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Quackenbush, J.

Publications and source records attributed to Quackenbush, J..

At least 19 recordsLinked to original sources

FERRET: Framework to Evaluate Robustness in Regulatory Networks Using Heterogeneous Cell Types

Techniques for evaluating gene regulatory network (GRN) inference methods typically focus on recovering small ground-truth networks or on benchmarking against simulated data. However, both approaches have important limitations and fail to capture the biological variability present in real datasets. FERRET is a framework for benchmarking single-cell GRN inference methods based on a simple biological assumption: independent estimates of the regulatory network from the same cellular state should resemble one another more closely than estimates from distinct cellular states. Rather than relying on incomplete or simulated ground truth, FERRET quantifies network robustness using two complementary metrics: Robustness Area Under the Curve (RAUC), an AUC-like measure of within-cell-type network similarity relative to between-cell-type similarity, and Monotonicity, which assesses the consistency of network similarity across edge-weight cutoffs. FERRET also supports biological validation through pathway enrichment analysis. We validate FERRET using experimentally derived ChIP-seq networks from B lymphocytes and fibroblasts as positive controls and randomly generated networks as negative controls, showing that biologically related networks receive high robustness scores whereas randomly generated networks receive scores consistent with chance. Finally, we apply FERRET to multiple GRN inference methods on real single-cell RNA-sequencing datasets to identify methods that produce the most robust, biologically informative regulatory networks. GRAPHICAL ABSTRACT O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=112 SRC="FIGDIR/small/739795v1_ufig1.gif" ALT="Figure 1"> View larger version (43K): org.highwire.dtl.DTLVardef@da7e4eorg.highwire.dtl.DTLVardef@9a5425org.highwire.dtl.DTLVardef@a6e60org.highwire.dtl.DTLVardef@d466cd_HPS_FORMAT_FIGEXP M_FIG C_FIG

bioinformatics↗

Large-scale, interpretable gene regulatory network inference through biologically informed matrix factorization

Gene regulatory networks (GRNs) provide a mechanistic framework for understanding how transcription factors coordinate gene expression to establish cellular identity and phenotype. Methods that integrate gene expression with motif-derived regulatory priors and other sources of biological information have substantially advanced gene regulatory network inference by reconstructing condition-specific regulatory architecture. These approaches estimate the evidence supporting regulatory interactions and have proven remarkably successful in a wide range of biological applications. A complementary view of regulatory networks, however, seeks to estimate the effect of those interactions on gene expression itself, providing a framework in which regulatory edges can be interpreted as activating or inhibitory influences on transcription. We developed Giraffe, a biologically informed matrix factorization framework that jointly estimates transcription factor activities and gene regulatory networks by integrating gene expression, motif-based regulatory priors, and transcription factor protein-protein interactions. Giraffe estimates signed partial regulatory effects whose magnitude and sign can be interpreted as the strength and direction of transcriptional regulation. Building directly on the biological framework established by methods such as PANDA, Giraffe provides a complementary representation of gene regulatory networks that emphasizes mechanistic interpretation while remaining scalable, flexible, and computationally efficient. Across synthetic benchmarks, six human tissues, yeast transcription factor perturbation experiments, and liver hepatocellular carcinoma, Giraffe accurately reconstructs regulatory interactions while distinguishing activating from inhibitory regulation with high accuracy. The inferred networks recover known features of tissue-specific regulation, correctly classify regulatory effects in transcription factor perturbation experiments, and identify biologically coherent changes in regulatory programs associated with liver cancer. Together, these results demonstrate that estimating the direction of transcriptional regulation provides a complementary perspective on gene regulatory networks that facilitates biological interpretation and hypothesis generation.

systems biology↗

LOESS and DE-SWAN can induce artifactual "waves" of molecular aging

A growing body of literature has investigated the relationship between age and biomolecular changes, leading to conclusions that aging occurs in discrete molecular "waves." Data summary tools such as LOESS and sliding window analyses like DE-SWAN are common approaches that have gained acceptance in recent years. We demonstrate via simple simulations that these tools can identify non-linear patterns of aging where they do not exist. Specifically, we show that (i) clustering of molecular trajectories using LOESS can lead to artifactual characteristic patterns of molecular aging, (ii) "waves" of aging identified using the combination of LOESS and DE-SWAN in real data are not robust to changes in the underlying age distribution and are not supported by valid permutation testing, and (iii) DE-SWAN alone can generate pronounced "waves" of nonlinear molecular aging in linear data due to differences in statistical power along the age continuum. Our results specifically challenge the statistical support for discrete aging crests inferred in the literature, but do not rule out nonlinear molecular aging or age-associated transitions that may be detectable using other cohorts and statistical models.

bioinformatics↗

PARROT: Phase-Altering Regulatory Rewiring Over Time

MotivationGene regulatory networks undergo dynamic restructuring during development and disease. Identifying when and how these networks change is crucial for understanding developmental and disease transitions, yet existing change-point detection methods often ignore network structure or lack interpretable community assignments. ResultsWe present PARROT (Phase-Altering Regulatory Rewiring Over Time), a framework for detecting change-points in dynamic networks using Stochastic Block Models. PARROT jointly estimates change-point locations and community structure across four network classes: unipartite and bipartite with either Gaussian or Bernoulli edge models. Simulations demonstrate improved performance and community recovery compared to other methods. Applications to human cardiac differentiation and mouse lung development data successfully recovered known phase boundaries. PARROT identifies both which genes are reassigned across modules and how the connections change between states. AvailabilityPARROT is available as an R package at https://github.com/cchen22/PARROT. Contactchenchen9945@gmail.com Supplementary informationSupplementary data are available at Bioinformatics online.

bioinformatics↗

Sex differences in gene regulation and its impact on cancer incidence

Sex differences in the incidence rates of many cancer types are well-documented. While differences in lifestyle, environmental exposures, and hormone levels can influence disease risk and incidence, there is limited understanding of how cancer driver genes are differentially regulated between males and females in normal tissues, and how these differences may contribute to the observed sex differences in cancer epidemiology. We studied 8,279 gene regulatory networks across 29 non-cancerous tissues in the GTEx dataset, referred here as normal tissues. Using network centrality measures, we compared the networks between males and females, focusing on interactions between 644 transcription factors and 476 cancer genes (COSMIC Cancer Gene Census). Cancer genes were differentially targeted by transcription factors in males and females across normal tissues. We found an overrepresentation of sex-biased cancer genes on the X chromosome, particularly among genes escaping X chromosome inactivation, with higher regulatory targeting of tumor suppressor genes in females compared to males. Key signaling pathways, including WNT, NOTCH, and p53, showed differential transcriptional targeting by sex. We observed higher targeting of cancer-related pathways in females for tissues that have higher tumor incidence in females (breast, lung, and thyroid) and higher targeting in males for tissues with increased tumor incidence in males (stomach, colon, and liver). Sex-biased transcription factors that were consistently observed across multiple tissues are enriched for sex hormone response elements in their promoters. Our findings showed that normal tissues have sex-biased regulation of genes implicated in tumorigenesis, helping to explain the molecular basis of sex differences observed in cancer incidence rates and in identifying targets for cancer prevention in a sex-aware manner.

systems biology↗

Sex differences in thyroid aging and their implications in thyroid disorders: insights from gene regulatory networks

Thyroid disorders are more prevalent in females than males, with sex differences in disease risk varying by age, e.g. although risk of anaplastic thyroid carcinoma (ATC) increases with age for both sexes, females are diagnosed at younger ages than males. In contrast, Hashimotos thyroiditis (HT) is more common in ages 30-50, with females having higher risk. These patterns suggest that in thyroid, gene regulatory processes evolve with age in a sex-specific manner. To characterize these sex differences in thyroid aging, we estimated and analyzed individual-specific gene regulatory networks using BONOBO and PANDA algorithms. We found that regulatory patterns of pathways involved in cell proliferation, immune response, and metabolic processes vary nonlinearly with age, with sex-specific differences in direction and rate. Females show two inflection points around ages 40 and 60, when regulatory patterns show significant change for most pathways, consistent with changes in targeting by estrogen and androgen receptors. Investigating gene regulatory patterns in HT and ATC, we observed that disease-relevant immune and metabolic pathways changed with age in the same direction as they change in ATC. In contrast, in HT, disease-related regulatory patterns are in the opposite direction of aging. In age groups where HT is most diagnosed, regulatory patterns in females more closely resembled disease states than males, highlighting sex-biased regulations role in elevated disease risk in females. Our findings demonstrate immune response and metabolic processes are regulated in age- and sex-specific manner, potentially driving variation in disease risk, emphasizing the need for tailored screening and prevention strategies. O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=113 SRC="FIGDIR/small/684890v3_ufig1.gif" ALT="Figure 1"> View larger version (39K): org.highwire.dtl.DTLVardef@cd93aeorg.highwire.dtl.DTLVardef@9a913aorg.highwire.dtl.DTLVardef@1b4a862org.highwire.dtl.DTLVardef@19adca8_HPS_FORMAT_FIGEXP M_FIG C_FIG

systems biology↗

SEAHORSE: A Serendipity Engine Assaying Heterogeneous Omics-Related Sampling Experiments

Large public molecular atlases such as the Genotype-Tissue Expression (GTEx) project and The Cancer Genome Atlas (TCGA) invite systematic discovery, yet most analyses remain hypothesis-driven and interrogate a tiny fraction of possible relationships among phenotypic, clinical, and molecular variables. We developed SEAHORSE (Serendipity Engine Assaying Heterogeneous Omics-Related Sampling Experiments), a discovery engine and accompanying R package that exhaustively precomputes all pairwise associations across heterogeneous data types and presents them as a searchable association landscape. Using GTEx (948 donors, 43 tissues, 154 phenotypes), SEAHORSE generated 341,008 phenotype-phenotype associations, 125,246,938 phenotype-gene associations, and 10,269,910,410 gene-gene correlations. In parallel analyses spanning 33 tumor types in TCGA, SEAHORSE generated 625,042 phenotype-phenotype associations, 183,080,369 phenotype-gene associations, and 12,096,948,950 gene-gene correlations. Across GTEx, height was repeatedly associated with enrichment of transcriptional programs, most strikingly the Kyoto Encyclopedia of Genes and Genomes (KEGG) term "Pathways in Cancer," significant in 17 tissues, offering a molecular entry point into long-reported links between stature and cancer risk. Height was also associated with immune, cardiovascular, and neurologic programs. In TCGA, age was consistently associated with WNT signaling, translation, cell differentiation, and cell cycle programs across tumors. These findings illustrate a new paradigm: large cohorts should be treated not merely as repositories for testing preconceived hypotheses but as association landscapes that can generate unexpected biological hypotheses.

bioinformatics↗

BLOBFISH: Bipartite Limited Subnetworks from Multiple Observations using Breadth-First Search with Constrained Hops

SummaryIn analyzing gene regulatory network models, a common question is how members of a particular set of genes are connected. For example, one might want to explore network relationship between a set of differentially expressed genes, a gene set previously reported in the literature, or elements of one or more pathways. BLOBFISH uses a breadth-first search algorithm adapted to bipartite graphs to identify a compact subnetwork connecting the members of a pre-specified set of genes, providing a regulatory context that can shed light on specific mechanisms involved in a phenotype and its development. We demonstrate the use of BLOBFISH to extract gene regulatory subnetworks reflecting tissue specificity using publicly available data from the Genotype Tissue Expression (GTEx) project.

bioinformatics↗

Identifying Sex Differences in Lung Adenocarcinoma Using Multi-Omics Integrative Protein Signaling Networks

Lung adenocarcinoma (LUAD) exhibits differences between the sexes in incidence, prognosis, and therapy, suggesting underexplored molecular mechanisms. We conducted an integrative multi-omics analysis using the Clinical Proteomic Tumor Analysis Consortium (CPTAC) and The Cancer Genome Atlas (TCGA) datasets to contrast transcriptomes and proteomes between sexes. We used TIGER to analyze TCGA-LUAD expression data and found sex-biased activity of transcription factors (TFs); we used PTM-SEA with CPTAC-LUAD proteomics data and found sex-biased kinase activity. We combined these to construct a kinase-TF signaling network and discovered druggable pathways linked to cancer-related processes. We also found significant sex biases in clinically relevant TFs and kinases, including NR3C1, AR, and AURKA. Using the PRISM drug screening database, we identified potential sex-specific drugs, such as glucocorticoid receptor agonists and aurora kinase inhibitors. Our findings emphasize the importance of considering sex and using multi-omics network methods to discover personalized cancer therapies.

cancer biology↗

Reproducible processing of TCGA regulatory networks

BackgroundTechnological advances in sequencing and computation have allowed deep exploration of the molecular basis of diseases. Biological networks have proven to be a useful framework for interrogating omics data and modeling regulatory gene and protein interactions. Large collaborative projects, such as The Cancer Genome Atlas (TCGA), have provided a rich resource for building and validating new computational methods resulting in a plethora of open-source software for downloading, pre-processing, and analyzing those data. However, for an end-to-end analysis of regulatory networks a coherent and reusable workflow is essential to integrate all relevant packages into a robust pipeline. FindingsWe developed tcga-data-nf, a Nextflow workflow that allows users to reproducibly infer regulatory networks from the thousands of samples in TCGA using a single command. The workflow can be divided into three main steps: multi-omics data, such as RNA-seq and methylation, are downloaded, preprocessed, and lastly used to infer regulatory network models with the netZoo software tools. The workflow is powered by the NetworkDataCompanion R package, a standalone collection of functions for managing, mapping, and filtering TCGA data. Here we show how the pipeline can be used to study the differences between colon cancer subtypes that could be explained by epigenetic mechanisms. Lastly, we provide pre-generated networks for the 10 most common cancer types that can be readily accessed. Conclusionstcga-data-nf is a complete yet flexible and extensible framework that enables the reproducible inference and analysis of cancer regulatory networks, bridging a gap in the current universe of software tools.

bioinformatics↗

Selective loss of Y chromosomes in lung adenocarcinoma modulates the tumor immune environment through cancer/testis antigens

There is increasing recognition that the allosomes, X and Y, play an important role in health and disease beyond the determination of biological sex. A loss of the Y chromosome (LOY) occurs in most solid tumors in males and is often associated with worse survival, suggesting that LOY may give tumor cells a growth or survival advantage. We here use an expression-based continuous measure of LOY that allows us to investigate LOY in lung adenocarcinoma (LUAD) using both bulk and single-cell expression data. We find evidence suggesting that LOY affects the tumor immune environment by altering cancer/testis antigen expression and consequently facilitating tumor immune evasion, also reflected in inferred gene regulatory networks. In immunotherapy data, we further show that LOY and changes in expression of particular cancer/testis antigens are associated with response to pembrolizumab treatment and outcome. This computational study provides new insights into the mechanisms behind LOY in LUAD and a powerful biomarker for predicting immunotherapy response in LUAD tumors in males.

cancer biology↗

Aging-associated Alterations in the Gene Regulatory Network Landscape Associate with Risk, Prognosis and Response to Therapy in Lung Adenocarcinoma

Aging is the primary risk factor for many individual cancer types, including lung adenocarcinoma (LUAD). To understand how aging-related alterations in the regulation of key cellular processes might affect LUAD risk and survival outcomes, we built individual (person)-specific gene regulatory networks integrating gene expression, transcription factor protein-protein interaction, and sequence motif data, using PANDA/LIONESS algorithms, for both non-cancerous lung tissue samples from the Genotype Tissue Expression (GTEx) project and LUAD samples from The Cancer Genome Atlas (TCGA). In GTEx, we found that pathways involved in cell proliferation and immune response are increasingly targeted by regulatory transcription factors with age; these aging-associated alterations are accelerated by tobacco smoking and resemble oncogenic shifts in the regulatory landscape observed in LUAD and suggests that dysregulation of aging pathways might be associated with an increased risk of LUAD. Comparing normal adjacent samples from individuals with LUAD with healthy lung tissue samples from those without LUAD, we found that aging-associated genes show greater aging-biased targeting patterns in younger individuals with LUAD compared to their healthy counterparts of similar age, a pattern suggestive of age acceleration. This implies that an accelerated aging process may be responsible for tumor incidence in younger individuals. Using drug repurposing tool CLUEreg, we found small molecule drugs with potential geroprotective effects that may alter the accelerating aging profiles we found. We also observed that, in contrast to chronological age, a network-informed aging signature was associated with survival and response to chemotherapy in LUAD. Graphical abstract O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=113 SRC="FIGDIR/small/601689v1_ufig1.gif" ALT="Figure 1"> View larger version (32K): org.highwire.dtl.DTLVardef@1a8c735org.highwire.dtl.DTLVardef@1ae8833org.highwire.dtl.DTLVardef@16fd65dorg.highwire.dtl.DTLVardef@16287e5_HPS_FORMAT_FIGEXP M_FIG C_FIG

cancer biology↗

node2vec2rank: Large Scale and Stable Graph Differential Analysis via Multi-Layer Node Embeddings and Ranking

1Advances in computational biology now enable the inference of increasingly accurate, genome-wide molecular interaction networks from multi-omic data collected across large cohorts. Comparing such networks across distinct biological states can identify biologically informative and potentially actionable higher-order interactions that differentiate these states. However, developing methods for effective graph differential analysis remains challenging as it requires capturing subtle structural changes within the context of complex, high-dimensional networks shaped by heterogeneous biological processes. We introduce node2vec2rank (n2v2r), a multi-layer spectral embedding algorithm that, in contrast to conventional feature-based approaches, compares graphs by inferring node representations that summarize network structure in a data-driven manner. Node2vec2rank is computationally efficient, stable, and provably recovers the correct ranking of differences between weighted graphs. We used n2v2r to compare networks from breast cancer subtypes, to analyze networks capturing single-cell dynamics, and to investigate sex differences in lung adenocarcinoma. The results of these analyses show that n2v2r is a versatile and powerful tool that can uncover biologically relevant insights from complex biological networks, distinguishing between states of health and disease.

bioinformatics↗

Complex Traits Heritability is Highly Clustered in the eQTL Bipartite Network

Complex traits are determined by many loci--mostly regulatory elements--that, through combinatorial interactions, can affect multiple traits. Such high levels of epistasis and pleiotropy have been proposed in the omnigenic model and may explain why such a large part of complex trait heritability is usually missed by genome-wide association studies while raising questions about the possibility for such traits to evolve in response to environmental constraints. To explore the molecular bases of complex traits and understand how they can adapt, we systematically analyzed the distribution of SNP heritability for ten traits across 29 tissue-specific Expression Quantitative Trait Locus (eQTL) networks. We find that heritability is clustered in a small number of tissue-specific, functionally relevant SNP-gene modules and that the greatest heritability occurs in local "hubs" that are both the cornerstone of the networks modules and tissue-specific regulatory elements. The network structure could thus both amplify the genotype-phenotype connection and buffer the deleterious effect of the genetic variations on other traits. We confirm that this structure has allowed complex traits to evolve in response to environmental constraints, with the local "hubs" being the preferential targets of past and ongoing directional selection. Together, these results provide a conceptual framework for understanding complex trait architecture and evolution.

systems biology↗

Polygenic basis of field evolved Bt Cry resistance in the corn earworm, Helicoverpa zea

Strong and shifting selective pressures of the anthropocene are rapidly shaping phenomes and genomes of organisms worldwide. One major selective force on insect genomes is crops expressing pesticidal proteins from Bacillus thuringiensis (Bt). Here we characterize a rapid response to selection by Bt crops in a major crop pest, Helicoverpa zea. We reveal the polygenic architecture of Bt resistance evolution in H. zea and identify multiple genomic regions underlying this trait. In the genomic region of largest effect, we identified a gene cluster amplification, where resistant individuals showed variation in copy number for multiple genes. Signals of this amplification increased over time, consistent with the history of field-evolved Bt resistance evolution. Modern wild populations from disparate geographical regions are positive for this variant at high, but not fixed, allele frequencies. We also detected selection against single copy variants at this locus in wild H. zea collected from Bt expressing plants, further supporting its role in resistance. Seven trypsin genes were present in this genomic region and all appeared to be significantly upregulated in Bt resistant H. zea. Biochemically inhibiting trypsin activity decreased H. zeas tolerance to Bt. These findings characterize rapid genome evolution in a major crop pest following anthropogenic selection and highlight the role that gene copy number variants can have in rapid evolutionary responses.

evolutionary biology↗

Higher-order correction of persistent batch effects in correlation networks

Systems biology methods often rely on correlations in gene expression profiles to infer co-expression networks, commonly used as input for gene regulatory network inference or to identify functional modules of co-expressed or co-regulated genes. While systematic biases, including batch effects, are known to induce spurious associations and confound differential gene expression analyses (DE), the impact of batch effects on gene co-expression has not been fully explored. Methods have been developed to adjust expression values, ensuring conditional independence of mean and variance from batch or other covariates for each gene. These adjustments have been shown to improve the fidelity of DE analysis. However, these methods do not address the potential for spurious differential co-expression (DC) between groups. Consequently, uncorrected, artifactual DC can skew the correlation structure, leading network inference methods that use gene co-expression to identify false, nonbiological associations, even when the input data is corrected using standard batch correction. In this work, we demonstrate the persistence of confounders in covariance after standard batch correction using synthetic and real-world gene expression data examples. Subsequently, we introduce Co-expression Batch Reduction Adjustment (COBRA), a method for computing a batch-corrected gene co-expression matrix based on estimating a conditional covariance matrix. COBRA estimates a reduced set of parameters expressing the co-expression matrix as a function of the sample covariates, allowing control for continuous and categorical covariates. COBRA is computationally efficient, leveraging the inherently modular structure of genomic data to estimate accurate gene regulatory associations and facilitate functional analysis for high-dimensional genomic data.

bioinformatics↗

Bayesian Optimized sample-specific Networks Obtained ByOmics data (BONOBO)

Gene regulatory networks (GRNs) are effective tools for inferring complex interactions between molecules that regulate biological processes and hence can provide insights into drivers of biological systems. Inferring co-expression networks is a critical element of GRN inference as the correlation between expression patterns may indicate that genes are coregulated by common factors. However, methods that estimate co-expression networks generally derive an aggregate network representing the mean regulatory properties of the population and so fail to fully capture population heterogeneity. To address these concerns, we introduce BONOBO (Bayesian Optimized Networks Obtained By assimilating Omics data), a scalable Bayesian model for deriving individual sample-specific co-expression networks by recognizing variations in molecular interactions across individuals. For every sample, BONOBO assumes a Gaussian distribution on the log-transformed centered gene expression and a conjugate prior distribution on the sample-specific co-expression matrix constructed from all other samples in the data. Combining the sample-specific gene expression with the prior distribution, BONOBO yields a closed-form solution for the posterior distribution of the sample-specific co-expression matrices, thus making the method extremely scalable. We demonstrate the utility of BONOBO in several contexts, including analyzing gene regulation in yeast transcription factor knockout studies, prognostic significance of miRNA-mRNA interaction in human breast cancer subtypes, and sex differences in gene regulation within human thyroid tissue. We find that BONOBO outperforms other sample-specific co-expression network inference methods and provides insight into individual differences in the drivers of biological processes. Graphical Abstract O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=191 SRC="FIGDIR/small/567119v1_ufig1.gif" ALT="Figure 1"> View larger version (38K): org.highwire.dtl.DTLVardef@f97de5org.highwire.dtl.DTLVardef@1b864a9org.highwire.dtl.DTLVardef@d8a384org.highwire.dtl.DTLVardef@d73091_HPS_FORMAT_FIGEXP M_FIG C_FIG

genomics↗

Gene regulatory Networks Reveal Sex Difference in Lung Adenocarcinoma

Lung adenocarcinoma (LUAD) has been observed to have significant sex differences in incidence, prognosis, and response to therapy. However, the molecular mechanisms responsible for these disparities have not been investigated extensively. Sample-specific gene regulatory network methods were used to analyze RNA sequencing data from non-cancerous human lung samples from The Genotype Tissue Expression Project (GTEx) and lung adenocarcinoma primary tumor samples from The Cancer Genome Atlas (TCGA); results were validated on independent data. We observe that genes associated with key biological pathways including cell proliferation, immune response and drug metabolism are differentially regulated between males and females in both healthy lung tissue, as well as in tumor, and that these regulatory differences are further perturbed by tobacco smoking. We also uncovered significant sex bias in transcription factor targeting patterns of clinically actionable oncogenes and tumor suppressor genes, including AKT2 and KRAS. Using differentially regulated genes between healthy and tumor samples in conjunction with a drug repurposing tool, we identified several small-molecule drugs that might have sex-biased efficacy as cancer therapeutics and further validated this observation using an independent cell line database. These findings underscore the importance of including sex as a biological variable and considering gene regulatory processes in developing strategies for disease prevention and management.

cancer biology↗