Analysis and correction of compositional bias in sparse sequencing count data
Abstract Background Count data derived from high-throughput deoxy-ribonucliec acid (DNA) sequencing is frequently used in quantitative molecular assays. Due to properties inherent to the sequencing process, unnormalized count data is compositional, measuring relative and not absolute abundances of t...
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doaj-07388e3a527746048a5877c7081c3f382020-11-25T01:22:01ZengBMCBMC Genomics1471-21642018-11-0119112310.1186/s12864-018-5160-5Analysis and correction of compositional bias in sparse sequencing count dataM. Senthil Kumar0Eric V. Slud1Kwame Okrah2Stephanie C. Hicks3Sridhar Hannenhalli4Héctor Corrada Bravo5Graduate Program in Bioinformatics, University of MarylandDepartment of Mathematics, University of MarylandGRED Oncology Biostatistics, GenentechBiostatistics and Computational Biology, Dana-Farber Cancer Institute, Harvard UniversityCenter for Bioinformatics and Computational Biology, University of MarylandCenter for Bioinformatics and Computational Biology, University of MarylandAbstract Background Count data derived from high-throughput deoxy-ribonucliec acid (DNA) sequencing is frequently used in quantitative molecular assays. Due to properties inherent to the sequencing process, unnormalized count data is compositional, measuring relative and not absolute abundances of the assayed features. This compositional bias confounds inference of absolute abundances. Commonly used count data normalization approaches like library size scaling/rarefaction/subsampling cannot correct for compositional or any other relevant technical bias that is uncorrelated with library size. Results We demonstrate that existing techniques for estimating compositional bias fail with sparse metagenomic 16S count data and propose an empirical Bayes normalization approach to overcome this problem. In addition, we clarify the assumptions underlying frequently used scaling normalization methods in light of compositional bias, including scaling methods that were not designed directly to address it. Conclusions Compositional bias, induced by the sequencing machine, confounds inferences of absolute abundances. We present a normalization technique for compositional bias correction in sparse sequencing count data, and demonstrate its improved performance in metagenomic 16s survey data. Based on the distribution of technical bias estimates arising from several publicly available large scale 16s count datasets, we argue that detailed experiments specifically addressing the influence of compositional bias in metagenomics are needed.http://link.springer.com/article/10.1186/s12864-018-5160-5Compositional biasNormalizationEmpirical BayesData integrationCount dataMetagenomics |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
M. Senthil Kumar Eric V. Slud Kwame Okrah Stephanie C. Hicks Sridhar Hannenhalli Héctor Corrada Bravo |
spellingShingle |
M. Senthil Kumar Eric V. Slud Kwame Okrah Stephanie C. Hicks Sridhar Hannenhalli Héctor Corrada Bravo Analysis and correction of compositional bias in sparse sequencing count data BMC Genomics Compositional bias Normalization Empirical Bayes Data integration Count data Metagenomics |
author_facet |
M. Senthil Kumar Eric V. Slud Kwame Okrah Stephanie C. Hicks Sridhar Hannenhalli Héctor Corrada Bravo |
author_sort |
M. Senthil Kumar |
title |
Analysis and correction of compositional bias in sparse sequencing count data |
title_short |
Analysis and correction of compositional bias in sparse sequencing count data |
title_full |
Analysis and correction of compositional bias in sparse sequencing count data |
title_fullStr |
Analysis and correction of compositional bias in sparse sequencing count data |
title_full_unstemmed |
Analysis and correction of compositional bias in sparse sequencing count data |
title_sort |
analysis and correction of compositional bias in sparse sequencing count data |
publisher |
BMC |
series |
BMC Genomics |
issn |
1471-2164 |
publishDate |
2018-11-01 |
description |
Abstract Background Count data derived from high-throughput deoxy-ribonucliec acid (DNA) sequencing is frequently used in quantitative molecular assays. Due to properties inherent to the sequencing process, unnormalized count data is compositional, measuring relative and not absolute abundances of the assayed features. This compositional bias confounds inference of absolute abundances. Commonly used count data normalization approaches like library size scaling/rarefaction/subsampling cannot correct for compositional or any other relevant technical bias that is uncorrelated with library size. Results We demonstrate that existing techniques for estimating compositional bias fail with sparse metagenomic 16S count data and propose an empirical Bayes normalization approach to overcome this problem. In addition, we clarify the assumptions underlying frequently used scaling normalization methods in light of compositional bias, including scaling methods that were not designed directly to address it. Conclusions Compositional bias, induced by the sequencing machine, confounds inferences of absolute abundances. We present a normalization technique for compositional bias correction in sparse sequencing count data, and demonstrate its improved performance in metagenomic 16s survey data. Based on the distribution of technical bias estimates arising from several publicly available large scale 16s count datasets, we argue that detailed experiments specifically addressing the influence of compositional bias in metagenomics are needed. |
topic |
Compositional bias Normalization Empirical Bayes Data integration Count data Metagenomics |
url |
http://link.springer.com/article/10.1186/s12864-018-5160-5 |
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