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  1. ...: A Practical Approach . Oxford University Press, Oxford, UK. ↵ Dean, F.B., Nelson, J.R., Giesler, T.L., and Lasken, R.S. 2001 . Rapid amplification of plasmid and phage DNA using Phi 29 DNA polymerase and multiply-primed rolling circle amplification. Genome Res. 11 : 1095 -1099. ↵ Dean, F.B., Hosono, S., Fang...
  2. ...). Abbreviations are as follows: aa-dUTP indicates 5-(3-aminoallyl)-29-deoxyuridine-59-triphosphate; dNTP, deoxyribonucleotide triphosphate; DpnI, restriction endonuclease from Diplococcus pneumoniae; EDTA, ethylenediaminetetraacetic acid;u29 polymerase, DNA polymerase from a Bacillus subtilis phage Phi29; M, 1 kb...
  3. ....J. , Bottomley W. , et al. ( 2002 ) Mutations of the BRAF gene in human cancer. Nature 417 : 949 – 954 . ↵ Dean F.B. , Nelson J.R. , Giesler T.L. , Lasken R.S. ( 2001 ) Rapid amplification of plasmid and phage DNA using φ29 DNA polymerase and multiply-primed rolling circle amplification. Genome Res. 11 : 1095...
  4. ...oligonucleotide primer allows hundreds of genotypes to be performed on less than one nanogram of genomic DNA. Proc. Natl. Acad. Sci. 93 : 14676 -14679. ↵ Dean, F.B., Nelson, J.R., Giesler, T.L., and Lasken, R.S. 2001 . Rapid amplification of plasmid and phage DNA using Phi 29 DNA polymerase and multiply-primed...
  5. .... This is largely due to our inability to culture most microorganisms in isolation, which is a prerequisite for traditional genome sequencing. Single-cell sequencing has allowed researchers to circumvent this limitation. DNA is amplified directly from a single cell using the whole-genome amplification technique...
  6. ...in parallel with each sort of single cells to determine the relative amount and identity of contaminating bacterial DNA in the MDA reagents; this is a necessary standard practice in single-cell genomics due to the highly processive strand displacement activity of the phi29 DNA polymerase and the near...
  7. ...Ridgway and Taylor-Robinson 1991). This implies that the growth of strains itself may impose a selective bias on the strains whose s we are able to sequence. It is clear that a rapid, simple, culture-independent technique for generating DNA for whole- sequencing is required. Whole- amplification (WGA...
  8. ...,Whittaker P, DelgadoM, et al. 2006. A high-resolution HLA and SNP haplotype map for disease association studies in the extended human MHC. Nat Genet 38: 1166–1172. Dean FB, Nelson JR, Giesler TL, Lasken RS. 2001. Rapid amplification of plasmid and phage DNA using phi29 DNA polymerase and multiplyprimed...
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