Short tandem repeats in human exons: a target for disease mutations (Q33369207)

26 July 2017

title

Short tandem repeats in human exons: a target for disease mutations (English)

1 reference

26 July 2017

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2

Palle Villesen

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26 July 2017

Carsten Wiuf

3

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author name string

Bo Eskerod Madsen

series ordinal

1

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26 July 2017

language of work or name

English

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publication date

12 September 2008

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26 July 2017

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26 July 2017

volume

9

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26 July 2017

page(s)

410

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Genome-wide in situ exon capture for selective resequencing

26 July 2017

cites work

1 reference

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Replication slippage versus point mutation rates in short tandem repeats of the human genome

28 July 2018

1 reference

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The diploid genome sequence of an individual human

28 July 2018

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A periodic pattern of SNPs in the human genome

28 July 2018

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28 July 2018

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Global variation in copy number in the human genome

28 July 2018

1 reference

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Genome assembly comparison identifies structural variants in the human genome.

28 July 2018

1 reference

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Copy number variation: new insights in genome diversity

28 July 2018

1 reference

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Simple sequence repeats as advantageous mutators in evolution

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2543027

Tandem repeat copy-number variation in protein-coding regions of human genes

28 July 2018

1 reference

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BioMart and Bioconductor: a powerful link between biological databases and microarray data analysis

28 July 2018

1 reference

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Comparative analysis of amino acid repeats in rodents and humans

28 July 2018

1 reference

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The UCSC Table Browser data retrieval tool

28 July 2018

1 reference

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The Mouse Genome Database (MGD): integrating biology with the genome.

28 July 2018

1 reference

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Initial sequencing and comparative analysis of the mouse genome

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2543027

Tandem repeats in protein coding regions of primate genes

28 July 2018

1 reference

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Initial sequencing and analysis of the human genome

28 July 2018

1 reference

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28 July 2018

1 reference

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Tandem repeats finder: a program to analyze DNA sequences

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2543027

Slipped-strand mispairing: a major mechanism for DNA sequence evolution

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2543027

The genome-wide determinants of human and chimpanzee microsatellite evolution

28 July 2018

1 reference

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Expandable DNA repeats and human disease.

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2543027

Detecting microsatellites within genomes: significant variation among algorithms

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2543027

Genome structural variation and sporadic disease traits

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2543027

Fine-scale structural variation of the human genome

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2543027

Simple sequence repeats in proteins and their significance for network evolution

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2543027

Online Mendelian Inheritance in Man (OMIM), a knowledgebase of human genes and genetic disorders

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2543027

TRbase: a database relating tandem repeats to disease genes for the human genome.

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2543027

The relationship between microsatellite slippage mutation rate and the number of repeat units

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2543027

A high-resolution survey of deletion polymorphism in the human genome

31 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18789129

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Genomics. DNA duplications and deletions help determine health

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18789129

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1186/1471-2164-9-410

1 reference

Dimensions Publication ID

26 July 2017

1 reference

https://scigraph.springernature.com/pub.10.1186/1471-2164-9-410

9 September 2019

1 reference

26 July 2017

1 reference