Literature DB >> 21030955

MeltMADGE for mutation scanning of specific genes in population studies.

Khalid K Alharbi1, Mohammed A Aldahmesh, Tom R Gaunt, Hamid Rassoulian, Philip Ai Guthrie, Santiago Rodriguez, Christopher R Boustred, Emmanuel Spanakis, Ian N M Day.   

Abstract

MeltMADGE reconfigures the mutation scanning process of denaturing gradient gel electrophoresis so that the independent variable is time rather than space and the dependent (denaturing) variable is temperature rather than concentration of chemical denaturant. Use of a thermal ramp enables the use of a homogeneous gel and therefore of high-density arrays of wells such as those of microplate array diagonal gel electrophoresis (MADGE). In this configuration, electrophoresis of products on 10-12 96-well meltMADGE gels can be conducted in a 1- to 2-liter tank in a 1- to 2-h run, enabling the scanning of a target amplicon in over 1,000 subjects simultaneously. Gels are read by imaging the fluorescence of UV-excited ethidium bromide, giving a simple, economical system for identifying rarer sequence variants in target genes; it is suitable for large-scale case-control or population studies and other comparable applications. Different amplicons with similar melting characteristics can also be combined in the same run.

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Year:  2010        PMID: 21030955      PMCID: PMC3575632          DOI: 10.1038/nprot.2010.136

Source DB:  PubMed          Journal:  Nat Protoc        ISSN: 1750-2799            Impact factor:   13.491


  31 in total

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Authors:  S D O'Dell; X Chen; I N Day
Journal:  Hum Mutat       Date:  2000       Impact factor: 4.878

2.  Manual 768 or 384 well microplate gel 'dry' electrophoresis for PCR checking and SNP genotyping.

Authors:  Tom R Gaunt; Lesley J Hinks; Hamid Rassoulian; Ian N M Day
Journal:  Nucleic Acids Res       Date:  2003-05-01       Impact factor: 16.971

3.  Molecular structure of nucleic acids; a structure for deoxyribose nucleic acid.

Authors:  J D WATSON; F H CRICK
Journal:  Nature       Date:  1953-04-25       Impact factor: 49.962

4.  Attachment of a 40-base-pair G + C-rich sequence (GC-clamp) to genomic DNA fragments by the polymerase chain reaction results in improved detection of single-base changes.

Authors:  V C Sheffield; D R Cox; L S Lerman; R M Myers
Journal:  Proc Natl Acad Sci U S A       Date:  1989-01       Impact factor: 11.205

5.  Analysis of mutations using PCR and denaturing gradient gel electrophoresis.

Authors:  N F Cariello; J A Swenberg; A De Bellis; T R Skopek
Journal:  Environ Mol Mutagen       Date:  1991       Impact factor: 3.216

Review 6.  High-resolution DNA melting analysis: advancements and limitations.

Authors:  Carl T Wittwer
Journal:  Hum Mutat       Date:  2009-06       Impact factor: 4.878

7.  Detection of numerous Y chromosome biallelic polymorphisms by denaturing high-performance liquid chromatography.

Authors:  P A Underhill; L Jin; A A Lin; S Q Mehdi; T Jenkins; D Vollrath; R W Davis; L L Cavalli-Sforza; P J Oefner
Journal:  Genome Res       Date:  1997-10       Impact factor: 9.043

8.  Recursion relation generation of probability profiles for specific-sequence macromolecules with long-range correlations.

Authors:  D Poland
Journal:  Biopolymers       Date:  1974       Impact factor: 2.505

9.  Thermal denaturation of double-stranded nucleic acids: prediction of temperatures critical for gradient gel electrophoresis and polymerase chain reaction.

Authors:  G Steger
Journal:  Nucleic Acids Res       Date:  1994-07-25       Impact factor: 16.971

10.  Targeted capture and massively parallel sequencing of 12 human exomes.

Authors:  Sarah B Ng; Emily H Turner; Peggy D Robertson; Steven D Flygare; Abigail W Bigham; Choli Lee; Tristan Shaffer; Michelle Wong; Arindam Bhattacharjee; Evan E Eichler; Michael Bamshad; Deborah A Nickerson; Jay Shendure
Journal:  Nature       Date:  2009-08-16       Impact factor: 49.962

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