(Q33312214)

25 July 2017

Closing gaps in the human genome with fosmid resources generated from multiple individuals (English)

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25 July 2017

3

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25 July 2017

7

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25 July 2017

20

Evan E Eichler

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25 July 2017

9

Nick Sampas

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25 July 2017

10

Karen Phelps

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25 July 2017

Donald Bovee

1

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25 July 2017

Yang Zhou

2

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25 July 2017

Zaining Wu

4

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25 July 2017

Hillary S Hayden

5

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25 July 2017

Will Gillett

6

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25 July 2017

Gregory M Cooper

8

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25 July 2017

Ruth Levy

11

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25 July 2017

V Anne Morrison

12

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25 July 2017

James Sprague

13

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25 July 2017

Donald Jewett

14

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25 July 2017

Danielle Buckley

15

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25 July 2017

Sandhya Subramaniam

16

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25 July 2017

Jean Chang

17

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25 July 2017

Douglas R Smith

18

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25 July 2017

Maynard V Olson

19

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25 July 2017

Rajinder Kaul

21

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25 July 2017

language of work or name

English

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publication date

23 December 2007

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25 July 2017

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25 July 2017

40

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25 July 2017

96-101

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25 July 2017

1

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https://scigraph.springernature.com/pub.10.1038/ng.2007.34

25 July 2017

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cites work

Finishing the euchromatic sequence of the human genome

1 reference

https://api.crossref.org/works/10.1038%2FNG.2007.34

7 January 2021

An assessment of the sequence gaps: unfinished business in a finished human genome

1 reference

https://api.crossref.org/works/10.1038%2FNG.2007.34

7 January 2021

Recent segmental duplications in the human genome

1 reference

https://api.crossref.org/works/10.1038%2FNG.2007.34

7 January 2021

Whole-genome shotgun assembly and comparison of human genome assemblies

1 reference

https://api.crossref.org/works/10.1038%2FNG.2007.34

7 January 2021

Large-scale copy number polymorphism in the human genome

1 reference

https://api.crossref.org/works/10.1038%2FNG.2007.34

7 January 2021

Detection of large-scale variation in the human genome

1 reference

https://api.crossref.org/works/10.1038%2FNG.2007.34

7 January 2021

Fine-scale structural variation of the human genome

1 reference

https://api.crossref.org/works/10.1038%2FNG.2007.34

7 January 2021

Segmental duplications and copy-number variation in the human genome

1 reference

https://api.crossref.org/works/10.1038%2FNG.2007.34

7 January 2021

Widening the spectrum of human genetic variation

1 reference

https://api.crossref.org/works/10.1038%2FNG.2007.34

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG.2007.34

7 January 2021

Copy number variation: new insights in genome diversity

1 reference

https://api.crossref.org/works/10.1038%2FNG.2007.34

7 January 2021

Common deletions and SNPs are in linkage disequilibrium in the human genome

1 reference

https://api.crossref.org/works/10.1038%2FNG.2007.34

7 January 2021

Genome assembly comparison identifies structural variants in the human genome.

1 reference

https://api.crossref.org/works/10.1038%2FNG.2007.34

7 January 2021

Common deletion polymorphisms in the human genome.

1 reference

https://api.crossref.org/works/10.1038%2FNG.2007.34

7 January 2021

Global variation in copy number in the human genome

1 reference

https://api.crossref.org/works/10.1038%2FNG.2007.34

7 January 2021

Structural variation in the human genome

1 reference

https://api.crossref.org/works/10.1038%2FNG.2007.34

7 January 2021

Copy number polymorphism in Fcgr3 predisposes to glomerulonephritis in rats and humans

1 reference

https://api.crossref.org/works/10.1038%2FNG.2007.34

7 January 2021

The influence of CCL3L1 gene-containing segmental duplications on HIV-1/AIDS susceptibility

1 reference

https://api.crossref.org/works/10.1038%2FNG.2007.34

7 January 2021

A common inversion under selection in Europeans

1 reference

https://api.crossref.org/works/10.1038%2FNG.2007.34

7 January 2021

A chromosome 8 gene-cluster polymorphism with low human beta-defensin 2 gene copy number predisposes to Crohn disease of the colon

1 reference

https://api.crossref.org/works/10.1038%2FNG.2007.34

7 January 2021

Chemical characterization of element 112

1 reference

https://api.crossref.org/works/10.1038%2FNG.2007.34

7 January 2021

Multiple-complete-digest restriction fragment mapping: generating sequence-ready maps for large-scale DNA sequencing

1 reference

https://api.crossref.org/works/10.1038%2FNG.2007.34

7 January 2021

High-throughput genotyping of intermediate-size structural variation

1 reference

https://api.crossref.org/works/10.1038%2FNG.2007.34

7 January 2021

A preliminary comparative analysis of primate segmental duplications shows elevated substitution rates and a great-ape expansion of intrachromosomal duplications

1 reference

https://api.crossref.org/works/10.1038%2FNG.2007.34

7 January 2021

Segments missing from the draft human genome sequence can be isolated by transformation-associated recombination cloning in yeast

1 reference

https://api.crossref.org/works/10.1038%2FNG.2007.34

7 January 2021

Closing the gaps on human chromosome 19 revealed genes with a high density of repetitive tandemly arrayed elements

1 reference

https://api.crossref.org/works/10.1038%2FNG.2007.34

7 January 2021

Targeted, haplotype-resolved resequencing of long segments of the human genome

1 reference

https://api.crossref.org/works/10.1038%2FNG.2007.34

7 January 2021

Identifiers

DOI

10.1038/NG.2007.34

1 reference

Dimensions Publication ID

25 July 2017

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