Design and analytical validation of clinical DNA sequencing assays
- PMID: 22208486
- DOI: 10.5858/arpa.2010-0623-OA
Design and analytical validation of clinical DNA sequencing assays
Abstract
Context: DNA sequencing is the method of choice for mutation detection in many genes.
Objectives: To demonstrate the analytical accuracy and reliability of DNA sequencing assays developed in clinical laboratories. Only general guidelines exist for the validation of these tests. We provide examples of assay validation strategies for DNA sequencing tests.
Design: We discuss important design and validation considerations.
Results: The validation examples include an accuracy study to evaluate concordance between results obtained by the newly designed assay and analyzed by another method or laboratory. Precision (reproducibility) studies are performed to determine the robustness of the assay. To assess the quality of sequencing assays, several sequence quality measures are available. In addition, assessing the ability of primers to specifically and robustly amplify target regions before sequencing is important.
Conclusion: Protocols for validation of laboratory-developed sequencing assays may vary between laboratories. An example summary of a validation is provided.
Similar articles
-
Validation of fluorescence in situ hybridization using an analyte-specific reagent for detection of abnormalities involving the mixed lineage leukemia gene.Arch Pathol Lab Med. 2012 Jan;136(1):47-52. doi: 10.5858/arpa.2010-0645-SA. Arch Pathol Lab Med. 2012. PMID: 22208487
-
Molecular classification of patients with unexplained hamartomatous and hyperplastic polyposis.JAMA. 2005 Nov 16;294(19):2465-73. doi: 10.1001/jama.294.19.2465. JAMA. 2005. PMID: 16287957
-
Validation of KRAS testing for anti-EGFR therapeutic decisions for patients with metastatic colorectal carcinoma.Arch Pathol Lab Med. 2012 Jan;136(1):26-32. doi: 10.5858/arpa.2011-0220-OA. Arch Pathol Lab Med. 2012. PMID: 22208484
-
[Familial breast cancer, ovarian cancer].Nihon Rinsho. 2006 Jun 28;Suppl 2:366-70. Nihon Rinsho. 2006. PMID: 16817423 Review. Japanese. No abstract available.
-
[Cowden syndrome can be a challenging diagnosis].Ugeskr Laeger. 2014 Jan 20;176(2):162-5. Ugeskr Laeger. 2014. PMID: 24629684 Review. Danish.
Cited by
-
Validation of high throughput sequencing and microbial forensics applications.Investig Genet. 2014 Jul 30;5:9. doi: 10.1186/2041-2223-5-9. eCollection 2014. Investig Genet. 2014. PMID: 25101166 Free PMC article. Review.
-
The role of replicates for error mitigation in next-generation sequencing.Nat Rev Genet. 2014 Jan;15(1):56-62. doi: 10.1038/nrg3655. Epub 2013 Dec 10. Nat Rev Genet. 2014. PMID: 24322726 Free PMC article. Review.
-
MycoSNP: A Portable Workflow for Performing Whole-Genome Sequencing Analysis of Candida auris.Methods Mol Biol. 2022;2517:215-228. doi: 10.1007/978-1-0716-2417-3_17. Methods Mol Biol. 2022. PMID: 35674957
-
Novel Tetra-Primer ARMS-PCR Assays for Thiopurine Intolerance Susceptibility Mutations NUDT15 c.415C>T and TPMT c.719A>G (TPMT*3C) in East Asians.Genes (Basel). 2017 Oct 23;8(10):285. doi: 10.3390/genes8100285. Genes (Basel). 2017. PMID: 29065511 Free PMC article.
-
Analytical Validation and Application of a Targeted Next-Generation Sequencing Mutation-Detection Assay for Use in Treatment Assignment in the NCI-MPACT Trial.J Mol Diagn. 2016 Jan;18(1):51-67. doi: 10.1016/j.jmoldx.2015.07.006. Epub 2015 Nov 18. J Mol Diagn. 2016. PMID: 26602013 Free PMC article. Clinical Trial.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources