dbDNV: a resource of duplicated gene nucleotide variants in human genome (Q24610538)

1

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Kuo-Wang Tsai

2

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Chun-houh Chen

3

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Wen-chang Lin

Creative Commons Attribution-NonCommercial 2.5 Generic

4

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language of work or name

English

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publication date

January 2011

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published in

Nucleic Acids Research

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volume

39

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issue

Database issue

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page(s)

D920-5

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copyright license

start time

14 November 2016

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

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cites work

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7 April 2017

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7 April 2017

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Large-scale inference of the point mutational spectrum in human segmental duplications

27 September 2017

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Quantitative analysis of single nucleotide polymorphisms within copy number variation

27 September 2017

1 reference

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Gene dosage and gene duplicability

27 September 2017

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Gene duplication in early vertebrates results in tissue-specific subfunctionalized adaptor proteins: CASP and GRASP.

27 September 2017

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Identification and analysis of genes and pseudogenes within duplicated regions in the human and mouse genomes

27 September 2017

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Diagnosing duplications--can it be done?

27 September 2017

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Detection of gene duplications and block duplications in eukaryotic genomes

27 September 2017

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RNAs from all categories generate retrosequences that may be exapted as novel genes or regulatory elements

27 September 2017

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Gene family evolution by duplication, speciation, and loss

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SNPs in genes with copy number variation: a question of specificity.

28 November 2018

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Role of duplicate genes in robustness against deleterious human mutations

28 November 2018

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28 November 2018

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Complex patterns of copy number variation at sites of segmental duplications: an important category of structural variation in the human genome.

28 November 2018

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28 November 2018

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28 November 2018

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Genetics. More than just a copy

28 November 2018

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PubMed

https://pubmed.ncbi.nlm.nih.gov/21097891

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Chromosomal regions containing high-density and ambiguously mapped putative single nucleotide polymorphisms (SNPs) correlate with segmental duplications in the human genome

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21097891

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Shotgun sequence assembly and recent segmental duplications within the human genome

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21097891

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1093/NAR/GKQ1197

1 reference

1 reference

DBLP Dataset 2021-01-02

28 January 2021

4581425

1 reference

1 reference

1 reference