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New methods for analyzing serological data with applications to influenza surveillance

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TLDR
In this article, log-transformed serological data (obtained from the hemagglutination-inhibition assay) exist in an effectively one-dimensional space, and computational methods are developed for accurately and efficiently recovering unmeasured serology data from a sample of measured data, and systematically minimizing noise found in the measured data.
Abstract
Two important challenges to the use of serological assays for influenza surveillance include the substantial amount of experimental effort involved, and the inherent noisiness of serological data. Here, informed by the observation that log-transformed serological data (obtained from the hemagglutination-inhibition assay) exist in an effectively one-dimensional space, computational methods are developed for accurately and efficiently recovering unmeasured serological data from a sample of measured data, and systematically minimizing noise found in the measured data. Careful application of these methods would enable the collection of better-quality serological data on a greater number of circulating influenza viruses than is currently possible, and improve the ability to identify potential epidemic/pandemic viruses before they become widespread. Although the focus here is on influenza surveillance, the described methods are more widely applicable.

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Citations
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Single Hemagglutinin Mutations that Alter Both Antigenicity and Receptor Binding Avidity Influence Influenza Virus Antigenic Clustering

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Effects of egg-adaptation on receptor-binding and antigenic properties of recent influenza A (H3N2) vaccine viruses

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Inference of genotype-phenotype relationships in the antigenic evolution of human influenza A (H3N2) viruses.

TL;DR: This work has developed a method for inferring ‘antigenic trees’ for the major viral surface protein hemagglutinin and identified both known and novel sites, and amino acid changes with antigenic impact in the evolution of influenza A (H3N2) viruses from 1968 to 2003.
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Predicting Antigenicity of Influenza A Viruses Using biophysical ideas.

TL;DR: This study presents a simple and physically interpretable model that can predict antigenic relationships among influenza A viruses, based on biophysical ideas, using both genomic amino acid sequences and experimental antigenic data.
References
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A Simple Sequentially Rejective Multiple Test Procedure

TL;DR: In this paper, a simple and widely accepted multiple test procedure of the sequentially rejective type is presented, i.e. hypotheses are rejected one at a time until no further rejections can be done.
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Exact Matrix Completion via Convex Optimization

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Antigenic and Genetic Characteristics of Swine-Origin 2009 A(H1N1) Influenza Viruses Circulating in Humans

Rebecca Garten, +62 more
- 10 Jul 2009 - 
TL;DR: The lack of similarity between the 2009 A(H1N1) virus and its nearest relatives indicates that its gene segments have been circulating undetected for an extended period as mentioned in this paper.
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Origins and evolutionary genomics of the 2009 swine-origin H1N1 influenza A epidemic.

TL;DR: It is shown that the new swine-origin influenza A (H1N1) virus emerged in Mexico and the United States was derived from several viruses circulating in swine, and that the initial transmission to humans occurred several months before recognition of the outbreak.
Journal ArticleDOI

Mapping the Antigenic and Genetic Evolution of Influenza Virus

TL;DR: The antigenic evolution of influenza A (H3N2) virus was quantified and visualized from its introduction into humans in 1968 to 2003 and offers a route to predicting the relative success of emerging strains.
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