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Clin Chem. 2016 Apr;62(4):647-54. doi: 10.1373/clinchem.2015.249623. Epub 2016 Feb 4.

Systematic Evaluation of Sanger Validation of Next-Generation Sequencing Variants.

Author information

1
National Human Genome Research Institute, NIH, Bethesda, MD;
2
National Human Genome Research Institute, NIH, Bethesda, MD; NIH Intramural Sequencing Center, Rockville, MD.
3
National Human Genome Research Institute, NIH, Bethesda, MD; lesb@mail.nih.gov.

Abstract

BACKGROUND:

Next-generation sequencing (NGS) data are used for both clinical care and clinical research. DNA sequence variants identified using NGS are often returned to patients/participants as part of clinical or research protocols. The current standard of care is to validate NGS variants using Sanger sequencing, which is costly and time-consuming.

METHODS:

We performed a large-scale, systematic evaluation of Sanger-based validation of NGS variants using data from the ClinSeq® project. We first used NGS data from 19 genes in 5 participants, comparing them to high-throughput Sanger sequencing results on the same samples, and found no discrepancies among 234 NGS variants. We then compared NGS variants in 5 genes from 684 participants against data from Sanger sequencing.

RESULTS:

Of over 5800 NGS-derived variants, 19 were not validated by Sanger data. Using newly designed sequencing primers, Sanger sequencing confirmed 17 of the NGS variants, and the remaining 2 variants had low quality scores from exome sequencing. Overall, we measured a validation rate of 99.965% for NGS variants using Sanger sequencing, which was higher than many existing medical tests that do not necessitate orthogonal validation.

CONCLUSIONS:

A single round of Sanger sequencing is more likely to incorrectly refute a true-positive variant from NGS than to correctly identify a false-positive variant from NGS. Validation of NGS-derived variants using Sanger sequencing has limited utility, and best practice standards should not include routine orthogonal Sanger validation of NGS variants.

PMID:
26847218
PMCID:
PMC4878677
DOI:
10.1373/clinchem.2015.249623
[Indexed for MEDLINE]
Free PMC Article

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