182 related articles for article (PubMed ID: 37812635)
1. A novel metric to improve mismatched primer selection and quantification accuracy in amplifying DNA repeats for quantitative polymerase chain reactions.
Xu EY; Schneper LM; Notterman DA
PLoS One; 2023; 18(10):e0292559. PubMed ID: 37812635
[TBL] [Abstract][Full Text] [Related]
2. Deconstructing the polymerase chain reaction: understanding and correcting bias associated with primer degeneracies and primer-template mismatches.
Green SJ; Venkatramanan R; Naqib A
PLoS One; 2015; 10(5):e0128122. PubMed ID: 25996930
[TBL] [Abstract][Full Text] [Related]
3. The effect of multiple primer-template mismatches on quantitative PCR accuracy and development of a multi-primer set assay for accurate quantification of pcrA gene sequence variants.
Ledeker BM; De Long SK
J Microbiol Methods; 2013 Sep; 94(3):224-31. PubMed ID: 23806694
[TBL] [Abstract][Full Text] [Related]
4. Single-nucleotide polymorphisms and other mismatches reduce performance of quantitative PCR assays.
Lefever S; Pattyn F; Hellemans J; Vandesompele J
Clin Chem; 2013 Oct; 59(10):1470-80. PubMed ID: 24014836
[TBL] [Abstract][Full Text] [Related]
5. Evaluation of the impact of single nucleotide polymorphisms and primer mismatches on quantitative PCR.
Boyle B; Dallaire N; MacKay J
BMC Biotechnol; 2009 Aug; 9():75. PubMed ID: 19715565
[TBL] [Abstract][Full Text] [Related]
6. Missing the Match Might Not Cost You the Game: Primer-Template Mismatches Studied in Different Hepatitis A Virus Variants.
Persson S; Karlsson M; Borsch-Reniers H; Ellström P; Eriksson R; Simonsson M
Food Environ Virol; 2019 Sep; 11(3):297-308. PubMed ID: 31004336
[TBL] [Abstract][Full Text] [Related]
7. Assessment of primer/template mismatch effects on real-time PCR amplification of target taxa for GMO quantification.
Ghedira R; Papazova N; Vuylsteke M; Ruttink T; Taverniers I; De Loose M
J Agric Food Chem; 2009 Oct; 57(20):9370-7. PubMed ID: 19778057
[TBL] [Abstract][Full Text] [Related]
8. Hemi-nested touchdown PCR combined with primer-template mismatch PCR for rapid isolation and sequencing of low molecular weight glutenin subunit gene family from a hexaploid wheat BAC library.
Huang XQ; Cloutier S
BMC Genet; 2007 May; 8():18. PubMed ID: 17480230
[TBL] [Abstract][Full Text] [Related]
9. The Use of Degenerate Primers in qPCR Analysis of Functional Genes Can Cause Dramatic Quantification Bias as Revealed by Investigation of nifH Primer Performance.
Gaby JC; Buckley DH
Microb Ecol; 2017 Oct; 74(3):701-708. PubMed ID: 28389727
[TBL] [Abstract][Full Text] [Related]
10. A prolific and robust whole-genome genotyping method using PCR amplification via primer-template mismatched annealing.
Zhao S; Zhang C; Wang L; Luo M; Zhang P; Wang Y; Malik WA; Wang Y; Chen P; Qiu X; Wang C; Lu H; Xiang Y; Liu Y; Ruan J; Qian Q; Zhi H; Chang Y
J Integr Plant Biol; 2023 Mar; 65(3):633-645. PubMed ID: 36269601
[TBL] [Abstract][Full Text] [Related]
11. Primers to highly conserved elements optimized for qPCR-based telomere length measurement in vertebrates.
Hudon SF; Palencia Hurtado E; Beck JD; Burden SJ; Bendixsen DP; Callery KR; Sorensen Forbey J; Waits LP; Miller RA; Nielsen ÓK; Heath JA; Hayden EJ
Mol Ecol Resour; 2021 Jan; 21(1):59-67. PubMed ID: 32762107
[TBL] [Abstract][Full Text] [Related]
12. Design factors that influence PCR amplification success of cross-species primers among 1147 mammalian primer pairs.
Housley DJ; Zalewski ZA; Beckett SE; Venta PJ
BMC Genomics; 2006 Oct; 7():253. PubMed ID: 17029642
[TBL] [Abstract][Full Text] [Related]
13. [Polymerase chain reaction, cold probes and clinical diagnosis].
Haras D; Amoros JP
Sante; 1994; 4(1):43-52. PubMed ID: 7909267
[TBL] [Abstract][Full Text] [Related]
14. Enzymological description of multitemplate PCR-Shrinking amplification bias by optimizing the polymerase-template ratio.
Ingr M; Dostál J; Majerová T
J Theor Biol; 2015 Oct; 382():178-86. PubMed ID: 26164060
[TBL] [Abstract][Full Text] [Related]
15. Effect of single mismatches at 3'-end of primers on polymerase chain reaction.
Simsek M; Adnan H
J Sci Res Med Sci; 2000 Jan; 2(1):11-4. PubMed ID: 24019700
[TBL] [Abstract][Full Text] [Related]
16. Quantification of the detrimental effect of a single primer-template mismatch by real-time PCR using the 16S rRNA gene as an example.
Bru D; Martin-Laurent F; Philippot L
Appl Environ Microbiol; 2008 Mar; 74(5):1660-3. PubMed ID: 18192413
[TBL] [Abstract][Full Text] [Related]
17. The effects of internal primer-template mismatches on RT-PCR: HIV-1 model studies.
Christopherson C; Sninsky J; Kwok S
Nucleic Acids Res; 1997 Feb; 25(3):654-8. PubMed ID: 9016609
[TBL] [Abstract][Full Text] [Related]
18. A primer design strategy for PCR amplification of GC-rich DNA sequences.
Li LY; Li Q; Yu YH; Zhong M; Yang L; Wu QH; Qiu YR; Luo SQ
Clin Biochem; 2011 Jun; 44(8-9):692-8. PubMed ID: 21315705
[TBL] [Abstract][Full Text] [Related]
19. The effect of primer-template mismatches on the detection and quantification of nucleic acids using the 5' nuclease assay.
Stadhouders R; Pas SD; Anber J; Voermans J; Mes TH; Schutten M
J Mol Diagn; 2010 Jan; 12(1):109-17. PubMed ID: 19948821
[TBL] [Abstract][Full Text] [Related]
20. The Effect of Single Mismatches on Primer Extension.
Rejali NA; Moric E; Wittwer CT
Clin Chem; 2018 May; 64(5):801-809. PubMed ID: 29444902
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
