Literature DB >> 10407782

Automated mutation analysis.

D Ravine1.   

Abstract

Automated mutation analysis brings with it a vastly increased capacity in the number of test samples that can be processed at a time, as well as much improved test reproducibility. Until now, the introduction of automation into this field had been restricted to the use of semiautomated sequencing systems to make the most of the sequence information extractable from a single lane in an electrophoretic gel or in a polymer-filled glass capillary. Much effort is now being directed into harnessing the potential of DNA microarrays (DNA chips) and there is increasing interest in the potential of matrix-assisted mass spectrometry for determining the detail of large nucleic acid molecules. Meanwhile, there are other important recent developments already available, including robotic workstations, the further development of the allele-specific oligonucleotide assay into microtitre formats, and its use with fluorescence for real-time quantitative PCR analysis. Implementation of these developments in appropriate settings can further streamline the routine of molecular diagnostic laboratories, allowing them to take greater advantage of the recent surge of gene discoveries and their associated disease-causing mutations.

Entities:  

Mesh:

Year:  1999        PMID: 10407782     DOI: 10.1023/a:1005508324048

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN: 0141-8955            Impact factor:   4.982


  93 in total

1.  Critical factors in the performance and cost of two-dimensional gene scanning: RB1 as a model.

Authors:  R K Dhanda; N J van Orsouw; I Sigalas; C Eng; J Vijg
Journal:  Biotechniques       Date:  1998-10       Impact factor: 1.993

2.  Mutation detection with MutH, MutL, and MutS mismatch repair proteins.

Authors:  J Smith; P Modrich
Journal:  Proc Natl Acad Sci U S A       Date:  1996-04-30       Impact factor: 11.205

3.  DNA sequencing by delayed extraction-matrix-assisted laser desorption/ionization time of flight mass spectrometry.

Authors:  M T Roskey; P Juhasz; I P Smirnov; E J Takach; S A Martin; L A Haff
Journal:  Proc Natl Acad Sci U S A       Date:  1996-05-14       Impact factor: 11.205

4.  Primer extension technique for the detection of single nucleotide in genomic DNA.

Authors:  B P Sokolov
Journal:  Nucleic Acids Res       Date:  1990-06-25       Impact factor: 16.971

5.  PCR-based screening for cystic fibrosis carrier mutations in an ethnically diverse pregnant population.

Authors:  W W Grody; C Dunkel-Schetter; Z H Tatsugawa; M A Fox; C Y Fang; R M Cantor; J M Novak; H N Bass; B F Crandall
Journal:  Am J Hum Genet       Date:  1997-04       Impact factor: 11.025

Review 6.  Trinucleotide repeats associated with human disease.

Authors:  M Mitas
Journal:  Nucleic Acids Res       Date:  1997-06-15       Impact factor: 16.971

7.  A model for high-throughput automated DNA sequencing and analysis core facilities.

Authors:  M D Adams; A R Kerlavage; J M Kelley; J D Gocayne; C Fields; C M Fraser; J C Venter
Journal:  Nature       Date:  1994-03-31       Impact factor: 49.962

8.  Diagnosis of a deletion of steroid sulfatase by polymerase chain reaction and high-performance liquid chromatography.

Authors:  T Sugawara; M Iwaki; S Fujimoto
Journal:  Clin Chim Acta       Date:  1997-07-04       Impact factor: 3.786

9.  Accurate diagnosis of carriers of deletions and duplications in Duchenne/Becker muscular dystrophy by fluorescent dosage analysis.

Authors:  S C Yau; M Bobrow; C G Mathew; S J Abbs
Journal:  J Med Genet       Date:  1996-07       Impact factor: 6.318

10.  Oligonucleotide ligation assay (OLA) for the diagnosis of familial hypercholesterolemia.

Authors:  H Baron; S Fung; A Aydin; S Bähring; F C Luft; H Schuster
Journal:  Nat Biotechnol       Date:  1996-10       Impact factor: 54.908

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  1 in total

1.  Diagnostic uses of DNA analysis: powerful but problematic.

Authors: 
Journal:  J Inherit Metab Dis       Date:  1999-08       Impact factor: 4.982

  1 in total

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