Acta Med. 2012, 55: 160-164
https://doi.org/10.14712/18059694.2015.40
Polyadenylated Sequencing Primers Enable Complete Readability of PCR Amplicons Analyzed by Dideoxynucleotide Sequencing
References
1. M, Hegerová J, Drastíková M. „Alternativní“ biologický materiál pro rutinní analýzu nukleových kyselin – validace preanalytické fáze vyšetření DNA. Klin Biochem Metab 2012; 20: 31–37.
2. J, Gilbert MTP, Campos PF, Willerslev E. 5′-Tailed sequencing primers improve sequencing quality of PCR products. Biotechniques 2007; 42: 174–176.
<https://doi.org/10.2144/000112316>
3. B, Di Luca M, Padovani A. The effect of APOE genotype on clinical phenotype in Alzheimer disease. Neurology 2007; 68: 624.
<https://doi.org/10.1212/01.wnl.0000258354.96336.97>
4. K, Boyle MP, Cheng S, et al. Variants in mannose-binding lectin and tumour necrosis factor alpha affect survival in cystic fibrosis. J Med Genet 2007; 44: 209–214.
<https://doi.org/10.1136/jmg.2006.046318>
<PubMed>
5. JC, Lange C, Raby BA, et al. The transforming growth factor-beta-1 (TGFB1) gene is associated with chronic obstructive pulmonary disease (COPD). Hum Molec Genet 2004; 13: 1649–1656.
<https://doi.org/10.1093/hmg/ddh171>
6. S, Parton M, Dowsett M. The biology of neoadjuvant chemotherapy for breast cancer. Endocr Relat Cancer 2002; 9: 183–95.
<https://doi.org/10.1677/erc.0.0090183>
7. P, van den Maagdenberg AMJM, Stalenhoef AFH, et al. Familial dysbetalipoproteinemia associated with apolipoprotein E3-Leiden in an extended multigeneration pedigree. J Clin Invest 1991; 88: 643–655.
<https://doi.org/10.1172/JCI115349>
<PubMed>
8. R, Akhurst RJ, Balmain A. TGF-beta signaling in tumor suppression and cancer progression. Nature Genet 2001; 29: 117–129.
<https://doi.org/10.1038/ng1001-117>
9. S, Grard G, Brisbarre N, et al. LoPPS: a long PCR product sequencing method for rapid characterisation of long amplicons. Biochem Biophys Res Commun 2006; 344: 1080–1085.
<https://doi.org/10.1016/j.bbrc.2006.04.015>
10. DCS. Alpha-1-antitrypsin deficiency in Europe: geographical distribution of Pi types S and Z. Respir Med 1998; 92: 367–377.
<https://doi.org/10.1016/S0954-6111(98)90278-5>
11. MM, McQuillan MR, O‘Hanlon KA. Second generation sequencing allows for mtDNA mixture deconvolution and high resolution detection of heteroplasmy. Croat Med J 2011; 52: 299–313.
<https://doi.org/10.3325/cmj.2011.52.299>
<PubMed>
12. K, Winchester E, Daly MJ, et al. Large-scale discovery and genotyping of single-nucleotide polymorphisms in the mouse. Nat Genet 2000; 24: 381–6.
<https://doi.org/10.1038/74215>
13. JR, Liu PY, Liu YJ, et al. APOE and TGF-beta-1 genes are associated with obesity phenotypes. J Med Genet 2003; 40: 918–924.
<https://doi.org/10.1136/jmg.40.12.918>
<PubMed>
14. C, Raguenes O, Ferec C. HFE mutations analysis in 711 hemochromatosis probands: evidence for S65C implication in mild form of hemochromatosis. Blood 1999; 93: 2502–2505.
<https://doi.org/10.1182/blood.V93.8.2502>
15. AG, Whatley SD, Morgan RR, Worwood M, Elder GH. Increased frequency of the haemochromatosis cys282tyr mutation in sporadic porphyria cutanea tarda. Lancet 1997; 349: 321–323.
<https://doi.org/10.1016/S0140-6736(96)09436-6>
16. M, Uhlen M, Nyren PA sequencing method based on realtime pyrophosphate. Science 1998; 281: 363–365.
<https://doi.org/10.1126/science.281.5375.363>
17. JJ, Børsting C, Hallenberg C, Buchard A, Hernandez A, Morling N. Multiplex PCR and minisequencing of SNPs – a model with 35 Y chromosome SNPs. Forensic Sci Int 2003; 137: 74–84.
<https://doi.org/10.1016/S0379-0738(03)00299-8>
18. SK, Banerjee PC. Nucleotide sequence analysis of cryptic plasmid pAM5 from Acidiphilium multivorum. Plasmid 2007; 58: 101–114.
<https://doi.org/10.1016/j.plasmid.2007.01.005>
19. KV, Dames S, Durtschi JD. Next generation sequencing for clinical diagnostics – principles and application to targeted resequencing for hypertrophic cardiomyopathy. J Mol Diagn 2010; 12: 539–551.
<https://doi.org/10.2353/jmoldx.2010.100043>
<PubMed>
20. D, Theaker J, Guy SP, Brown T, Little S. Detection of PCR products using self-probing amplicons and fluorescence. Nat Biotechnol 1999; 17: 804–807.
<https://doi.org/10.1038/11751>
21. JT. The molecular etiologies and associated phenotypes of amelogenesis imperfecta. Am J Med Genet 2006; 140A: 2547–2555.
<https://doi.org/10.1002/ajmg.a.31358>
<PubMed>
