A random forest classifier for detecting rare variants in NGS data from viral populations
We propose a random forest classifier for detecting rare variants from sequencing errors in Next Generation Sequencing (NGS) data from viral populations. The method utilizes counts of varying length of k-mers from the reads of a viral population to train a Random forest classifier, called MultiRes,...
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doaj-488ccf8c5c0747eda49d722525820c6b2020-11-25T01:53:23ZengElsevierComputational and Structural Biotechnology Journal2001-03702017-01-0115388395A random forest classifier for detecting rare variants in NGS data from viral populationsRaunaq Malhotra0Manjari Jha1Mary Poss2Raj Acharya3The School of Electrical Engineering and Computer Science, The Pennsylvania State University, University Park, PA, 16802, USA; Corresponding author.The School of Electrical Engineering and Computer Science, The Pennsylvania State University, University Park, PA, 16802, USADepartment of Biology, The Pennsylvania State University, University Park, PA 16802, USASchool of Informatics and Computing, Indiana University, Bloomington, IN 47405, USAWe propose a random forest classifier for detecting rare variants from sequencing errors in Next Generation Sequencing (NGS) data from viral populations. The method utilizes counts of varying length of k-mers from the reads of a viral population to train a Random forest classifier, called MultiRes, that classifies k-mers as erroneous or rare variants. Our algorithm is rooted in concepts from signal processing and uses a frame-based representation of k-mers. Frames are sets of non-orthogonal basis functions that were traditionally used in signal processing for noise removal. We define discrete spatial signals for genomes and sequenced reads, and show that k-mers of a given size constitute a frame.We evaluate MultiRes on simulated and real viral population datasets, which consist of many low frequency variants, and compare it to the error detection methods used in correction tools known in the literature. MultiRes has 4 to 500 times less false positives k-mer predictions compared to other methods, essential for accurate estimation of viral population diversity and their de-novo assembly. It has high recall of the true k-mers, comparable to other error correction methods. MultiRes also has greater than 95% recall for detecting single nucleotide polymorphisms (SNPs) and fewer false positive SNPs, while detecting higher number of rare variants compared to other variant calling methods for viral populations. The software is available freely from the GitHub link https://github.com/raunaq-m/MultiRes. Keywords: Sequencing error detection, Reference free methods, Next-generation sequencing, Viral populations, Multi-resolution frames, Random forest classifierhttp://www.sciencedirect.com/science/article/pii/S2001037017300399 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Raunaq Malhotra Manjari Jha Mary Poss Raj Acharya |
spellingShingle |
Raunaq Malhotra Manjari Jha Mary Poss Raj Acharya A random forest classifier for detecting rare variants in NGS data from viral populations Computational and Structural Biotechnology Journal |
author_facet |
Raunaq Malhotra Manjari Jha Mary Poss Raj Acharya |
author_sort |
Raunaq Malhotra |
title |
A random forest classifier for detecting rare variants in NGS data from viral populations |
title_short |
A random forest classifier for detecting rare variants in NGS data from viral populations |
title_full |
A random forest classifier for detecting rare variants in NGS data from viral populations |
title_fullStr |
A random forest classifier for detecting rare variants in NGS data from viral populations |
title_full_unstemmed |
A random forest classifier for detecting rare variants in NGS data from viral populations |
title_sort |
random forest classifier for detecting rare variants in ngs data from viral populations |
publisher |
Elsevier |
series |
Computational and Structural Biotechnology Journal |
issn |
2001-0370 |
publishDate |
2017-01-01 |
description |
We propose a random forest classifier for detecting rare variants from sequencing errors in Next Generation Sequencing (NGS) data from viral populations. The method utilizes counts of varying length of k-mers from the reads of a viral population to train a Random forest classifier, called MultiRes, that classifies k-mers as erroneous or rare variants. Our algorithm is rooted in concepts from signal processing and uses a frame-based representation of k-mers. Frames are sets of non-orthogonal basis functions that were traditionally used in signal processing for noise removal. We define discrete spatial signals for genomes and sequenced reads, and show that k-mers of a given size constitute a frame.We evaluate MultiRes on simulated and real viral population datasets, which consist of many low frequency variants, and compare it to the error detection methods used in correction tools known in the literature. MultiRes has 4 to 500 times less false positives k-mer predictions compared to other methods, essential for accurate estimation of viral population diversity and their de-novo assembly. It has high recall of the true k-mers, comparable to other error correction methods. MultiRes also has greater than 95% recall for detecting single nucleotide polymorphisms (SNPs) and fewer false positive SNPs, while detecting higher number of rare variants compared to other variant calling methods for viral populations. The software is available freely from the GitHub link https://github.com/raunaq-m/MultiRes. Keywords: Sequencing error detection, Reference free methods, Next-generation sequencing, Viral populations, Multi-resolution frames, Random forest classifier |
url |
http://www.sciencedirect.com/science/article/pii/S2001037017300399 |
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