Automated detection of point mutations using fluorescent sequence trace subtraction (Q39724486)

14 September 2017

Automated detection of point mutations using fluorescent sequence trace subtraction (English)

1 reference

14 September 2017

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Bonfield JK

1

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14 September 2017

Rada C

series ordinal

2

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14 September 2017

Staden R

series ordinal

3

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14 September 2017

language of work or name

English

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publication date

1 July 1998

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14 September 2017

Nucleic Acids Research

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14 September 2017

26

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14 September 2017

14

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14 September 2017

3404-3409

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

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=147706

Analysis of somatic hypermutation in mouse Peyer's patches using immunoglobulin kappa light-chain transgenes

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=147706

Molecular diagnosis of mucopolysaccharidosis type II (Hunter syndrome) by automated sequencing and computer-assisted interpretation: toward mutation mapping of the iduronate-2-sulfatase gene

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=147706

The application of numerical estimates of base calling accuracy to DNA sequencing projects

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=147706

Detection and localization of single base changes by denaturing gradient gel electrophoresis

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=147706

Reactivity of cytosine and thymine in single-base-pair mismatches with hydroxylamine and osmium tetroxide and its application to the study of mutations

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=147706

Detection of polymorphisms of human DNA by gel electrophoresis as single-strand conformation polymorphisms

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=147706

Hydrolink gels: a rapid and simple approach to the detection of DNA mutations in thromboembolic disease

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=147706

A standard file format for data from DNA sequencing instruments

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=147706

A new DNA sequence assembly program

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=147706

The rapid detection of unknown mutations in nucleic acids.

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=147706

Somatic hypermutation of immunoglobulin kappa may depend on sequences 3' of C kappa and occurs on passenger transgenes.

25 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=147706

Experiment files and their application during large-scale sequencing projects.

25 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=147706

Peak height variations in automated sequencing of PCR products using Taq dye-terminator chemistry

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=147706

The 5' hypermutation boundary of kappa chains is independent of local and neighbouring sequences and related to the distance from the initiation of transcription.

17 June 2018

1 reference

https://api.crossref.org/works/10.1093%2FNAR%2F26.14.3404

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

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=147706

[31] Detection and localization of single base changes by denaturing gradient gel electrophoresis

20 August 2018

1 reference

https://api.crossref.org/works/10.1093%2FNAR%2F26.14.3404

Comparative Analysis of Human DNA Variations by Fluorescence-Based Sequencing of PCR Products

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FNAR%2F26.14.3404

Detecting single base substitutions as heteroduplex polymorphisms

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FNAR%2F26.14.3404

Systematic use of automated fluorescence-based sequence analysis of amplified genomic DNA for rapid detection of point mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FNAR%2F26.14.3404

Nomenclature Committee of the International Union of Biochemistry (NC-IUB). Nomenclature for incompletely specified bases in nucleic acid sequences. Recommendations 1984

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FNAR%2F26.14.3404

21 January 2018

Identifiers

DOI

10.1093/NAR/26.14.3404

1 reference

14 September 2017

1 reference

14 September 2017

1 reference