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SequencErr: measuring and suppressing sequencer errors in next-generation sequencing data
by
Ren, Dongren
, Shaner, Bridget
, Robison, Leslie L.
, Shao, Ying
, Liu, Yanling
, Pounds, Stanley
, Gout, Alexander M.
, Ma, Xiaotu
, Rice, Stephen V.
, Nakitandwe, Joy
, Easton, John
, Sun, Yu
, Davis, Eric M.
, Szlachta, Karol
, Hall, Salina
, Klco, Jeffery M.
, Wang, Zhaoming
, Mulder, Heather L.
, Kolekar, Pandurang
in
Accuracy
/ Algorithms
/ Animal Genetics and Genomics
/ Bioinformatics
/ Biomedical and Life Sciences
/ Calibration
/ Computer applications
/ data collection
/ Datasets
/ Deoxyribonucleic acid
/ DNA
/ DNA libraries
/ DNA sequencing
/ Error suppression
/ Evolutionary Biology
/ Gene Library
/ genome
/ High-Throughput Nucleotide Sequencing - methods
/ Human Genetics
/ Humans
/ Life Sciences
/ Microbial Genetics and Genomics
/ Models, Genetic
/ Mutation
/ Next-generation sequencing
/ Nucleotide sequence
/ Plant Genetics and Genomics
/ Quality control
/ SARS-CoV-2
/ Sequence Analysis, DNA - methods
/ Sequencer/instrument error
2021
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SequencErr: measuring and suppressing sequencer errors in next-generation sequencing data
by
Ren, Dongren
, Shaner, Bridget
, Robison, Leslie L.
, Shao, Ying
, Liu, Yanling
, Pounds, Stanley
, Gout, Alexander M.
, Ma, Xiaotu
, Rice, Stephen V.
, Nakitandwe, Joy
, Easton, John
, Sun, Yu
, Davis, Eric M.
, Szlachta, Karol
, Hall, Salina
, Klco, Jeffery M.
, Wang, Zhaoming
, Mulder, Heather L.
, Kolekar, Pandurang
in
Accuracy
/ Algorithms
/ Animal Genetics and Genomics
/ Bioinformatics
/ Biomedical and Life Sciences
/ Calibration
/ Computer applications
/ data collection
/ Datasets
/ Deoxyribonucleic acid
/ DNA
/ DNA libraries
/ DNA sequencing
/ Error suppression
/ Evolutionary Biology
/ Gene Library
/ genome
/ High-Throughput Nucleotide Sequencing - methods
/ Human Genetics
/ Humans
/ Life Sciences
/ Microbial Genetics and Genomics
/ Models, Genetic
/ Mutation
/ Next-generation sequencing
/ Nucleotide sequence
/ Plant Genetics and Genomics
/ Quality control
/ SARS-CoV-2
/ Sequence Analysis, DNA - methods
/ Sequencer/instrument error
2021
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SequencErr: measuring and suppressing sequencer errors in next-generation sequencing data
by
Ren, Dongren
, Shaner, Bridget
, Robison, Leslie L.
, Shao, Ying
, Liu, Yanling
, Pounds, Stanley
, Gout, Alexander M.
, Ma, Xiaotu
, Rice, Stephen V.
, Nakitandwe, Joy
, Easton, John
, Sun, Yu
, Davis, Eric M.
, Szlachta, Karol
, Hall, Salina
, Klco, Jeffery M.
, Wang, Zhaoming
, Mulder, Heather L.
, Kolekar, Pandurang
in
Accuracy
/ Algorithms
/ Animal Genetics and Genomics
/ Bioinformatics
/ Biomedical and Life Sciences
/ Calibration
/ Computer applications
/ data collection
/ Datasets
/ Deoxyribonucleic acid
/ DNA
/ DNA libraries
/ DNA sequencing
/ Error suppression
/ Evolutionary Biology
/ Gene Library
/ genome
/ High-Throughput Nucleotide Sequencing - methods
/ Human Genetics
/ Humans
/ Life Sciences
/ Microbial Genetics and Genomics
/ Models, Genetic
/ Mutation
/ Next-generation sequencing
/ Nucleotide sequence
/ Plant Genetics and Genomics
/ Quality control
/ SARS-CoV-2
/ Sequence Analysis, DNA - methods
/ Sequencer/instrument error
2021
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SequencErr: measuring and suppressing sequencer errors in next-generation sequencing data
Journal Article
SequencErr: measuring and suppressing sequencer errors in next-generation sequencing data
2021
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Overview
Background
There is currently no method to precisely measure the errors that occur in the sequencing instrument/sequencer, which is critical for next-generation sequencing applications aimed at discovering the genetic makeup of heterogeneous cellular populations.
Results
We propose a novel computational method, SequencErr, to address this challenge by measuring the base correspondence between overlapping regions in forward and reverse reads. An analysis of 3777 public datasets from 75 research institutions in 18 countries revealed the sequencer error rate to be ~ 10 per million (pm) and 1.4% of sequencers and 2.7% of flow cells have error rates > 100 pm. At the flow cell level, error rates are elevated in the bottom surfaces and > 90% of HiSeq and NovaSeq flow cells have at least one outlier error-prone tile. By sequencing a common DNA library on different sequencers, we demonstrate that sequencers with high error rates have reduced overall sequencing accuracy, and removal of outlier error-prone tiles improves sequencing accuracy. We demonstrate that SequencErr can reveal novel insights relative to the popular quality control method FastQC and achieve a 10-fold lower error rate than popular error correction methods including Lighter and Musket.
Conclusions
Our study reveals novel insights into the nature of DNA sequencing errors incurred on DNA sequencers. Our method can be used to assess, calibrate, and monitor sequencer accuracy, and to computationally suppress sequencer errors in existing datasets.
Publisher
BioMed Central,Springer Nature B.V,BMC
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