High-throughput real-time PCR-based genotyping without DNA purification
暂无分享,去创建一个
[1] N. Treff,et al. High-throughput real-time PCR-based genotyping without DNA purification , 2012, BMC Research Notes.
[2] N. Treff,et al. Development of TaqMan allelic discrimination based genotyping of large DNA deletions. , 2012, Genomics.
[3] Victoria Cox,et al. Comparison of Eight Methods for the Extraction of Bacillus atrophaeus Spore DNA from Eleven Common Interferents and a Common Swab , 2011, PloS one.
[4] D. Bowden,et al. Buffy coat specimens remain viable as a DNA source for highly multiplexed genome-wide genetic tests after long term storage , 2011, Journal of Translational Medicine.
[5] N. Treff,et al. Single-cell whole-genome amplification technique impacts the accuracy of SNP microarray-based genotyping and copy number analyses , 2010, Molecular human reproduction.
[6] Jürgen Brockmöller,et al. Amelogenin-based sex identification as a strategy to control the identity of DNA samples in genetic association studies. , 2010, Pharmacogenomics.
[7] D. Hougaard,et al. High-throughput genotyping on archived dried blood spot samples. , 2009, Genetic testing and molecular biomarkers.
[8] F. Wagner,et al. Cost‐efficient sequence‐specific priming–polymerase chain reaction screening for blood donors with rare phenotypes , 2008, Transfusion.
[9] A. Mustapha,et al. Evaluation of four template preparation methods for polymerase chain reaction‐based detection of Salmonella in ground beef and chicken , 2002, Letters in applied microbiology.
[10] M. Kew,et al. Comparison of hepatitis B virus DNA extractions from serum by the QIAamp blood kit, GeneReleaser, and the phenol-chloroform method , 1996, Journal of clinical microbiology.
[11] E. Beutler,et al. Identification of the second common Jewish Gaucher disease mutation makes possible population-based screening for the heterozygous state. , 1991, Proceedings of the National Academy of Sciences of the United States of America.
[12] R. Desnick,et al. Niemann-Pick type B disease. Identification of a single codon deletion in the acid sphingomyelinase gene and genotype/phenotype correlations in type A and B patients. , 1991, The Journal of clinical investigation.
[13] C. Férec,et al. A 3′ splice site consensus sequence mutation in the cystic fibrosis gene , 1990, Human Genetics.
[14] R. Myerowitz,et al. The major defect in Ashkenazi Jews with Tay-Sachs disease is an insertion in the gene for the alpha-chain of beta-hexosaminidase. , 1988, The Journal of biological chemistry.
[15] K. Abd-Elsalam,et al. Rapid and efficient extraction of genomic DNA from differentphytopathogenic fungi using DNAzol reagent , 2004, Biotechnology Letters.
[16] C. Costigan,et al. The Major Defect in Ashkenazi Jews with Tay-Sachs Disease Is an Insertion in the Gene for the at-Chain of &Hexosaminidase* , 2001 .
[17] R. Kaul,et al. Canavan disease: mutations among Jewish and non-Jewish patients. , 1994, American journal of human genetics.