaviruses.

genetics↗