An isothermal primer extension method for whole genome amplification of fresh and degraded DNA: Applications in comparative genomic hybridization, genotyping and mutation screening

Nature Protocols

Volumn 1, Issue 5, 2006, Pages 2185-2194

  Lee, Cheryl I P ^a   Leong, Siew Hong ^a   Png, Adrian E H ^b   Choo, Keng Wah ^b   Syn, Christopher ^c   Lim, Dennis T H ^d   Law, Hai Yang ^e   Kon, Oi Lian ^a  

^a DIVISION OF MEDICAL ONCOLOGY   (Singapore)

^b SCHOOL OF ENGINEERING   (Singapore)

^c HEALTH SCIENCES AUTHORITY   (Singapore)

^d SINGAPORE GENERAL HOSPITAL   (Singapore)

^e KK WOMEN'S AND CHILDREN'S HOSPITAL   (Singapore)

Author keywords

[No Author keywords available]

Indexed keywords

DIAGNOSTIC AGENT; DNA; PRIMER DNA;

ARTICLE; BACTERIAL ARTIFICIAL CHROMOSOME; BETA THALASSEMIA; DNA MICROARRAY; GENETICS; GENOME; GENOTYPE; HUMAN; METHODOLOGY; NUCLEIC ACID AMPLIFICATION; NUCLEIC ACID HYBRIDIZATION; POINT MUTATION; TANDEM REPEAT; TEMPERATURE;

BETA-THALASSEMIA; CHROMOSOMES, ARTIFICIAL, BACTERIAL; DNA; DNA PRIMERS; GENOME, HUMAN; GENOTYPE; HUMANS; NUCLEIC ACID AMPLIFICATION TECHNIQUES; NUCLEIC ACID HYBRIDIZATION; OLIGONUCLEOTIDE ARRAY SEQUENCE ANALYSIS; POINT MUTATION; TANDEM REPEAT SEQUENCES; TEMPERATURE;

EID: 34548862304     PISSN: 17542189     EISSN: 17502799     Source Type: Journal    
DOI: 10.1038/nprot.2006.398     Document Type: Article

References (10)

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