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  A whole genome amplification method to generate long fragments from low quantities of genomic DNA

Kittler, R., Stoneking, M., & Kayser, M. (2002). A whole genome amplification method to generate long fragments from low quantities of genomic DNA. Analytical Biochemistry, 300(2), 237-244. doi:10.1006/abio.2001.5460.

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 Creators:
Kittler, Ralf1, Author           
Stoneking, Mark1, 2, Author           
Kayser, Manfred1, Author           
Affiliations:
1Department of Evolutionary Genetics, Max Planck Institute for Evolutionary Anthropology, Max Planck Society, ou_1497672              
2Human Population History, Department of Evolutionary Genetics, Max Planck Institute for Evolutionary Anthropology, Max Planck Society, Deutscher Platz 6, 04103 Leipzig, DE, ou_2074313              

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Free keywords: whole genome amplification; degenerate oligonucleotide-primed PCR; DOP-PCR; STR; short tandem repeats; microsatellites
 Abstract: Several whole genome amplification strategies have been developed to preamplify the entire genome from minimal amounts of DNA for subsequent molecular genetic analysis. However, none of these techniques has proven to amplify long products from very low (nanogram or picogram) quantities of genomic DNA. Here we report a new whole genome amplification protocol using a degenerate primer (DOP-PCR) that generates products up to about 10 kb in length from less than 1 ng genomic template DNA. This new protocol (LL-DOP-PCR) allows in the subsequent PCR the specific amplification, with high fidelity, of DNA fragments that are more than 1 kb in length. LL-DOP-PCR provides significantly better coverage for microsatellites and unique sequences in comparison to a conventional DOP-PCR method. (C) 2001 Elsevier Science.

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Language(s): eng - English
 Dates: 2002
 Publication Status: Issued
 Pages: -
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: eDoc: 21707
DOI: 10.1006/abio.2001.5460
ISI: 000173371000017
 Degree: -

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Title: Analytical Biochemistry
  Alternative Title : Anal. Biochem.
Source Genre: Journal
 Creator(s):
Affiliations:
Publ. Info: -
Pages: - Volume / Issue: 300 (2) Sequence Number: - Start / End Page: 237 - 244 Identifier: ISSN: 0003-2697