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Ensemble analysis of adaptive compressed genome sequencing strategies
BACKGROUND: Acquiring genomes at single-cell resolution has many applications such as in the study of microbiota. However, deep sequencing and assembly of all of millions of cells in a sample is prohibitively costly. A property that can come to rescue is that deep sequencing of every cell should not...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2014
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4221792/ https://www.ncbi.nlm.nih.gov/pubmed/25252999 http://dx.doi.org/10.1186/1471-2105-15-S9-S13 |
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author | Taghavi, Zeinab |
author_facet | Taghavi, Zeinab |
author_sort | Taghavi, Zeinab |
collection | PubMed |
description | BACKGROUND: Acquiring genomes at single-cell resolution has many applications such as in the study of microbiota. However, deep sequencing and assembly of all of millions of cells in a sample is prohibitively costly. A property that can come to rescue is that deep sequencing of every cell should not be necessary to capture all distinct genomes, as the majority of cells are biological replicates. Biologically important samples are often sparse in that sense. In this paper, we propose an adaptive compressed method, also known as distilled sensing, to capture all distinct genomes in a sparse microbial community with reduced sequencing effort. As opposed to group testing in which the number of distinct events is often constant and sparsity is equivalent to rarity of an event, sparsity in our case means scarcity of distinct events in comparison to the data size. Previously, we introduced the problem and proposed a distilled sensing solution based on the breadth first search strategy. We simulated the whole process which constrained our ability to study the behavior of the algorithm for the entire ensemble due to its computational intensity. RESULTS: In this paper, we modify our previous breadth first search strategy and introduce the depth first search strategy. Instead of simulating the entire process, which is intractable for a large number of experiments, we provide a dynamic programming algorithm to analyze the behavior of the method for the entire ensemble. The ensemble analysis algorithm recursively calculates the probability of capturing every distinct genome and also the expected total sequenced nucleotides for a given population profile. Our results suggest that the expected total sequenced nucleotides grows proportional to log of the number of cells and proportional linearly with the number of distinct genomes. The probability of missing a genome depends on its abundance and the ratio of its size over the maximum genome size in the sample. The modified resource allocation method accommodates a parameter to control that probability. AVAILABILITY: The squeezambler 2.0 C++ source code is available at http://sourceforge.net/projects/hyda/. The ensemble analysis MATLAB code is available at http://sourceforge.net/projects/distilled-sequencing/. |
format | Online Article Text |
id | pubmed-4221792 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-42217922014-11-10 Ensemble analysis of adaptive compressed genome sequencing strategies Taghavi, Zeinab BMC Bioinformatics Proceedings BACKGROUND: Acquiring genomes at single-cell resolution has many applications such as in the study of microbiota. However, deep sequencing and assembly of all of millions of cells in a sample is prohibitively costly. A property that can come to rescue is that deep sequencing of every cell should not be necessary to capture all distinct genomes, as the majority of cells are biological replicates. Biologically important samples are often sparse in that sense. In this paper, we propose an adaptive compressed method, also known as distilled sensing, to capture all distinct genomes in a sparse microbial community with reduced sequencing effort. As opposed to group testing in which the number of distinct events is often constant and sparsity is equivalent to rarity of an event, sparsity in our case means scarcity of distinct events in comparison to the data size. Previously, we introduced the problem and proposed a distilled sensing solution based on the breadth first search strategy. We simulated the whole process which constrained our ability to study the behavior of the algorithm for the entire ensemble due to its computational intensity. RESULTS: In this paper, we modify our previous breadth first search strategy and introduce the depth first search strategy. Instead of simulating the entire process, which is intractable for a large number of experiments, we provide a dynamic programming algorithm to analyze the behavior of the method for the entire ensemble. The ensemble analysis algorithm recursively calculates the probability of capturing every distinct genome and also the expected total sequenced nucleotides for a given population profile. Our results suggest that the expected total sequenced nucleotides grows proportional to log of the number of cells and proportional linearly with the number of distinct genomes. The probability of missing a genome depends on its abundance and the ratio of its size over the maximum genome size in the sample. The modified resource allocation method accommodates a parameter to control that probability. AVAILABILITY: The squeezambler 2.0 C++ source code is available at http://sourceforge.net/projects/hyda/. The ensemble analysis MATLAB code is available at http://sourceforge.net/projects/distilled-sequencing/. BioMed Central 2014-09-10 /pmc/articles/PMC4221792/ /pubmed/25252999 http://dx.doi.org/10.1186/1471-2105-15-S9-S13 Text en Copyright © 2014 Taghavi; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Proceedings Taghavi, Zeinab Ensemble analysis of adaptive compressed genome sequencing strategies |
title | Ensemble analysis of adaptive compressed genome sequencing strategies |
title_full | Ensemble analysis of adaptive compressed genome sequencing strategies |
title_fullStr | Ensemble analysis of adaptive compressed genome sequencing strategies |
title_full_unstemmed | Ensemble analysis of adaptive compressed genome sequencing strategies |
title_short | Ensemble analysis of adaptive compressed genome sequencing strategies |
title_sort | ensemble analysis of adaptive compressed genome sequencing strategies |
topic | Proceedings |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4221792/ https://www.ncbi.nlm.nih.gov/pubmed/25252999 http://dx.doi.org/10.1186/1471-2105-15-S9-S13 |
work_keys_str_mv | AT taghavizeinab ensembleanalysisofadaptivecompressedgenomesequencingstrategies |