๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

A Whole Genome Amplification Method to Generate Long Fragments from Low Quantities of Genomic DNA

โœ Scribed by Ralf Kittler; Mark Stoneking; Manfred Kayser


Publisher
Elsevier Science
Year
2002
Tongue
English
Weight
141 KB
Volume
300
Category
Article
ISSN
0003-2697

No coin nor oath required. For personal study only.

โœฆ Synopsis


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.


๐Ÿ“œ SIMILAR VOLUMES


A Method for Extraction of High-Quality
โœ Awdhesh Kalia; Ashok Rattan; Prem Chopra ๐Ÿ“‚ Article ๐Ÿ“… 1999 ๐Ÿ› Elsevier Science ๐ŸŒ English โš– 143 KB

In this study, we report a modified procedure for extraction of high-quality genomic DNA that is rapid, simple, biologically nonhazardous, and generally applicable to pathogenic bacteria. Bacterial cells were pretreated with 70% ethanol prior to enzymatic digestion with lysozyme. Exposure of bacteri

Clarification to: Evaluation of a whole-
๐Ÿ“‚ Article ๐Ÿ“… 2003 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 41 KB

## Abstract The original article to which this Clarification refers was published in Genes, Chromosomes, and Cancer (2003) 38(2) 168โ€“176