biological interpretation of deepomicsae output using metaboanalyst

Analyse af signalmoduler i Alzheimers sygdom med dyb læring

An increasingly large proportion of the population is aging and the burden of age-related diseases, such as neurodegeneration, is expected to sharply increase in the coming decades1. Alzheimer&#39;s disease is the most common type of neurodegenerative disease2. Progress in finding a treatment has been slow given our poor understanding of the fundamental&#160;molecular mechanisms driving the onset and progress of the disease. The majority of information on Alzheimer&#39;s disease is gained postmortem from the examination of brain tissue, which has made distinguishing causes and consequences a difficult task3. The Religious Orders Study/Memory and Aging Project (ROSMAP) is an ambitious effort to gain a broader understanding of neurodegeneration, which involves the study of thousands of individuals who have committed to undergo medical and psychological examinations yearly and to contribute their brains for research after their demise4. The study focuses on the transition from the normal functioning of the brain to Alzheimer&#39;s disease2. Within the project, postmortem brain samples&#160;were analyzed with a plethora of omics approaches, including genomics, epigenomics, transcriptomics, proteomics5, and metabolomics.
Omics technologies that offer functional readouts of cellular states (i.e., proteomics and metabolomics)6,7 are key to interpreting disease8,9,10,11,12, due to the direct relationship between protein and metabolite abundance and cellular activities. Proteins are the primary executors of cellular processes, while metabolites are the substrates and products for biochemical reactions. Multi-omics data analysis offers the possibility to understand the complex relationships between proteomics and metabolomics data instead of appreciating them in isolation. Multi-omics is a discipline that studies multiple layers of high-dimensional biological data, including molecular data (genome sequence and mutations, transcriptome, proteome, metabolome), clinical imaging data, and clinical features. Particularly, multi-omics data analysis aims to integrate such layers of biological data, understand their reciprocal regulation and interaction dynamics, and deliver a holistic understanding of disease onset and progression. However, methods to integrate multi-omics data remain in the early stages of development13.
Autoencoders, a type of unsupervised neural network14, are a powerful tool for multi-omics data integration. Unlike supervised neural networks, autoencoders do not map samples to specific target values (such as healthy or diseased), nor are they used to predict outcomes. One of their primary applications&#160;lies in dimensionality reduction. However, autoencoders offer several advantages over simpler dimensionality reduction methods such as principal component analysis (PCA), t-distributed stochastic neighbor embedding (tSNE), or uniform manifold approximation and projection (UMAP). Unlike PCA, autoencoders can capture non-linear relationships within the data. Unlike tSNE and UMAP, they can detect hierarchical and multi-modal relationships within the data since they rely on multiple layers of computational units each containing non linear activation functions. Therefore, they represent attractive models to capture the complexity of multi-omics data. Finally, while the primary application of PCA, tSNE, and UMAP is that of clustering the data, autoencoders compress the input data into extracted features that are well-suited for downstream predictive tasks15,16.
Briefly, neural networks comprise several layers, each containing multiple computational units or &#34;neurons.&#34; The first and last layers are referred to as the input and output layers, respectively. Autoencoders are neural networks with an hourglass structure, consisting of an input layer, followed by one to three hidden layers and a small &#34;latent&#34; layer typically containing between two and six neurons. This structure&#39;s first half is known as the encoder and is combined with a decoder mirroring the encoder. The decoder ends with an output layer containing the same number of neurons as the input layer. Autoencoders take the input through the bottleneck and reconstruct it in the output layer, with the goal of generating an output that mirrors the original information as closely as possible. This is achieved by mathematically minimizing a parameter termed &#34;reconstruction loss.&#34; The input consists of a set of features, which in the application showcased herein will be protein and metabolite abundances, and clinical characteristics (i.e., sex, education, and age at death). The latent layer contains a compressed and information-rich representation of the input, which can be used for subsequent applications such as predictive models17,18.
This protocol presents a workflow, DeepOmicsAE, which involves: 1) preprocessing of proteomics, metabolomics, and clinical data (i.e., normalization, scaling, outlier removal) to obtain data with a consistent scale for machine learning analysis; 2) selecting appropriate autoencoder input features, since feature overload may obscure relevant disease patterns; 3) optimizing and training the autoencoder, including determining the optimal number of proteins and metabolites to select, and of neurons for the latent layer; 4) extracting features from the latent layer; and 5) utilizing the extracted features for biological interpretation by identifying molecular signaling modules and their relationship with clinical features.
This protocol aims to be simple and applicable by&#160;biologists with limited computational experience who have a basic understanding of programming with Python. The protocol focuses on analyzing multi-omics data, including proteomics, metabolomics, and clinical features, but its use can be extended to other types of molecular expression data, including transcriptomics. One important novel application introduced by this protocol is mapping the importance scores of original features onto individual neurons in the latent layer. As a result, each neuron in the latent layer represents a signaling module, detailing the interactions between specific molecular alterations and the patients&#39; clinical characteristics. Biological interpretation of the molecular signaling modules is obtained by using MetaboAnalyst, a publicly available tool that integrates gene/protein and metabolite data to derive enriched metabolic and cell signaling pathways17.

Forfatter Spotlight: Fremme af Alzheimers forskning – Udforskning af tidlig opdagelse og multi-omics-tilgange

DeepOmicsAE: Repræsenterer signalmoduler i Alzheimers sygdom med dyb læringsanalyse af proteomics, metabolomics og kliniske data

Alzheimer's disease is thought to initiate decades before symptoms emerge. Recent studies suggest that phenotypic traits such as obesity and hypertension, but also the level of education and social engagement can act as risk factors. Our goal is to become able to decipher their contributions and their relation to molecular drivers of disease to learn how to intervene early and in a personalized manner.Multi-omic data analysis can be used for integrating various layers of biological data such as proteomics, transcriptomics, metabolomics, and phenotypic traits to comprehensively understand a disease state. Autoencoder models use deep learning to reduce the dimensionality of multi-omics datasets, effectively summarizing the crucial information, However, it is challenging to interpret how important are individual features in the original data with respect to the summarized output. In Deep-omics AE, we built in an algorithm that derives the importance of individual multi-omics features relative to the learn reduced dimensionality representation.With this approach, we can identify molecularly similar modules and their association with patient's phenotypic traits. Deep-omics AE helps putting in relation patient's phenotypic traits with the molecular makeup of disease. For example, you can use it to ask, what are the molecular pathways that are most implicated in Alzheimer's disease in older patients, and what are those that are most implicated in younger patients?What are those implicated in developing the disease in less educated patients versus more educated patients?

Biologisk fortolkning af DeepOmicsAE-output ved hjælp af MetaboAnalyst

For at begynde skal du åbne en webbrowser og navigere til linket for at få adgang til Joint Pathway Analysis-funktionaliteten på MetaboAnalyst-webstedet. Få adgang til mappen, hvor outputfilerne fra implementering af DeepOmicsAE gemmes, og åbn tekstfilerne med navnet module_n. txt for hvert genereret signalmodul.Fra tekstfilerne skal du finde listen over proteiner og kopiere dem. På MetaboAnalyst-websiden skal du indsætte den kopierede liste over proteiner i genets proteiner med valgfrit foldeændringsvindue. Gentag for metabolitter, indsæt dem i listen over forbindelser med valgfrit vindue til foldændringer på den samme webside.Vælg den relevante organisme og ID-typen. Indsend derefter oplysningerne ved at klikke på Send nederst på siden. Kontroller id-tilknytningen på den følgende side for at sikre, at id'erne genkendes korrekt, og klik derefter på Fortsæt.På siden Parameterindstilling skal du vælge Integrerede metaboliske veje eller Alle integrerede veje for at visualisere inputtets bidrag til metaboliske eller alle signalveje. I panelet Valg af algoritme skal du vælge Berigelsesanalyse, Hypergeometrisk test; Topologimål, grad centralitet; og integrationsmetode, Kombiner p-værdier pathway-niveau. Klik på Send nederst på siden.Den sidste side, Resultatvisning, viser resultaterne af forbedringsanalysen. Dette omfatter observationsområder med berigede spredningsveje baseret på deres virkning og betydning og en tabelliste over spredningsveje. MetaboAnalyst-fortolkning af signalmodulerne opnået på DeepOmicsAE på et datasæt fra hjerneprøver af raske eller Alzheimers patienter afslørede, at for hvert signalmodul blev forskellige metaboliske og signalveje beriget.Desuden viste karakteriseringen af interaktioner, der forekommer mellem kliniske træk og signalmoduler, at den ændrede glycerolipidmetabolisme hos Alzheimers patienter var forbundet med deres køn og alder ved døden. Omvendt har ændringer af synapser og axonfunktionalitet tendens til at forekomme på tværs af Alzheimers patienter, uanset deres køn, uddannelsesniveau og levetid.

Research

JoVE Journal

Biology

Biological Interpretation of DeepOmicsAE Output Using MetaboAnalyst

DeepOmicsAE: Representing Signaling Modules in Alzheimer's Disease with Deep Learning Analysis of Proteomics, Metabolomics, and Clinical Data

Large omics datasets are becoming increasingly available for research into human health. This paper presents DeepOmicsAE, a workflow optimized for the ...

Data Preprocessing for DeepOmicsAE Workflow

Forbehandling af data til DeepOmicsAE-workflow

Optimizing Model Parameters and Implementing DeepOmicsAE Workflow

Optimering af modelparametre og implementering af DeepOmicsAE workflow