(Q41190098)

English

Characterization of 26 deletion CNVs reveals the frequent occurrence of micro-mutations within the breakpoint-flanking regions and frequent repair of double-strand breaks by templated insertions derived from remote genomic regions

scientific article published on 20 March 2015

In more languages

default for all languages

No label defined

No description defined

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

28 September 2017

Characterization of 26 deletion CNVs reveals the frequent occurrence of micro-mutations within the breakpoint-flanking regions and frequent repair of double-strand breaks by templated insertions derived from remote genomic regions (English)

1 reference

Europe PubMed Central

PubMed publication ID

28 September 2017

David N. Cooper

14

1 reference

Europe PubMed Central

PubMed publication ID

28 September 2017

object named as

Jiangchao Li

7

0 references

object named as

Jun Wang

15

0 references

author name string

Ye Wang

1

1 reference

Europe PubMed Central

PubMed publication ID

28 September 2017

Peiqiang Su

2

1 reference

Europe PubMed Central

PubMed publication ID

28 September 2017

Bin Hu

3

1 reference

Europe PubMed Central

PubMed publication ID

28 September 2017

Wenjuan Zhu

4

1 reference

Europe PubMed Central

PubMed publication ID

28 September 2017

Qibin Li

5

1 reference

Europe PubMed Central

PubMed publication ID

28 September 2017

Ping Yuan

6

1 reference

Europe PubMed Central

PubMed publication ID

28 September 2017

Xinyuan Guan

8

1 reference

Europe PubMed Central

PubMed publication ID

28 September 2017

Fucheng Li

9

1 reference

Europe PubMed Central

PubMed publication ID

28 September 2017

Xiangyi Jing

10

1 reference

Europe PubMed Central

PubMed publication ID

28 September 2017

Ru Li

11

1 reference

Europe PubMed Central

PubMed publication ID

28 September 2017

Yongling Zhang

12

1 reference

Europe PubMed Central

PubMed publication ID

28 September 2017

Claude Férec

13

1 reference

Europe PubMed Central

PubMed publication ID

28 September 2017

Dongsheng Huang

16

1 reference

Europe PubMed Central

PubMed publication ID

28 September 2017

Jian-Min Chen

17

1 reference

Europe PubMed Central

PubMed publication ID

28 September 2017

Yiming Wang

18

1 reference

Europe PubMed Central

PubMed publication ID

28 September 2017

publication date

20 March 2015

1 reference

Europe PubMed Central

PubMed publication ID

28 September 2017

1 reference

Europe PubMed Central

PubMed publication ID

28 September 2017

134

1 reference

Europe PubMed Central

PubMed publication ID

28 September 2017

6

1 reference

Europe PubMed Central

PubMed publication ID

28 September 2017

589-603

1 reference

Europe PubMed Central

PubMed publication ID

28 September 2017

CNVnator: an approach to discover, genotype, and characterize typical and atypical CNVs from family and population genome sequencing

1 reference

https://api.crossref.org/works/10.1007%2FS00439-015-1539-4

21 January 2018

De novo CNV formation in mouse embryonic stem cells occurs in the absence of Xrcc4-dependent nonhomologous end joining

1 reference

https://api.crossref.org/works/10.1007%2FS00439-015-1539-4

21 January 2018

Genomic rearrangements in the CFTR gene: extensive allelic heterogeneity and diverse mutational mechanisms

1 reference

https://api.crossref.org/works/10.1007%2FS00439-015-1539-4

21 January 2018

Multiple osteochondromas

1 reference

https://api.crossref.org/works/10.1007%2FS00439-015-1539-4

21 January 2018

Mutation spectrum of Drosophila CNVs revealed by breakpoint sequencing.

1 reference

https://api.crossref.org/works/10.1007%2FS00439-015-1539-4

21 January 2018

Replicative mechanisms for CNV formation are error prone

1 reference

https://api.crossref.org/works/10.1007%2FS00439-015-1539-4

21 January 2018

Gene conversion: mechanisms, evolution and human disease

1 reference

https://api.crossref.org/works/10.1007%2FS00439-015-1539-4

21 January 2018

BreakDancer: an algorithm for high-resolution mapping of genomic structural variation

1 reference

https://api.crossref.org/works/10.1007%2FS00439-015-1539-4

21 January 2018

Genomic rearrangements in inherited disease and cancer

1 reference

https://api.crossref.org/works/10.1007%2FS00439-015-1539-4

21 January 2018

Patterns and mutational signatures of tandem base substitutions causing human inherited disease

1 reference

https://api.crossref.org/works/10.1007%2FS00439-015-1539-4

21 January 2018

Mutation spectrum revealed by breakpoint sequencing of human germline CNVs

1 reference

https://api.crossref.org/works/10.1007%2FS00439-015-1539-4

21 January 2018

A time-invariant principle of genome evolution

1 reference

https://api.crossref.org/works/10.1007%2FS00439-015-1539-4

21 January 2018

Break-induced replication is highly inaccurate

1 reference

https://api.crossref.org/works/10.1007%2FS00439-015-1539-4

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-015-1539-4

21 January 2018

A microhomology-mediated break-induced replication model for the origin of human copy number variation

1 reference

https://api.crossref.org/works/10.1007%2FS00439-015-1539-4

21 January 2018

Increased mutagenesis and unique mutation signature associated with mitotic gene conversion

1 reference

https://api.crossref.org/works/10.1007%2FS00439-015-1539-4

21 January 2018

More single-nucleotide mutations surround small insertions than small deletions in primates.

1 reference

https://api.crossref.org/works/10.1007%2FS00439-015-1539-4

21 January 2018

Recovery of arrested replication forks by homologous recombination is error-prone

1 reference

https://api.crossref.org/works/10.1007%2FS00439-015-1539-4

21 January 2018

Detection of clinically relevant genetic variants in autism spectrum disorder by whole-genome sequencing

1 reference

https://api.crossref.org/works/10.1007%2FS00439-015-1539-4

21 January 2018

Fine-scale signatures of molecular evolution reconcile models of indel-associated mutation

1 reference

https://api.crossref.org/works/10.1007%2FS00439-015-1539-4

21 January 2018

Transcript-RNA-templated DNA recombination and repair

1 reference

https://api.crossref.org/works/10.1007%2FS00439-015-1539-4

21 January 2018

A human genome structural variation sequencing resource reveals insights into mutational mechanisms

1 reference

https://api.crossref.org/works/10.1007%2FS00439-015-1539-4

21 January 2018

Fast and accurate short read alignment with Burrows-Wheeler transform

1 reference

https://api.crossref.org/works/10.1007%2FS00439-015-1539-4

21 January 2018

The Sequence Alignment/Map format and SAMtools

1 reference

https://api.crossref.org/works/10.1007%2FS00439-015-1539-4

21 January 2018

The mechanism of human nonhomologous DNA end joining

1 reference

https://api.crossref.org/works/10.1007%2FS00439-015-1539-4

21 January 2018

Chromosome catastrophes involve replication mechanisms generating complex genomic rearrangements

1 reference

https://api.crossref.org/works/10.1007%2FS00439-015-1539-4

21 January 2018

MMEJ repair of double-strand breaks (director's cut): deleted sequences and alternative endings

1 reference

https://api.crossref.org/works/10.1007%2FS00439-015-1539-4

21 January 2018

Repair of DNA double-strand breaks by templated nucleotide sequence insertions derived from distant regions of the genome

1 reference

https://api.crossref.org/works/10.1007%2FS00439-015-1539-4

21 January 2018

DELLY: structural variant discovery by integrated paired-end and split-read analysis

1 reference

https://api.crossref.org/works/10.1007%2FS00439-015-1539-4

21 January 2018

Role of DNA polymerases in repeat-mediated genome instability

1 reference

https://api.crossref.org/works/10.1007%2FS00439-015-1539-4

21 January 2018

Template switching during break-induced replication

1 reference

https://api.crossref.org/works/10.1007%2FS00439-015-1539-4

21 January 2018

Integrative Genomics Viewer (IGV): high-performance genomics data visualization and exploration

1 reference

https://api.crossref.org/works/10.1007%2FS00439-015-1539-4

21 January 2018

Single-nucleotide mutation rate increases close to insertions/deletions in eukaryotes.

1 reference

https://api.crossref.org/works/10.1007%2FS00439-015-1539-4

21 January 2018

The fine-scale architecture of structural variants in 17 mouse genomes

1 reference

https://api.crossref.org/works/10.1007%2FS00439-015-1539-4

21 January 2018

Complex gene rearrangements caused by serial replication slippage

1 reference

https://api.crossref.org/works/10.1007%2FS00439-015-1539-4

21 January 2018

Closely spaced multiple mutations as potential signatures of transient hypermutability in human genes

1 reference

https://api.crossref.org/works/10.1007%2FS00439-015-1539-4

21 January 2018

Easy calculations of lod scores and genetic risks on small computers

1 reference

https://pubmed.ncbi.nlm.nih.gov/25792359

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00439-015-1539-4

1 reference

Europe PubMed Central

PubMed publication ID

28 September 2017

Dimensions Publication ID

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

28 September 2017

ResearchGate publication ID

0 references

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q41190098&oldid=2270294284"