Whole genome amplification of single cells: mathematical analysis of PEP and tagged PCR
Author(s) -
Fengzhu Sun,
Norman Arnheim,
Michael S. Waterman
Publication year - 1995
Publication title -
nucleic acids research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 9.008
H-Index - 537
eISSN - 1362-4954
pISSN - 0305-1048
DOI - 10.1093/nar/23.15.3034
Subject(s) - biology , processivity , primer (cosmetics) , genome , polymerase chain reaction , genetics , microbiology and biotechnology , computational biology , polymerase , dna , gene , physics , thermodynamics
We construct a mathematical model for two whole genome amplification strategies, primer extension preamplification (PEP) and tagged polymerase chain reaction (tagged PCR). An explicit formula for the expected target yield of PEP is obtained. The distribution of the target yield and the coverage properties of these two strategies are studied by simulations. From our studies we find that polymerase with high processivity may increase the efficiency of PEP and tagged PCR.
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