CONTESSA · COuNt data TimE SerieS Analysis: significance tests and sequencing data application
Horizon 2020 — Marie Skłodowska-Curie Actions
- Duration
- 2015-08-01 → 2017-07-31
- EU contribution
- €195,455
- Participants
- 1
- Scheme
- MSCA-IF-EF-ST
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Results in brief
COuNt data TimE SerieS Analysis: significance tests and sequencing data application
The aim of this project is to develop methods for analysis of time-series based on count data. The target of my project broadens to general analysis of count time-series data such as clustering, classification, perturbations inference and machine learning over sequential count data. The project focus on count data sets from ribonucleic acid sequencing (RNA-seq) time course experiments. My project potentially has promising applications in biology, recent examples include high- throughput sequencing, such as RNA-seq and chromatin immunoprecipitation sequencing (ChIP-seq) analyses and more recently Single Cell sequencing.
Data: CORDIS, © European Union
Project objective
The aim of this project is to develop methods for analysis of time-series based on count data. For example, detecting significant differences between two count data time series would distinguish between two different models: one in which the two time series are interchangeable, and one in which the second sample is a modification of the first, i.e. the two time series are non-interchangeable. This will broaden the target of my project to general analysis of count time-series data such as clustering, classification, perturbations inference and machine learning over sequential count data. The project will focus on count data sets from ribonucleic acid sequencing (RNA-seq) time course experiments. The method I plan to develop potentially has promising applications in a variety of multidisciplinary fields where event-counting is required, such as economics and biology. In economics, examples include the number of applicants for a job, or the number of labour strikes during a year. In biology, recent examples include high-throughput sequencing, such as RNA-seq and chromatin immunoprecipitation sequencing (ChIP-seq) analyses. These examples are especially relevant to this project because the method I will be developing enables various features of organisms to be compared through tag counts.I am enthusiastic about having the opportunity to be instrumental to a field where once developed this project will have areal impact in finding better treatments for patients with neurodegenerative diseases including amyotrophic lateral sclerosis (ALS), Alzheimer’s and Parkinson’s Disease. Professor Neil Lawrence will act as the supervisor of the fellowship and will take over responsibility for my training and development. My fellowship experience will be enriched further through a six month secondment period at University of Manchester with Professor Magnus Rattray and through the opportunity to collaborate with SITraN’s Professor Winston Hide and Biogen Idec Industry.
Original text from CORDIS.
Participants
- THE UNIVERSITY OF SHEFFIELD · SHEFFIELDCoordinatorUnited Kingdom
Links
- View on CORDIS
- DOI: 10.3030/660388
- https://web.archive.org/web/20190722121421/http://www.sheffield.ac.uk/neuroscience/staff/cutillo
Data: CORDIS, © European Union
