Somatic mosaicism for copy-neutral loss of heterozygosity and DNA copy number variations in the human genome (Q28388948)

6

object named as

Andres Salumets

0 references

Ants Kurg

object named as

Ants Kurg

4

0 references

Marina Koltšina

2

object named as

Marina Koltšina

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author name string

Olga Žilina

1

0 references

Raivo Raid

3

0 references

Neeme Tõnisson

Creative Commons Attribution 4.0 International

5

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language of work or name

English

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publication date

16 September 2015

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published in

BMC Genomics

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volume

16

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issue

1

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page(s)

703

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copyright license

start time

16 September 2015

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

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29 September 2017

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Genome-wide SNP assay reveals structural genomic variation, extended homozygosity and cell-line induced alterations in normal individuals

29 September 2017

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29 September 2017

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29 September 2017

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Extended tracts of homozygosity in outbred human populations

29 September 2017

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Crossref

https://api.crossref.org/works/10.1186%2FS12864-015-1916-3

CNV Concordance in 1,097 MZ Twin Pairs.

21 January 2018

1 reference

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Large Autosomal Copy-Number Differences within Unselected Monozygotic Twin Pairs are Rare

27 November 2018

1 reference

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Long contiguous stretches of homozygosity in the human genome

27 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/26376747

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Somatic mosaicism for copy number variation in differentiated human tissues

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/26376747

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1186/S12864-015-1916-3

1 reference

Dimensions Publication ID

1 reference

9 September 2019

https://scigraph.springernature.com/pub.10.1186/s12864-015-1916-3

1 reference

1 reference

PubMed publication ID

26376747

1 reference