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Reese, J.

Publications and source records attributed to Reese, J..

10 recordsLinked to original sources

Scalable spatial DNA sequencing from archival tissue maps copy number subclones

Spatially resolved DNA sequencing holds promise due to its potential utility in understanding cancer intra-tumour heterogeneity and tumour evolution in relation to tissue architecture. However, it has so far been used to a limited extent due to technical challenges and high cost of existing methods. Hence we aimed to develop a high throughput spatial genomic assay to obtain copy number alteration (CNA) information at user-defined spatial resolution. We derived CNA profiles from ultra-low coverage whole genome sequencing at sub-millimetre resolution from archival samples using a novel method called Adaptive Resolution Multiscale Spatial DNA sequencing (ARMS DNAseq). We used it to profile CNAs from more than 766 regions (tiles) from 3 patients, covering a total area of over 300 mm2, with 1.2-2.6 million mapped reads per tile and tile sizes of 0.1-0.99mm2. Using ARMS DNAseq, we delineate tumour evolution in a spatial context, and identify more tumour subclones that were obscured or incompletely represented in bulk multi-region whole genome sequencing. Next, we show associations between tumour subclones and morphology, and prediction of subclone identity from deep learning-derived image representations. Finally, we demonstrate multi-omic integration by alignment with spatial transcriptomic data, showing subclone-specific immune cell co-occurrence as well as transcriptional programmes cutting across subclone boundaries. ARMS DNAseq converts low-throughput, region-by-region profiling into a scalable and adaptable workflow for direct spatial copy number profiling from archival tissue sections.

genomics↗

Performance of Information Theory Derived Semantic Similarity Algorithms for Differential Diagnosis and Clustering

Semantic similarity analysis with Human Phenotype Ontology (HPO) enables fuzzy, specificity weighted comparisons of clinical manifestations of individuals and diseases and can be used to support differential diagnostics or to stratify cohorts. Many methods have been proposed to calculate semantic similarity for various applications, including the Phenomizer, which calculates the average best match over all terms in the query and disease, and set-based methods ranging from the Jaccard Intersection to methods that leverage the conditional information content to calculate similarity. However, these methods have not been described under a single mathematical model or robustly compared using a comprehensive data set. Here, we describe several semantic similarity algorithms using derivations based on information theory, propose three of our own variations to these models, and compare the performance of each approach for differential diagnostic ranking and phenotypic clustering. We find that Phenomizer performs better when diseases are ranked by similarity alone, without generating p-values. Additionally, non-normalized algorithms that use conditional information perform similarly to Phenomizer for differential diagnosis. In contrast, normalized algorithms perform best when clustering cohorts. AvailabilityData is available through the Phenopacket-Store (https://github.com/monarch-initiative/phenopacket-store). Algorithms are implemented in the Python package SetSim (https://github.com/P2GX/setsim).

bioinformatics↗

KG-Microbe - Building Modular and Scalable Knowledge Graphs for Microbiome and Microbial Sciences

The integration of many disparate forms of data is essential for understanding the microbial world and its interaction with the environment and human health. Doing so is particularly challenging in the context of microbe-host and microbe-microbe interactions that contribute to health or environmental outcomes. There are often thousands of relevant microbial species, and millions of interactions among those microbes and with their environment or host. Some experimental observations only distinguish coarser taxonomic resolutions such as family or phylum-level. Integrated information (e.g., about host and microbial physiology, genetics, and metabolism) facilitates deeper understanding of complex interactions and helps interpret correlative results. The KG-Microbe construction framework is a novel approach to harmonizing bacterial and archaeal data in the form of a knowledge graph (KG). Starting from a core KG with organismal traits, environments and growth preferences, the framework generates a hierarchy of related KGs targeting specific conceptual use cases, including the human host-associated microbiome in the context of disease. KG-Microbe is a standardized and interoperable framework that integrates microbial organismal and genomic traits, represented ontologically, for biomedical, environmental, and other applications. The framework supports customizable taxa subsets representing microbial lineages or communities of interest. Evaluations of the KG-Microbe knowledge graphs through a series of competency questions demonstrate the accuracy and effectiveness of the data harmonization, and the utility of the resulting KGs in inflammatory bowel and Parkinsons diseases. Finally, the predictive and environmental capabilities of the KGs are demonstrated by explaining growth preferences through training a model using graph features. KG-Microbe is a flexible, modular enabling technology for humans and machine learning methods to uncover mechanistic explanations of microbial associations.

bioinformatics↗

Intrinsic-Dimension analysis for guiding dimensionality reduction and data fusion in multi-omics data processing

The advent of high-throughput sequencing technologies has revolutionized the field of multi-omics patient data analysis. While these techniques offer a wealth of information, they often generate datasets with dimensions far surpassing the number of available cases. This discrepancy in size gives rise to the challenging "small-sample-size" problem, significantly compromising the reliability of any subsequent estimate, whether supervised or unsupervised. This calls for effective dimensionality reduction techniques to transform high-dimensional datasets into lower-dimensional spaces, making the data manageable and facilitating subsequent analyses. Unfortunately, the definition of a proper di-mensionality reduction pipeline is not an easy task; besides the problem of identifying the best dimensionality reduction method, the definition of the dimension of the lower-dimensional space into which each dataset should be transformed is a crucial issue that influences all the subsequent analyses and should therefore be carefully considered. Further, the availability of multi-modal data calls for proper data-fusion techniques to produce an integrated patient-view into which redundant information is removed while salient and complementary information across views is leveraged to improve the performance and reliability of both unsupervised and supervised learning techniques. This paper proposes leveraging the intrinsic dimensionality of each view in a multi-modal dataset to define the dimensionality of the lower-dimensional space where the view is transformed by dimensionality reduction algorithms. Further, it presents a thorough experimental study that compares the traditional application of a unique-step of dimensionality reduction with a two-step approach, involving a prior feature selection followed by feature extraction. Through this comparative evaluation, we scrutinize the performance of widely used dimensionality reduction algorithms. Importantly, we also investigate their impact on unsupervised data-fusion techniques, which are pivotal in biomedical research. Our findings shed light on the most effective strategies for handling high-dimensional multi-omics patient data, offering valuable insights for future studies in this domain. Graphical Abstract O_FIG O_LINKSMALLFIG WIDTH=159 HEIGHT=200 SRC="FIGDIR/small/576822v1_ufig1.gif" ALT="Figure 1"> View larger version (56K): org.highwire.dtl.DTLVardef@c39539org.highwire.dtl.DTLVardef@79f681org.highwire.dtl.DTLVardef@1269fcforg.highwire.dtl.DTLVardef@c5e31d_HPS_FORMAT_FIGEXP M_FIG C_FIG HighlightsO_LIWe introduce a flexible pipeline to guide in a principled way feature selection and feature extraction methods to reduce the high dimensions and to contrast the curse of dimensionality that affects multi-omics data. C_LIO_LIWe harness the power of cutting-edge Intrinsic Dimensionality (id) estimation through block-analysis, providing an unbiased estimation of the individual ids for each view within a multi-modal dataset. C_LIO_LIWe use an exhaustive set of diverse multi-omics cancer datasets from the well-known TCGA dataset to show that the automatic analysis of the distribution of the block-ids characterizing each omics-view leverages dimensionality reduction, by (1) evidencing feature noise and redundancy, and (2) providing an unbiased estimate of the id for each view, to be used for setting the dimension of the reduced space. This avoids empirical or heuristic choices and allows tailoring the reduction to each data-view. C_LIO_LIThe crucial information gained by block-analysis allowed proposing a two-step dimensionality-reduction approach combining feature selection and feature extraction. Our comparative evaluation shows the effectiveness of the proposed technique and its synergy with state-of-the-art data-fusion techniques applied in a multi-omics context. C_LIO_LIWe show that the proposed reduction pipeline leverages traditional dimensionality reduction and state-of-the-art data-fusion algorithms. Indeed, it obtains effective performance when predicting overall survival events with simple random forest classifiers, often preferred in the biomedical field due to their robustness, efficiency, and interpretable nature. C_LI

bioinformatics↗

Effects of pasteurization on osteopontin levels in human breastmilk and pasteurized breastmilk products

BackgroundOsteopontin (OPN) is an important breastmilk protein involved in infant intestinal, immunological, and brain development. However, little is known about how common milk pasteurization and storage techniques affect this important bioactive protein. MethodsHuman milk osteopontin concentration was measured in single-donor fresh or frozen breastmilk, pooled Holder-pasteurized donor breastmilk, and a shelf-stable (retort pasteurized) breastmilk product by ELISA. Breastmilk samples were pasteurized and/or frozen before measuring osteopontin concentrations. ResultsHolder pasteurization of breastmilk resulted in an [~]50% decrease in osteopontin levels within single-donor samples, whereas pooled donor breastmilk had comparable osteopontin levels to non-pasteurized single-donor samples. Breastmilk from mothers of preterm infants trended toward higher osteopontin concentration than mothers of term infants; however, samples from preterm mothers experienced greater osteopontin degradation upon pasteurization. Finally, freezing breastmilk prior to Holder pasteurization resulted in less osteopontin degradation than Holder pasteurization prior to freezing. ConclusionCommonly used breastmilk pasteurization and storage techniques, including freezing, Holder and retort pasteurization, decrease the levels of the bioactive protein osteopontin in human breastmilk. ImpactO_LIPasteurization of human breastmilk significantly decreases the levels of the bioactive protein osteopontin C_LIO_LIUse of both pasteurization and freezing techniques for breastmilk preservation results in greater loss of osteopontin C_LIO_LIThis study presents for the first time an analysis of osteopontin levels in single-donor pasteurized milk samples C_LI

physiology↗

Node-degree aware edge sampling mitigates inflated classification performance in biomedical graph representation learning

Graph representation learning is a family of related approaches that learn low-dimensional vector representations of nodes and other graph elements called embeddings. Embeddings approximate characteristics of the graph and can be used for a variety of machine-learning tasks such as novel edge prediction. For many biomedical applications, partial knowledge exists about positive edges that represent relationships between pairs of entities, but little to no knowledge is available about negative edges that represent the explicit lack of a relationship between two nodes. For this reason, classification procedures are forced to assume that the vast majority of unlabeled edges are negative. Existing approaches to sampling negative edges for training and evaluating classifiers do so by uniformly sampling pairs of nodes. We show here that this sampling strategy typically leads to sets of positive and negative edges with imbalanced edge degree distributions. Using representative homogeneous and heterogeneous biomedical knowledge graphs, we show that this strategy artificially inflates measured classification performance. We present a degree-aware node sampling approach for sampling negative edge examples that mitigates this effect and is simple to implement.

bioinformatics↗

An algorithmic framework for isoform-specific functional analysis

Gene Ontology (GO) overrepresentation analysis characterizes the biological mechanisms common to sets of differentially expressed genes identified by high-throughput experiments. To date, GO overrepresentation analysis has mainly been used to evaluate differentially expressed genes, but short- and long-read RNA-seq technologies now allow increasingly accurate identification of differential alternative splicing. The function of most splice isoforms remain unknown, but if acccurate predictions could be made, overrepresentation analysis could be applied to differentially spliced isoforms to assess the functional implications of alternative splicing in RNA-seq experiments. We present isopret (Isoform Interpretation), a new paradigm for isoform function prediction based on the expectation-maximization framework. isopret leverages the relationships between sequence and functional isoform similarity to infer isoform specific functions in a highly accurate fashion. This enabled us to adapt GO overrepresentation analysis, which to date has been limited to differential gene expression, to be extended to assess overrepresentation of GO annotations in differentially spliced isoforms. An analysis of 100 RNA-seq studies including investigations of development, cancer, and common disease demonstrated that expression and splicing regulate different sets of biological functions. We make isopret predictions freely available in a desktop application that can be used to analyze differential expression and splicing in any bulk RNA-seq dataset.

bioinformatics↗

SvAnna: efficient and accurate pathogenicity prediction for coding and regulatory structural variants in long-read genome sequencing

Structural variants (SVs) are implicated in the etiology of Mendelian diseases but have been systematically underascertained owing to limitations of existing technology. Recent technological advances such as long-read sequencing (LRS) enable more comprehensive detection of SVs, but approaches for clinical prioritization of candidate SVs are needed. Existing computational approaches do not specifically target LRS data, thereby missing a substantial proportion of candidate SVs, and do not provide a unified computational model for assessing all types of SVs. Structural Variant Annotation and Analysis (SvAnna) assesses all classes of SV and their intersection with transcripts and regulatory sequences in the context of topologically associating domains, relating predicted effects on gene function with clinical phenotype data. We show with a collection of 182 published case reports with pathogenic SVs that SvAnna places over 90% of pathogenic SVs in the top ten ranks. The interpretable prioritizations provided by SvAnna will facilitate the widespread adoption of LRS in diagnostic genomics.

bioinformatics↗

Supervised learning with word embeddings derived from PubMed captures latent knowledge about protein kinases and cancer

Inhibiting protein kinases (PKs) that cause cancers has been an important topic in cancer therapy for years. So far, almost 8% of more than 530 PKs have been targeted by FDA-approved medications and around 150 protein kinase inhibitors (PKIs) have been tested in clinical trials. We present an approach based on natural language processing and machine learning to the relations between PKs and cancers, predicting PKs whose inhibition would be efficacious to treat a certain cancer. Our approach represents PKs and cancers as semantically meaningful 100-dimensional vectors based on co-occurrence patterns in PubMed abstracts. We use information about phase I-IV trials in ClinicalTrials.gov to construct a training set for random forest classification. In historical data, associations between PKs and specific cancers could be predicted years in advance with good accuracy. Our model may be a tool to predict the relevance of inhibiting PKs with specific cancers.

bioinformatics↗

Identification of mundulone and mundulone acetate as natural products with tocolytic efficacy in mono- and combination-therapy with current tocolytics

Currently, there are a lack of FDA-approved tocolytics for the management of preterm labor. We previously observed that the isoflavones mundulone and mundulone acetate (MA) inhibit intracellular Ca2+-regulated myometrial contractility. Here, we further probed the potential of these natural products to be small molecule leads for discovery of novel tocolytics by: (1) examining uterine-selectivity by comparing concentration-response between human primary myometrial cells and a major off-target site, aortic vascular smooth muscle cells (VSMCs), (2) identifying synergistic combinations with current clinical tocolytics to increase efficacy or and reduce off-target side effects, (3) determining cytotoxic effects and (4) investigating the efficacy, potency and tissue-selectivity between myometrial contractility and constriction of fetal ductus arteriosus (DA), a major off-target of current tocolytics. Mundulone displayed significantly greater efficacy (Emax = 80.5% vs. 44.5%, p=0.0005) and potency (IC50 = 27 M and 14 M, p=0.007) compared to MA in the inhibition of intracellular-Ca2+ from myometrial cells. MA showed greater uterine-selectivity, compared to mundulone, based on greater differences in the IC50 (4.3 vs. 2.3 fold) and Emax (70% vs. 0%) between myometrial cells compared to aorta VSMCs. Moreover, MA demonstrated a favorable in vitro therapeutic index of 8.8, compared to TI = 0.8 of mundulone, due to its significantly (p<0.0005) smaller effect on the viability of myometrial (hTERT-HM), liver (HepG2) and kidney (RPTEC) cells. However, mundulone exhibited synergism with two current tocolytics (atosiban and nifedipine), while MA only displayed synergistic efficacy with only nifedipine. Of these synergistic combinations, only mundulone + atosiban demonstrated a favorable TI = 10 compared to TI=0.8 for mundulone alone. While only mundulone showed concentration-dependent inhibition of ex vivo mouse myometrial contractions, neither mundulone or MA affected mouse fetal DA vasoreactivity. The combination of mundulone and atosiban yielded greater tocolytic efficacy and potency on term pregnant mouse and human myometrial tissue compared to single-drugs. Collectively, these data highlight the difference in uterine-selectivity of Ca2+-mobilization, effects on cell viability and tocolytic efficacy between mundulone and MA. These natural products could benefit from medicinal chemistry efforts to study the structural activity relationship for further development into a promising single- and/or combination-tocolytic therapy for management of preterm labor. Chemical compounds studied in this articleatosiban (Pubchem CID: 5311010); indomethacin (Pubchem CID: 3715); mundulone (Pubchem CID: 4587968); mundulone acetate (Pubchem CID: 6857790); nifedipine (Pubchem CID: 4485); oxytocin acetate (Pubchem CID: 5771); U46619 (Pubchem CID: 5311493)

pharmacology and toxicology↗