A Simple Automated DNA Extraction Method for Dried Blood Specimens Collected on Filter Paper

Journal of Laboratory Automation

Volumn 10, Issue 5, 2005, Pages 310-314

  Lin, Zhili ^a   Suzow, Joseph G ^a   Fontaine, Jamie M ^a   Naylor, Edwin W ^a  

^a PERKINELMER INC   (United States)

Author keywords

automation; DNA extraction; dried blood spot; genotyping; Guthrie card; high throughput; newborn screening

Indexed keywords

BLOOD; FILTERS (FOR FLUIDS); GENES; GENETIC ENGINEERING; METHANOL; PAPER PRODUCTS;

DNA EXTRACTION; DRIED BLOOD SPOT; GUTHRIE CARD; HIGH THROUGHPUT GENOTYPING; NEWBORN SCREENING;

DNA;

GENOMIC DNA; METHANOL; TROMETAMOL;

ARTICLE; BLOOD SAMPLING; CONTROLLED STUDY; COST EFFECTIVENESS ANALYSIS; DNA EXTRACTION; DNA ISOLATION; ECONOMIC ASPECT; FILTER; GENOTYPE; HIGH THROUGHPUT SCREENING; HUMAN; LABORATORY AUTOMATION; NEWBORN SCREENING; POLYMERASE CHAIN REACTION; ROBOTICS;

BLOOD; FILTER PAPERS; GENES; GENETIC ENGINEERING; METHANOL; NUCLEIC ACIDS; PAPER PRODUCTS;

EID: 27644567363     PISSN: 22110682     EISSN: 15402452     Source Type: Journal    
DOI: 10.1016/j.jala.2005.07.004     Document Type: Article

References (14)

1. Guthrie R. Susi A. A simple phenylalanine method for detecting phenylketonuria in large populations of newborn infants. Pediatrics 1963, 32, 338–343.
2. National Newborn Screening and Genetics Resource Center. February 2003. National Newborn Screening Report − 2000. NNSGRC, Austin, TX, http://genes-r-us.uthscsa.edu.
3. Clague A. Thomas A. Neonatal biochemical screening for disease. Clin. Chim. Acta 2002, 315, 99–110.
4. Chace D. H. Kalas T. A. Naylor E. W. The application of tandem mass spectrometry to neonatal screening for inherited disorders of intermediary metabolism. Annu. Rev. Genomics Hum. Genet 2002, 3, 17–45.
5. Black J. An isoelectricfocusing method to detect hemoglobin variants in newborn blood samples including the beta-thalassemias. Hemoglobin 1988, 12, 681–689.
6. Shapira E. Miller V. L. Miller J. B. Qu Y. Sickle cell screening using a rapid automated HPLC system. Clin. Chim. Acta 1989, 182, 301–308.
7. http://www.whatman.com/repository/documents/s7/What8168.pdf.
8. Heath E. M. O'Brien D. P. Banas R. Naylor E. W. Dobrowolski S. Optimization of an automated DNA purification protocol for neonatal screening. Arch. Pathol. Lab. Med 1999, 123, 1154–1160.
9. Lin Z. Suzow J. G. Fontaine J. M. Naylor E. W. A high throughput beta-globin genotyping method by multiplexed melting temperature analysis. Mol. Genet. Metab 2004, 81, 237–243.
10. Hannon W. H. Aziz K. J. Collier F. C. Fisher D. A. Blood collection on filter paper for neonatal screening programs. 2nd edition. National Committee for Clinical Laboratory Standards: Villanova, PA; 1992; 1.
11. Johansson P. J. Jonsson M. Ahlfors K. Ivarsson S. A. Svanberg L. Guthenberg C. Retrospective diagnostics of congenital cytomegalovirus infection performed by polymerase chain reaction in blood stored on filter paper. Scand. J. Infect. Dis 1997, 29, 465–468.
12. Kline M. C. Duewer D. L. Redman J. W. Butler J. M. Boyer D. A. Polymerase chain reaction amplification of DNA from aged blood stains: Quantitative evaluation of the “suitability for purpose” of four filter papers as archival media. Anal. Chem 2002, 74, 1863–1869.
13. Makowski G. S. Davis E. L. Hopfer S. M. The effect of storage on Guthrie cards: Implications for deoxyribonucleic acid amplification. Ann. Clin. Lab. Sci 1996, 26, 458–469.
14. Brambilla D. Jennings C. Aldrovandi G. Bremer J. Comeau A. M. Cassol S. A. Multicenter evaluation of use of dried blood and plasma spot specimens in quantitative assays for human immunodeficiency virus RNA: Measurement, precision, and RNA stability. J. Clin. Microbiol 2003, 41, 1888–1893.