Rare copy number variant analysis in case–control studies using snp array data: a scalable and automated data analysis pipeline
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- Extent
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1 Online-Ressource.
- Language
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Englisch
- Bibliographic citation
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Rare copy number variant analysis in case–control studies using snp array data: a scalable and automated data analysis pipeline ; volume:25 ; number:1 ; day:15 ; month:11 ; year:2024 ; pages:1-13 ; date:12.2024
BMC bioinformatics ; 25, Heft 1 (15.11.2024), 1-13, 12.2024
- Creator
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Artaza, Haydee
Lavrichenko, Ksenia
Wolff, Anette S. B.
Røyrvik, Ellen C.
Vaudel, Marc
Johansson, Stefan
- Contributor
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SpringerLink (Online service)
- DOI
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10.1186/s12859-024-05979-0
- URN
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urn:nbn:de:101:1-2502040848423.571471974788
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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15.08.2025, 7:27 AM CEST
Data provider
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Associated
- Artaza, Haydee
- Lavrichenko, Ksenia
- Wolff, Anette S. B.
- Røyrvik, Ellen C.
- Vaudel, Marc
- Johansson, Stefan
- SpringerLink (Online service)
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SNP and gene networks construction and analysis from classification of copy number variations data
Bivariate segmentation of SNP-array data for allele-specific copy number analysis in tumour samples
SNP HiTLink: a high-throughput linkage analysis system employing dense SNP data
Major copy proportion analysis of tumor samples using SNP arrays
Advanced memory data structures for scalable event trace analysis
Scalable data profiling : distributed discovery and analysis of structural metadata
An integrated Bayesian analysis of LOH and copy number data
Scalable Data Integration for Linked Data
Cluster Analysis : A Comparison of Different Similarity Measures for SNP Data
Multilocus analysis of SNP and metabolic data within a given pathway
Cluster Analysis : A Comparision of Different Similarity Measures for SNP Data