Cargando…
Selecting the most appropriate time points to profile in high-throughput studies
Biological systems are increasingly being studied by high throughput profiling of molecular data over time. Determining the set of time points to sample in studies that profile several different types of molecular data is still challenging. Here we present the Time Point Selection (TPS) method that...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5319842/ https://www.ncbi.nlm.nih.gov/pubmed/28124972 http://dx.doi.org/10.7554/eLife.18541 |
_version_ | 1782509436488646656 |
---|---|
author | Kleyman, Michael Sefer, Emre Nicola, Teodora Espinoza, Celia Chhabra, Divya Hagood, James S Kaminski, Naftali Ambalavanan, Namasivayam Bar-Joseph, Ziv |
author_facet | Kleyman, Michael Sefer, Emre Nicola, Teodora Espinoza, Celia Chhabra, Divya Hagood, James S Kaminski, Naftali Ambalavanan, Namasivayam Bar-Joseph, Ziv |
author_sort | Kleyman, Michael |
collection | PubMed |
description | Biological systems are increasingly being studied by high throughput profiling of molecular data over time. Determining the set of time points to sample in studies that profile several different types of molecular data is still challenging. Here we present the Time Point Selection (TPS) method that solves this combinatorial problem in a principled and practical way. TPS utilizes expression data from a small set of genes sampled at a high rate. As we show by applying TPS to study mouse lung development, the points selected by TPS can be used to reconstruct an accurate representation for the expression values of the non selected points. Further, even though the selection is only based on gene expression, these points are also appropriate for representing a much larger set of protein, miRNA and DNA methylation changes over time. TPS can thus serve as a key design strategy for high throughput time series experiments. Supporting Website: www.sb.cs.cmu.edu/TPS DOI: http://dx.doi.org/10.7554/eLife.18541.001 |
format | Online Article Text |
id | pubmed-5319842 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-53198422017-02-23 Selecting the most appropriate time points to profile in high-throughput studies Kleyman, Michael Sefer, Emre Nicola, Teodora Espinoza, Celia Chhabra, Divya Hagood, James S Kaminski, Naftali Ambalavanan, Namasivayam Bar-Joseph, Ziv eLife Computational and Systems Biology Biological systems are increasingly being studied by high throughput profiling of molecular data over time. Determining the set of time points to sample in studies that profile several different types of molecular data is still challenging. Here we present the Time Point Selection (TPS) method that solves this combinatorial problem in a principled and practical way. TPS utilizes expression data from a small set of genes sampled at a high rate. As we show by applying TPS to study mouse lung development, the points selected by TPS can be used to reconstruct an accurate representation for the expression values of the non selected points. Further, even though the selection is only based on gene expression, these points are also appropriate for representing a much larger set of protein, miRNA and DNA methylation changes over time. TPS can thus serve as a key design strategy for high throughput time series experiments. Supporting Website: www.sb.cs.cmu.edu/TPS DOI: http://dx.doi.org/10.7554/eLife.18541.001 eLife Sciences Publications, Ltd 2017-01-26 /pmc/articles/PMC5319842/ /pubmed/28124972 http://dx.doi.org/10.7554/eLife.18541 Text en © 2017, Kleyman et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Computational and Systems Biology Kleyman, Michael Sefer, Emre Nicola, Teodora Espinoza, Celia Chhabra, Divya Hagood, James S Kaminski, Naftali Ambalavanan, Namasivayam Bar-Joseph, Ziv Selecting the most appropriate time points to profile in high-throughput studies |
title | Selecting the most appropriate time points to profile in high-throughput studies |
title_full | Selecting the most appropriate time points to profile in high-throughput studies |
title_fullStr | Selecting the most appropriate time points to profile in high-throughput studies |
title_full_unstemmed | Selecting the most appropriate time points to profile in high-throughput studies |
title_short | Selecting the most appropriate time points to profile in high-throughput studies |
title_sort | selecting the most appropriate time points to profile in high-throughput studies |
topic | Computational and Systems Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5319842/ https://www.ncbi.nlm.nih.gov/pubmed/28124972 http://dx.doi.org/10.7554/eLife.18541 |
work_keys_str_mv | AT kleymanmichael selectingthemostappropriatetimepointstoprofileinhighthroughputstudies AT seferemre selectingthemostappropriatetimepointstoprofileinhighthroughputstudies AT nicolateodora selectingthemostappropriatetimepointstoprofileinhighthroughputstudies AT espinozacelia selectingthemostappropriatetimepointstoprofileinhighthroughputstudies AT chhabradivya selectingthemostappropriatetimepointstoprofileinhighthroughputstudies AT hagoodjamess selectingthemostappropriatetimepointstoprofileinhighthroughputstudies AT kaminskinaftali selectingthemostappropriatetimepointstoprofileinhighthroughputstudies AT ambalavanannamasivayam selectingthemostappropriatetimepointstoprofileinhighthroughputstudies AT barjosephziv selectingthemostappropriatetimepointstoprofileinhighthroughputstudies |