Jump to content

PolyPhred: automating the detection and genotyping of single nucleotide substitutions using fluorescence-based resequencing (Q29618564)

From Wikidata

scientific article (publication date: 15 July 1997)

Language	Label	Description	Also known as
default for all languages	No label defined
English	PolyPhred: automating the detection and genotyping of single nucleotide substitutions using fluorescence-based resequencing	scientific article (publication date: 15 July 1997)

Statements

scholarly article

0 references

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=9207020

30 April 2017

0 references

author name string

Nickerson DA

1

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=9207020

30 April 2017

Tobe VO

2

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=9207020

30 April 2017

Taylor SL

3

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=9207020

30 April 2017

publication date

15 July 1997

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=9207020

30 April 2017

language of work or name

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=9207020

30 April 2017

Nucleic Acids Research

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=9207020

30 April 2017

25

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=9207020

30 April 2017

14

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=9207020

30 April 2017

2745-51

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=9207020

30 April 2017

Mutations in the kinase Rsk-2 associated with Coffin-Lowry syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=146817

30 April 2017

Association between X-linked mixed deafness and mutations in the POU domain gene POU3F4

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=146817

30 April 2017

Rapid and sensitive detection of point mutations and DNA polymorphisms using the polymerase chain reaction

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=146817

30 April 2017

Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=146817

30 April 2017

Detection of heterozygous mutations in BRCA1 using high density oligonucleotide arrays and two-colour fluorescence analysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=146817

3 June 2018

AmpliTaq DNA polymerase, FS dye-terminator sequencing: analysis of peak height patterns

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=146817

3 June 2018

Single-well genotyping of diallelic sequence variations by a two-color ELISA-based oligonucleotide ligation assay

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=146817

3 June 2018

Applications of heteroduplex analysis for mutation detection in disease genes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=146817

3 June 2018

The rapid detection of unknown mutations in nucleic acids.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=146817

3 June 2018

High-resolution HLA-DPB typing based upon computerized analysis of data obtained by fluorescent sequencing of the amplified polymorphic exon 2.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=146817

3 June 2018

Mitochondrial DNA sequence variation in human evolution and disease.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=146817

3 June 2018

Sequence-based analysis of the human p53 gene based on microdissection of tumor biopsy samples.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=146817

3 June 2018

Screening for mutations by enzyme mismatch cleavage with T4 endonuclease VII.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=146817

3 June 2018

Fluorescence energy transfer dye-labeled primers for DNA sequencing and analysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=146817

3 June 2018

Detection of single base substitutions by ribonuclease cleavage at mismatches in RNA:DNA duplexes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=146817

3 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=146817

3 June 2018

Identification of mutations leading to the Lesch-Nyhan syndrome by automated direct DNA sequencing of in vitro amplified cDNA.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=146817

3 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=146817

3 June 2018

HLA class II "typing": direct sequencing of DRB, DQB, and DQA genes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=146817

3 June 2018

Identification of clusters of biallelic polymorphic sequence-tagged sites (pSTSs) that generate highly informative and automatable markers for genetic linkage mapping

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=146817

3 June 2018

Accessing genetic information with high-density DNA arrays

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=146817

26 November 2018

Increasing the information content of STS-based genome maps: identifying polymorphisms in mapped STSs

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=146817

26 November 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=146817

26 November 2018

Identifying DNA polymorphisms in human TCRA/D variable genes by direct sequencing of PCR products

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=146817

26 November 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=146817

26 November 2018

An estimate of unique DNA sequence heterozygosity in the human genome

1 reference

https://pubmed.ncbi.nlm.nih.gov/9207020

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

HLA sequence polymorphism and the origin of humans

1 reference

https://pubmed.ncbi.nlm.nih.gov/9207020

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Orphan peak analysis: a novel method for detection of point mutations using an automated fluorescence DNA sequencer

1 reference

https://pubmed.ncbi.nlm.nih.gov/9207020

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Screening for point mutations by semi-automated DNA sequencing using sequenase and magnetic beads

1 reference

https://pubmed.ncbi.nlm.nih.gov/9207020

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A collaborative survey of 80 mutations in the BRCA1 breast and ovarian cancer susceptibility gene. Implications for presymptomatic testing and screening

1 reference

https://pubmed.ncbi.nlm.nih.gov/9207020

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Validation of mitochondrial DNA sequencing for forensic casework analysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/9207020

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Electrophoretically uniform fluorescent dyes for automated DNA sequencing

1 reference

https://pubmed.ncbi.nlm.nih.gov/9207020

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1093/NAR/25.14.2745

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

PMC publication ID

2 references

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=9207020

30 April 2017

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

PubMed publication ID

2 references

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=9207020

30 April 2017

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

ResearchGate publication ID

0 references

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q29618564&oldid=1389538907"