(Q48047736)

8 February 2018

title

CNVD: text mining-based copy number variation in disease database (English)

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8 February 2018

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Fujun Qiu

1

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8 February 2018

Yan Xu

2

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8 February 2018

Kening Li

3

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8 February 2018

Zihui Li

4

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8 February 2018

Yufeng Liu

5

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8 February 2018

Huizi DuanMu

6

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8 February 2018

Shanzhen Zhang

7

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8 February 2018

Zhenqi Li

8

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8 February 2018

Zhiqiang Chang

9

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8 February 2018

Yuanshuai Zhou

10

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8 February 2018

Rui Zhang

11

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8 February 2018

Shujuan Zhang

12

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8 February 2018

Chunquan Li

13

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8 February 2018

Yan Zhang

14

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8 February 2018

Minzhai Liu

15

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8 February 2018

Xia Li

16

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8 February 2018

publication date

23 July 2012

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8 February 2018

published in

Human Mutation

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8 February 2018

volume

33

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8 February 2018

issue

11

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8 February 2018

page(s)

E2375-81

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8 February 2018

Gene ontology: tool for the unification of biology

cites work

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22163

The landscape of somatic copy-number alteration across human cancers

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22163

CaSNP: a database for interrogating copy number alterations of cancer genome from SNP array data

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22163

CNVVdb: a database of copy number variations across vertebrate genomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22163

Analysis of LKB1 mutations and other molecular alterations in pancreatic acinar cell carcinoma.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22163

Copy number variation: new insights in genome diversity

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22163

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22163

The Ensembl genome database project

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22163

Detection of large-scale variation in the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22163

Nuclear topography of the 1q21 genomic region and Mcl-1 protein levels associated with pathophysiology of multiple myeloma.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22163

Human defensin gene copy number polymorphisms: comprehensive analysis of independent variation in alpha- and beta-defensin regions at 8p22-p23.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22163

Global variation in copy number in the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22163

Structural variation in the human genome: the impact of copy number variants on clinical diagnosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22163

Structural variation in the human genome and its role in disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22163

Genomic copy number variation, human health, and disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22163

Development of bioinformatics resources for display and analysis of copy number and other structural variants in the human genome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22163

An integrated view of copy number and allelic alterations in the cancer genome using single nucleotide polymorphism arrays

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22163

21 January 2018

Identifiers

DOI

10.1002/HUMU.22163

1 reference

8 February 2018

release_6dhmg7j3unau3f4z7sum4lurum

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/6dhmg7j3unau3f4z7sum4lurum

mapped directly with Wikidata item

24 November 2022

based on heuristic

1 reference

8 February 2018