Literature DB >> 8747666

Efficient, automatic detection of heterozygous bases during large-scale DNA sequence screening.

R S Phelps1, R B Chadwick, M P Conrad, M N Kronick, A Kamb.   

Abstract

A crucial factor in the success of positional cloning efforts is the ability to screen rapidly many different candidate genes for mutations. By modifying standard software, we have improved the detection of heterozygous base positions in PCR products sequenced by cycle sequencing. A key element of the method is the incorporation of a modified heterozygote detection algorithm that permits the use of DNA sequence data derived from PCR and sequencing reactions that have not been fully optimized. This allows sequencing runs of average quality to be used. We demonstrate that the sensitivity and specificity of the method are well suited to mutation detection applications such as positional cloning.

Mesh:

Year:  1995        PMID: 8747666

Source DB:  PubMed          Journal:  Biotechniques        ISSN: 0736-6205            Impact factor:   1.993


  7 in total

1.  Automated detection of point mutations using fluorescent sequence trace subtraction.

Authors:  J K Bonfield; C Rada; R Staden
Journal:  Nucleic Acids Res       Date:  1998-07-15       Impact factor: 16.971

2.  Automating the identification of DNA variations using quality-based fluorescence re-sequencing: analysis of the human mitochondrial genome.

Authors:  M J Rieder; S L Taylor; V O Tobe; D A Nickerson
Journal:  Nucleic Acids Res       Date:  1998-02-15       Impact factor: 16.971

3.  Detection of unknown mutations in DNA: a catch-22.

Authors:  R G Cotton
Journal:  Am J Hum Genet       Date:  1996-08       Impact factor: 11.025

4.  Exhaustive mutation scanning by fluorescence-assisted mismatch analysis discloses new genotype-phenotype correlations in angiodema.

Authors:  E Verpy; M Biasotto; M Brai; G Misiano; T Meo; M Tosi
Journal:  Am J Hum Genet       Date:  1996-08       Impact factor: 11.025

5.  PolyPhred: automating the detection and genotyping of single nucleotide substitutions using fluorescence-based resequencing.

Authors:  D A Nickerson; V O Tobe; S L Taylor
Journal:  Nucleic Acids Res       Date:  1997-07-15       Impact factor: 16.971

6.  Detection of all single-base mismatches in solution by chemiluminescence.

Authors:  N C Nelson; P W Hammond; E Matsuda; A A Goud; M M Becker
Journal:  Nucleic Acids Res       Date:  1996-12-15       Impact factor: 16.971

7.  Exhaustive screening of the acid beta-glucosidase gene, by fluorescence-assisted mismatch analysis using universal primers: mutation profile and genotype/phenotype correlations in Gaucher disease.

Authors:  D P Germain; J P Puech; C Caillaud; A Kahn; L Poenaru
Journal:  Am J Hum Genet       Date:  1998-08       Impact factor: 11.025

  7 in total

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