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Ghazi, A. R.

Publications and source records attributed to Ghazi, A. R..

4 recordsLinked to original sources

scDiagnostics: systematic assessment of cell type annotation in single-cell transcriptomics data

Although cell type annotation has become an integral part of single-cell analysis workflows, the assessment of computational annotations remains challenging. Many annotation tools transfer labels from an annotated reference dataset to a new query dataset of interest, but blindly transferring labels from one dataset to another has its own set of challenges. Often enough there is no perfect alignment between datasets, especially when transferring annotations from a healthy reference atlas for the discovery of disease states. We present scDiagnostics, a new open-source software package that facilitates the detection of complex or ambiguous annotation cases that may otherwise go unnoticed, thus addressing a critical unmet need in current single-cell analysis workflows. scDiagnostics is equipped with novel diagnostic methods that are compatible with all major cell type annotation tools. We demonstrate that scDiagnostics reliably detects complex or conflicting annotations using both carefully designed simulated datasets and diverse real-world single-cell datasets. Our evaluation demonstrates that scDiagnostics reliably identifies misleading annotations that systematically distort downstream analysis and interpretation and that would otherwise remain undetected. The scDiagnostics R package is available from Bioconductor (https://bioconductor.org/packages/scDiagnostics).

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Quantifying Metagenomic Strain Associations fromMicrobiomes with Anpan

Genetic and genomic variation among microbial strains can dramatically influence their phenotypes and environmental impact, including on human health. However, inferential methods for quantifying these differences have been lacking. Strain-level metagenomic profiling data has several features that make traditional statistical methods challenging to use, including high dimensionality, extreme variation among samples, and complex phylogenetic relatedness. We present Anpan, a set of quantitative methods addressing three key challenges in microbiome strain epidemiology. First, adaptive filtering designed to interrogate microbial strain gene carriage is combined with linear models to identify strain-specific genetic elements associated with host health outcomes and other phenotypes. Second, phylogenetic generalized linear mixed models are used to characterize the association of sub-species lineages with such phenotypes. Finally, random effects models are used to identify pathways more likely to be retained or lost by outcome-associated strains. We validated our methods by simulation, showing that we achieve more accurate effect size estimation and a lower false positive rate compared to alternative methodologies. We then applied our methods to a dataset of 1,262 colorectal cancer patients, identifying functionally adaptive genes and strong phylogenetic effects associated with CRC status, sometimes complementing and sometimes extending known species-level microbiome CRC biomarkers. Anpans methods have been implemented as a publicly available R library to support microbial community strain and genetic epidemiology in a variety of contexts, environments, and phenotypes.

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High-sensitivity pattern discovery in large, paired multi-omic datasets

Modern biological screens yield enormous numbers of measurements, and identifying and interpreting statistically significant associations among features is essential. Here, we present a novel hierarchical framework, HAllA (Hierarchical All-against-All association testing), for structured association discovery between paired high-dimensional datasets. HAllA efficiently integrates hierarchical hypothesis testing with false discovery rate correction to reveal significant linear and non-linear block-wise relationships among continuous and/or categorical data. We optimized and evaluated HAllA using heterogeneous synthetic datasets of known association structure, where HAllA outperformed all-against-all and other block testing approaches across a range of common similarity measures. We then applied HAllA to a series of real-world multi-omics datasets, revealing new associations between gene expression and host immune activity, the microbiome and host transcriptome, metabolomic profiling, and human health phenotypes. An open-source implementation of HAllA is freely available at http://huttenhower.sph.harvard.edu/halla along with documentation, demo datasets, and a user group. Author SummaryModern scientific datasets increasingly include multiple measurements of many complementary data types. Here, we present HAllA, a method and implementation that overcomes the statistical challenges presented by data of this type by using feature similarity within each dataset to find statistically significant groups of features between them. We applied HAllA to simulated and real datasets, showing that HAllA outperformed existing procedures and identified compelling biological relationships. HAllA is widely applicable to diverse data structures and presents the user with grouped results that are easier to interpret than traditional methods.

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Bayesian modelling of high-throughput sequencing assays with malacoda

NGS studies have uncovered an ever-growing catalog of human variation while leaving an enormous gap between observed variation and experimental characterization of variant function. High-throughput screens powered by NGS have greatly increased the rate of variant functionalization, but the development of comprehensive statistical methods to analyze screen data has lagged behind. In the massively parallel reporter assay (MPRA), short barcodes are counted by sequencing DNA libraries transfected into cells and output RNA in order to simultaneously measure the shifts in transcription induced by thousands of genetic variants. These counts present many statistical challenges, including over-dispersion, depth dependence, and uncertain DNA concentrations. So far, the statistical methods used have been rudimentary, employing transformations on count level data and disregarding experimental and technical structure while failing to quantify uncertainty in the statistical model.\n\nWe have developed an extensive framework for the analysis of NGS functionalization screens available as an R package called malacoda (available from github.com/andrewGhazi/malacoda). Our software implements a probabilistic, fully Bayesian model of screen data. The model uses the negative binomial distribution with gamma priors to model sequencing counts while accounting for effects from input library preparation and sequencing depth. The method leverages the high-throughput nature of the assay to estimate the priors empirically. External annotations such as ENCODE data or DeepSea predictions can also be incorporated to obtain more informative priors - a transformative capability for data integration. The package also includes quality control and utility functions, including automated barcode counting and visualization methods.\n\nTo validate our method, we analyzed several datasets datasets using malacoda and alternative MPRA analysis methods. These data include experiments from the literature, simulated assays, and primary MPRA data. We also used luciferase assays to experimentally validate the strongest hits from our primary data, as well as variants for which the various methods disagree and variants detectable only with the aid of external annotations.\n\nAuthor SummaryGenetic sequencing technology has progressed rapidly in the past two decades. Huge genomic characterization studies have resulted in a massive quantity of background information across the entire genome, including catalogs of observed human variation, gene regulation features, and computational predictions of genomic function. Meanwhile, new types of experiments use the same sequencing technology to simultaneously test the impact of thousands of mutations on gene regulation. While the design of experiments has become increasingly complex, the data analysis methods deployed have remained overly simplistic, often relying on summary measures that discard information. Here we present a statistical framework called for the analysis of massively parallel genomic experiments designed to incorporate prior information in an unbiased way. We validate our method by comparing our method to alternatives on simulated and real datasets, by using different types of assays that provide a similar type of information, and by closely inspecting an example experimental result that only our method detected. We also present the methods accompanying software package which provides and end-to-end pipeline that provides a simple interface for data preparation, analysis, and visualization.

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