Self-priming arrest by modified random oligonucleotides facilitates the quality control of whole genome amplification
- 1 April 2005
- journal article
- Published by Elsevier in Analytical Biochemistry
- Vol. 339 (2) , 345-347
- https://doi.org/10.1016/j.ab.2005.01.005
Abstract
No abstract availableThis publication has 15 references indexed in Scilit:
- Chromosome paints from single copies of chromosomes.Chromosome Research, 2004
- Role of polymorphisms in MTHFR and MTHFD1 genes in the outcome of childhood acute lymphoblastic leukemiaThe Pharmacogenomics Journal, 2003
- Characterization of the BclI Polymorphism in the Glucocorticoid Receptor GeneClinical Chemistry, 2003
- Rubicon Genomics, Inc.Pharmacogenomics, 2002
- Comprehensive human genome amplification using multiple displacement amplificationProceedings of the National Academy of Sciences, 2002
- Rapid Amplification of Plasmid and Phage DNA Using Phi29 DNA Polymerase and Multiply-Primed Rolling Circle AmplificationGenome Research, 2001
- Mutation detection and single-molecule counting using isothermal rolling-circle amplificationNature Genetics, 1998
- ø29 DNA polymerase requires the N-terminal domain to bind terminal protein and DNA primer substratesJournal of Molecular Biology, 1998
- Preimplantation single-cell analysis of multiple genetic loci by whole-genome amplification.Proceedings of the National Academy of Sciences, 1994
- Whole genome amplification from a single cell: implications for genetic analysis.Proceedings of the National Academy of Sciences, 1992