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Statistical model-based testing to evaluate the recurrence of genomic aberrations.
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scholarly article
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stated in
Europe PubMed Central
PMC publication ID
3371835
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22689750%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 February 2020
title
Statistical model-based testing to evaluate the recurrence of genomic aberrations
(English)
1 reference
stated in
Europe PubMed Central
PMC publication ID
3371835
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22689750%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 February 2020
main subject
statistics
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author
Teppei Shimamura
series ordinal
3
1 reference
stated in
Europe PubMed Central
PMC publication ID
3371835
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22689750%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 February 2020
author name string
Atushi Niida
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMC publication ID
3371835
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22689750%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 February 2020
Seiya Imoto
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2
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Europe PubMed Central
PMC publication ID
3371835
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22689750%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 February 2020
Satoru Miyano
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4
1 reference
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Europe PubMed Central
PMC publication ID
3371835
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22689750%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 February 2020
language of work or name
English
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publication date
1 June 2012
1 reference
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Europe PubMed Central
PMC publication ID
3371835
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22689750%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 February 2020
published in
Bioinformatics
1 reference
stated in
Europe PubMed Central
PMC publication ID
3371835
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22689750%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 February 2020
volume
28
1 reference
stated in
Europe PubMed Central
PMC publication ID
3371835
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22689750%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 February 2020
issue
12
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Europe PubMed Central
PMC publication ID
3371835
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22689750%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 February 2020
page(s)
i115-20
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Europe PubMed Central
PMC publication ID
3371835
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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22689750%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 February 2020
copyright license
Creative Commons Attribution-NonCommercial 3.0 Unported
start time
2 October 2016
1 reference
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April 2023 Public Data File from Crossref
copyright status
copyrighted
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cites work
A map of human genome variation from population-scale sequencing
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3371835
retrieved
11 September 2017
Advances in understanding cancer genomes through second-generation sequencing
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3371835
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11 September 2017
SNP array analysis in hematologic malignancies: avoiding false discoveries
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11 September 2017
The landscape of somatic copy-number alteration across human cancers
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PubMed Central
reference URL
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retrieved
11 September 2017
PICNIC: an algorithm to predict absolute allelic copy number variation with microarray cancer data
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3371835
retrieved
11 September 2017
Segmentation-based detection of allelic imbalance and loss-of-heterozygosity in cancer cells using whole genome SNP arrays
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PubMed Central
reference URL
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11 September 2017
Assessing the significance of chromosomal aberrations in cancer: methodology and application to glioma
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3371835
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11 September 2017
Detection of DNA copy number alterations in cancer by array comparative genomic hybridization
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3371835
retrieved
11 September 2017
Assessing the significance of conserved genomic aberrations using high resolution genomic microarrays
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3371835
retrieved
11 September 2017
Highly sensitive method for genomewide detection of allelic composition in nonpaired, primary tumor specimens by use of affymetrix single-nucleotide-polymorphism genotyping microarrays
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3371835
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11 September 2017
A faster circular binary segmentation algorithm for the analysis of array CGH data
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3371835
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11 September 2017
Inferring loss-of-heterozygosity from unpaired tumors using high-density oligonucleotide SNP arrays
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3371835
retrieved
11 September 2017
Signatures of mutation and selection in the cancer genome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3371835
retrieved
14 September 2017
Finding recurrent copy number alterations preserving within-sample homogeneity
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3371835
retrieved
21 August 2018
Identifiers
DOI
10.1093/BIOINFORMATICS/BTS203
1 reference
stated in
Europe PubMed Central
PMC publication ID
3371835
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22689750%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 February 2020
DBLP publication ID
journals/bioinformatics/NiidaISM12
1 reference
stated in
DBLP Dataset 2021-01-02
retrieved
28 January 2021
PMC publication ID
3371835
1 reference
stated in
Europe PubMed Central
PMC publication ID
3371835
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22689750%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 February 2020
PubMed publication ID
22689750
1 reference
stated in
Europe PubMed Central
PMC publication ID
3371835
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22689750%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 February 2020
ResearchGate publication ID
225293557
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