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Items: 1 to 20 of 92

1.

Novel approach for deriving genome wide SNP analysis data from archived blood spots.

Fowler KE, Reitter CP, Walling GA, Griffin DK.

BMC Res Notes. 2012 Sep 13;5:503. doi: 10.1186/1756-0500-5-503.

2.

Robustness of genome-wide scanning using archived dried blood spot samples as a DNA source.

Hollegaard MV, Grove J, Grauholm J, Kreiner-Møller E, Bønnelykke K, Nørgaard M, Benfield TL, Nørgaard-Pedersen B, Mortensen PB, Mors O, Sørensen HT, Harboe ZB, Børglum AD, Demontis D, Ørntoft TF, Bisgaard H, Hougaard DM.

BMC Genet. 2011 Jul 4;12:58. doi: 10.1186/1471-2156-12-58.

3.

A simple non-enzymatic method for the preparation of white spot syndrome virus (WSSV) DNA from the haemolymph of Marsupenaeus japonicus using FTA matrix cards.

Sudhakaran R, Mekata T, Kono T, Supamattaya K, Linh NT, Suzuki Y, Sakai M, Itami T.

J Fish Dis. 2009 Jul;32(7):611-7. doi: 10.1111/j.1365-2761.2009.01042.x.

PMID:
19476557
4.

Long-term storage and safe retrieval of DNA from microorganisms for molecular analysis using FTA matrix cards.

Rajendram D, Ayenza R, Holder FM, Moran B, Long T, Shah HN.

J Microbiol Methods. 2006 Dec;67(3):582-92.

PMID:
16859786
5.

Successful application of FTA Classic Card technology and use of bacteriophage phi29 DNA polymerase for large-scale field sampling and cloning of complete maize streak virus genomes.

Owor BE, Shepherd DN, Taylor NJ, Edema R, Monjane AL, Thomson JA, Martin DP, Varsani A.

J Virol Methods. 2007 Mar;140(1-2):100-5.

PMID:
17174409
6.

Whole genome amplification and real-time PCR in forensic casework.

Giardina E, Pietrangeli I, Martone C, Zampatti S, Marsala P, Gabriele L, Ricci O, Solla G, Asili P, Arcudi G, Spinella A, Novelli G.

BMC Genomics. 2009 Apr 14;10:159. doi: 10.1186/1471-2164-10-159.

7.

Accuracy of multiplexed Illumina platform-based single-nucleotide polymorphism genotyping compared between genomic and whole genome amplified DNA collected from multiple sources.

Paynter RA, Skibola DR, Skibola CF, Buffler PA, Wiemels JL, Smith MT.

Cancer Epidemiol Biomarkers Prev. 2006 Dec;15(12):2533-6.

8.

Whole genome amplification on DNA from filter paper blood spot samples: an evaluation of selected systems.

Sørensen KM, Jespersgaard C, Vuust J, Hougaard D, Nørgaard-Pedersen B, Andersen PS.

Genet Test. 2007 Spring;11(1):65-71.

PMID:
17394394
9.

Laser capture microdissection (LCM) and whole genome amplification (WGA) of DNA from normal breast tissue --- optimization for genome wide array analyses.

Aaltonen KE, Ebbesson A, Wigerup C, Hedenfalk I.

BMC Res Notes. 2011 Mar 18;4:69. doi: 10.1186/1756-0500-4-69.

10.

Improved technique that allows the performance of large-scale SNP genotyping on DNA immobilized by FTA technology.

He H, Argiro L, Dessein H, Chevillard C.

Infect Genet Evol. 2007 Jan;7(1):128-32.

PMID:
16920406
11.

The utility and limitation of single nucleotide polymorphism analysis on whole genome amplified mesenchymal tumour DNA in formalin fixed tumour samples.

Liang CW, Lee YS, Marino-Enriquez A, Tsui K, Huang SH.

Pathology. 2012 Jan;44(1):33-41. doi: 10.1097/PAT.0b013e32834e411e.

PMID:
22157688
12.

Assessment of DNA extracted from FTA cards for use on the Illumina iSelect BeadChip.

McClure MC, McKay SD, Schnabel RD, Taylor JF.

BMC Res Notes. 2009 Jun 16;2:107. doi: 10.1186/1756-0500-2-107.

13.

SNP genotyping on a genome-wide amplified DOP-PCR template.

Grant SF, Steinlicht S, Nentwich U, Kern R, Burwinkel B, Tolle R.

Nucleic Acids Res. 2002 Nov 15;30(22):e125.

14.

Genome-wide scans using archived neonatal dried blood spot samples.

Hollegaard MV, Grauholm J, Børglum A, Nyegaard M, Nørgaard-Pedersen B, Ørntoft T, Mortensen PB, Wiuf C, Mors O, Didriksen M, Thorsen P, Hougaard DM.

BMC Genomics. 2009 Jul 4;10:297. doi: 10.1186/1471-2164-10-297.

15.

Assessing the utility of whole-genome amplified serum DNA for array-based high throughput genotyping.

Bucasas KL, Pandya GA, Pradhan S, Fleischmann RD, Peterson SN, Belmont JW.

BMC Genet. 2009 Dec 18;10:85. doi: 10.1186/1471-2156-10-85.

16.

High quality genome-wide genotyping from archived dried blood spots without DNA amplification.

St Julien KR, Jelliffe-Pawlowski LL, Shaw GM, Stevenson DK, O'Brodovich HM, Krasnow MA; Stanford BPD Study Group..

PLoS One. 2013 May 30;8(5):e64710. doi: 10.1371/journal.pone.0064710.

17.

Comparison of buccal and blood-derived canine DNA, either native or whole genome amplified, for array-based genome-wide association studies.

Rincon G, Tengvall K, Belanger JM, Lagoutte L, Medrano JF, André C, Thomas A, Lawley CT, Hansen MS, Lindblad-Toh K, Oberbauer AM.

BMC Res Notes. 2011 Jun 30;4:226. doi: 10.1186/1756-0500-4-226.

18.

Canine DNA subjected to whole genome amplification is suitable for a wide range of molecular applications.

Short AD, Kennedy LJ, Forman O, Barnes A, Fretwell N, Wiggall R, Thomson W, Ollier WE.

J Hered. 2005;96(7):829-35.

PMID:
16267167
19.

Simple and rapid detection of the porcine reproductive and respiratory syndrome virus from pig whole blood using filter paper.

Inoue R, Tsukahara T, Sunaba C, Itoh M, Ushida K.

J Virol Methods. 2007 Apr;141(1):102-6.

PMID:
17188757
20.

The use of FTA cards for preserving unfixed cytological material for high-throughput molecular analysis.

Saieg MA, Geddie WR, Boerner SL, Liu N, Tsao M, Zhang T, Kamel-Reid S, da Cunha Santos G.

Cancer Cytopathol. 2012 Jun 25;120(3):206-14. doi: 10.1002/cncy.20205.

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