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Copy number variation detection using next generation sequencing read counts.
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scholarly article
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Europe PubMed Central
PMC publication ID
4021345
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24731174%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 March 2020
title
Copy number variation detection using next generation sequencing read counts
(English)
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stated in
Europe PubMed Central
PMC publication ID
4021345
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24731174%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 March 2020
author
Dan Nettleton
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2
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Europe PubMed Central
PMC publication ID
4021345
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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24731174%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 March 2020
author name string
Heng Wang
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1
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Europe PubMed Central
PMC publication ID
4021345
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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24731174%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 March 2020
Kai Ying
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3
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Europe PubMed Central
PMC publication ID
4021345
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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24731174%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 March 2020
publication date
14 April 2014
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Europe PubMed Central
PMC publication ID
4021345
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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24731174%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 March 2020
published in
BMC Bioinformatics
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Europe PubMed Central
PMC publication ID
4021345
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24731174%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 March 2020
volume
15
1 reference
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Europe PubMed Central
PMC publication ID
4021345
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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24731174%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 March 2020
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109
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Europe PubMed Central
PMC publication ID
4021345
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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24731174%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 March 2020
copyright license
Creative Commons Attribution 2.0 Generic
start time
14 April 2014
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April 2022 Public Data File from Crossref
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copyrighted
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April 2022 Public Data File from Crossref
describes a project that uses
massive parallel sequencing
1 reference
based on heuristic
inferred from title
exact match
https://scigraph.springernature.com/pub.10.1186/1471-2105-15-109
0 references
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14 July 2018
Comparing next-generation sequencing and microarray technologies in a toxicological study of the effects of aristolochic acid on rat kidneys
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14 July 2018
A computational framework discovers new copy number variants with functional importance
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14 July 2018
CNVnator: an approach to discover, genotype, and characterize typical and atypical CNVs from family and population genome sequencing
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14 July 2018
Detecting common copy number variants in high-throughput sequencing data by using JointSLM algorithm
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14 July 2018
Pervasive gene content variation and copy number variation in maize and its undomesticated progenitor
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14 July 2018
CNAseg--a novel framework for identification of copy number changes in cancer from second-generation sequencing data.
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14 July 2018
rSW-seq: algorithm for detection of copy number alterations in deep sequencing data
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14 July 2018
A first-generation haplotype map of maize
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14 July 2018
The B73 Maize Genome: Complexity, Diversity, and Dynamics
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Maize inbreds exhibit high levels of copy number variation (CNV) and presence/absence variation (PAV) in genome content
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14 July 2018
Computational methods for discovering structural variation with next-generation sequencing
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14 July 2018
Statistical issues in the analysis of DNA Copy Number Variations
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14 July 2018
Sensitive and accurate detection of copy number variants using read depth of coverage
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14 July 2018
Copy number variants (CNVs) in primate species using array-based comparative genomic hybridization.
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Allelic genome structural variations in maize detected by array comparative genome hybridization
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BreakDancer: an algorithm for high-resolution mapping of genomic structural variation
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An inequality with applications to statistical estimation for probabilistic functions of Markov processes and to a model for ecology
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retrieved
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https://opencitations.net/index/coci/api/v1/citations/10.1090/S0002-9904-1967-11751-8
Identifiers
DOI
10.1186/1471-2105-15-109
1 reference
stated in
Europe PubMed Central
PMC publication ID
4021345
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24731174%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 March 2020
DBLP publication ID
journals/bmcbi/WangNY14
1 reference
stated in
DBLP Dataset 2021-01-02
retrieved
28 January 2021
PMC publication ID
4021345
1 reference
stated in
Europe PubMed Central
PMC publication ID
4021345
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24731174%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 March 2020
PubMed publication ID
24731174
1 reference
stated in
Europe PubMed Central
PMC publication ID
4021345
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24731174%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 March 2020
ResearchGate publication ID
261732692
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