Assessment of PHRED Score Characteristics in Illumina MiSeq Amplicon Sequencing.
Supporting Files
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April 7, 2026
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Available in CDC Stacks on April 07, 2026, 12:00 AM
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English
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Alternative Title:Journal of Computational Biology : A Journal of Computational Molecular Cell Biology, 2026, v. 33, no. 56: Assessment of PHRED Score Characteristics in Illumina MiSeq Amplicon Sequencing.
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Journal Article:Journal of Computational Biology : A Journal of Computational Molecular Cell Biology
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Personal Author:
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Description:PHRED scores are confidence values associated with each basecall generated by sequencers. The score is defined as a monotonic function of the probability that the basecall is incorrect. The calibration of PHRED scores has previously been examined by evaluating errors made in reading known sequences. We investigated the calibration of the Illumina MiSeq instrument PHRED model using data from a large dataset. We also derive calibration methods for the PHRED scores in datasets similar to those produced by the Global Hepatitis Outbreak and Surveillance Technology (GHOST). The GHOST protocol uses a short amplicon, resulting in many positions having two base calls, one coming from each of the paired reads. A maximum likelihood model of redundant base calls that match each other was used to estimate corrected probabilities of the PHRED scores. The PHRED scores showed only small absolute deviations from their target values. These differences are statistically significant deviations (
) from being calibrated. The accuracy of the scores varied significantly between the MiSeq instrument runs. Recalibration produced quality scores that improved Brier scores for the dataset by an average relative improvement of
. Methods developed to create calibration curves for PHRED scores will be useful in improving error-correction pipelines based on redundant deep sequencing of amplicon data. However, quality scores are relatively uninformative of substitution errors. The quality scores assigned are determined more by the global error rate of the sequencing run in the current machine cycle than by the characteristics of the specific base call. -
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Source:Journal of Computational Biology : A Journal of Computational Molecular Cell Biology, 2026, v. 33, no. 56
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DOI:
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ISSN:1066-5277 ; 1557-8666
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Pubmed ID:41902738
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Pubmed Central ID:PMC13051658
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Pages in Document:705-715 (19 pdf pages)
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Volume:33
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Issue:56
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Main Document Checksum:urn:sha-512:5873fde4aef49fd4b4bc22c436ecc6817a264fc73bda8a450406da7dcb4ff6e64f3086358623d79b220f7076e376940a65e901d5160815bfd34ef950089d23a9
Supporting Files
File Language:
English
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