Analysis of deletion breakpoints from 1,092 humans reveals details of mutation mechanisms (Q35672565)

9 August 2017

Analysis of deletion breakpoints from 1,092 humans reveals details of mutation mechanisms (English)

1 reference

PubMed ID

26028266

Erratum: Analysis of deletion breakpoints from 1,092 humans reveals details of mutation mechanisms

9 August 2017

corrigendum / erratum

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12 July 2019

http://api.crossref.org/works?select=update-to&filter=doi:10.1038/NCOMMS9389

author

Mark Bender Gerstein

14

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12 June 2020

Alexej Abyzov

1

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12 June 2020

Daniel Rhee Kim

3

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12 June 2020

Nicholas F Parrish

6

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12 June 2020

Jan Korbel

11

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12 June 2020

author name string

Shantao Li

2

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12 June 2020

Marghoob Mohiyuddin

4

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12 June 2020

Adrian M Stütz

5

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12 June 2020

Xinmeng Jasmine Mu

7

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12 June 2020

Wyatt Clark

8

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12 June 2020

Ken Chen

9

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12 June 2020

Matthew Hurles

10

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12 June 2020

Hugo Y K Lam

12

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12 June 2020

Charles Lee

13

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12 June 2020

language of work or name

English

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publication date

1 June 2015

1 reference

9 August 2017

Nature Communications

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12 June 2020

volume

6

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12 June 2020

page(s)

7256

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https://scigraph.springernature.com/pub.10.1038/ncomms8256

12 June 2020

exact match

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Genomic hypomethylation in the human germline associates with selective structural mutability in the human genome

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12 July 2018

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12 July 2018

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12 July 2018

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12 July 2018

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12 July 2018

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12 July 2018

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12 July 2018

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12 July 2018

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12 July 2018

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12 July 2018

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12 July 2018

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12 July 2018

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12 July 2018

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Deletion polymorphism upstream of IRGM associated with altered IRGM expression and Crohn's disease

12 July 2018

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A DNA replication mechanism for generating nonrecurrent rearrangements associated with genomic disorders

12 July 2018

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Germline rates of de novo meiotic deletions and duplications causing several genomic disorders

12 July 2018

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Strong association of de novo copy number mutations with autism

12 July 2018

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Structural variation of the human genome

12 July 2018

1 reference

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Genomic disorders: molecular mechanisms for rearrangements and conveyed phenotypes

12 July 2018

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Structural variation in the human genome

12 July 2018

1 reference

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Comparative recombination rates in the rat, mouse, and human genomes

12 July 2018

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Glocal alignment: finding rearrangements during alignment

12 July 2018

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12 July 2018

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Target DNA chromatinization modulates nicking by L1 endonuclease

12 July 2018

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Alu repeated DNAs are differentially methylated in primate germ cells

12 July 2018

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Restriction fragment length polymorphism caused by a deletion involving Alu sequences within the human alpha 2-plasmin inhibitor gene

12 July 2018

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Mechanisms of formation of structural variation in a fully sequenced human genome

12 July 2018

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Extensive genomic and transcriptional diversity identified through massively parallel DNA and RNA sequencing of eighteen Korean individuals.

25 September 2018

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HapMap methylation-associated SNPs, markers of germline DNA methylation, positively correlate with regional levels of human meiotic recombination

25 September 2018

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Alu retrotransposition-mediated deletion.

25 September 2018

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25 September 2018

Identifiers

DOI

10.1038/NCOMMS8256

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26028266%20AND%20SRC:MED&resulttype=core&format=json

12 June 2020

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Dimensions Publication ID

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1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26028266%20AND%20SRC:MED&resulttype=core&format=json

12 June 2020

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