National Ict Australia Limited

Nicta Ipr Pty Limited

Adam Kowalczyk

Justin Bedo

Trevor Anderson

Sarah Dods

Kenneth Paul Clarke

Benjamin William Goudey

Eder Kikianty

Karin Klotzbuecher

A computer method of detecting interacting DNA loci by constructing a contingency table from samples of a first trait and samples of a second trait. The samples of the first and second trait are associated with one of a plurality of genotype calls, each relating to an interaction between multiple DNA loci. The contingency table includes frequencies of each genotype call in the samples. Based on the contingency table, measuring the association between the plurality of genotype calls and the first and second traits. Classifying the genotype calls into a first group that is statistically associated with the first trait and a second group that is statistically associated with the second trait.

Identifying interacting DNA loci using a contingency table, classification rules and statistical significance

This disclosure is related to further approximating multiple data vectors of a dataset. The multiple data vectors are initially approximated by one or more stored principle components. A processor performs multiple iterations of determining an updated estimate of a further principle component based on the multiple data vectors that are initially approximated by the one or more stored principle components. The processor performs this step such that the updated estimate of the further principal component further approximates the dataset. In each iteration the processor constrains the updated estimate of the further principal component to be orthogonal to each of the one or more stored principal components. The data vectors of the dataset are not manipulated but remain the same data vectors that are approximated by the stored principal components.

Fast PCA method for big discrete data

A method of assessing a signal to identify particular signal characteristics comprises application of machine learning to multi-dimensional histograms derived from multi-tap sampling of the signal. The signal is sampled from at least two tap points to retrieve a sample set, and the at least two tap points are adapted to retrieve distinct samples from the signal, such as time spaced samples or spectrally distinct samples. Multiple sample sets are retrieved from the signal over time. The at least two dimensional histogram is built from the joint probability distribution of the plurality of sample sets. A machine learning algorithm then processes the multi-dimensional histogram, and is trained to predict a value of at least one characteristic of the signal.

Method and apparatus for automated identification of signal characteristics

Monitoring an optical signal comprises sampling the optical signal from two or more distinct tap points to retrieve a sample set. Multiple such sample sets are obtained over time. A joint probability distribution or phase portrait of the sample sets is assessed for indications of optical signal quality. The tap distinction can be polarization, for example to determine OSNR, or frequency. The tap distinction can be a time delay, which can enable diagnostic differentiation between multiple impairments, such as OSNR, dispersion, PMD, jitter, Q, and the like. Machine learning algorithms are particularly suitable for such diagnosis, particularly when provided a two dimensional histogram of sample density in the phase portrait.

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Glen Waverly, Australia

Adam Kowalczyk