- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
1297-9686
- Extent
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Online-Ressource
- Language
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Englisch
- Notes
-
online resource.
- Bibliographic citation
-
Prediction of a deletion copy number variant by a dense SNP panel ; volume:44 ; number:1 ; day:23 ; month:3 ; year:2012 ; pages:1-9 ; date:12.2012
Genetics, selection, evolution ; 44, Heft 1 (23.3.2012), 1-9, 12.2012
- Creator
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Kadri, Naveen K.
- Contributor
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Koks, Patrick D.
Meuwissen, Theo H E.
SpringerLink (Online service)
- DOI
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10.1186/1297-9686-44-7
- URN
-
urn:nbn:de:1111-201603252817
- Rights
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
14.08.2025, 10:47 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Kadri, Naveen K.
- Koks, Patrick D.
- Meuwissen, Theo H E.
- SpringerLink (Online service)
Other Objects (12)
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Major copy proportion analysis of tumor samples using SNP arrays
Understanding the impact of 1q21.1 copy number variant
SNP genotyping to screen for a common deletion in CHARGE Syndrome
Evaluation of copy number variation detection for a SNP array platform
Comments on Tue Trinh (2009) : A constraint on copy deletion
New cytogenetically visible copy number variant in region 8q21.2
Accuracy of breeding values of 'unrelated' individuals predicted by dense SNP genotyping
Genomic predictions combining SNP markers and copy number variations in Nellore cattle
Identification of copy number variations and common deletion polymorphisms in cattle
MCKAT: a multi-dimensional copy number variant kernel association test
SNP HiTLink: a high-throughput linkage analysis system employing dense SNP data
Rare copy number variant analysis in case–control studies using snp array data: a scalable and automated data analysis pipeline
Major copy proportion analysis of tumor samples using SNP arrays
Understanding the impact of 1q21.1 copy number variant
SNP genotyping to screen for a common deletion in CHARGE Syndrome
Evaluation of copy number variation detection for a SNP array platform
Comments on Tue Trinh (2009) : A constraint on copy deletion
New cytogenetically visible copy number variant in region 8q21.2
Accuracy of breeding values of 'unrelated' individuals predicted by dense SNP genotyping
Genomic predictions combining SNP markers and copy number variations in Nellore cattle
Identification of copy number variations and common deletion polymorphisms in cattle
MCKAT: a multi-dimensional copy number variant kernel association test
SNP HiTLink: a high-throughput linkage analysis system employing dense SNP data
Rare copy number variant analysis in case–control studies using snp array data: a scalable and automated data analysis pipeline
Major copy proportion analysis of tumor samples using SNP arrays
Understanding the impact of 1q21.1 copy number variant
SNP genotyping to screen for a common deletion in CHARGE Syndrome
Evaluation of copy number variation detection for a SNP array platform
Comments on Tue Trinh (2009) : A constraint on copy deletion
New cytogenetically visible copy number variant in region 8q21.2
Accuracy of breeding values of 'unrelated' individuals predicted by dense SNP genotyping
Genomic predictions combining SNP markers and copy number variations in Nellore cattle
Identification of copy number variations and common deletion polymorphisms in cattle