- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
1750-1172
- Extent
-
Online-Ressource
- Language
-
Englisch
- Notes
-
online resource.
- Bibliographic citation
-
Understanding the impact of 1q21.1 copy number variant ; volume:6 ; number:1 ; day:8 ; month:8 ; year:2011 ; pages:1-12 ; date:12.2011
Orphanet journal of rare diseases ; 6, Heft 1 (8.8.2011), 1-12, 12.2011
- Creator
-
Harvard, Chansonette
- Contributor
-
Strong, Emma
Mercier, Eloi
Colnaghi, Rita
Alcantara, Diana
Chow, Eva
Martell, Sally
Tyson, Christine
Hrynchak, Monica
McGillivray, Barbara
Hamilton, Sara
Marles, Sandra
Mhanni, Aziz
Dawson, Angelika J.
Pavlidis, Paul
Qiao, Ying
Holden, Jeanette J.
Lewis, Suzanne ME
O'Driscoll, Mark
Rajcan-Separovic, Evica
SpringerLink (Online service)
- DOI
-
10.1186/1750-1172-6-54
- URN
-
urn:nbn:de:1111-2016050119603
- Rights
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
14.08.2025, 11:02 AM CEST
Data provider
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Associated
- Harvard, Chansonette
- Strong, Emma
- Mercier, Eloi
- Colnaghi, Rita
- Alcantara, Diana
- Chow, Eva
- Martell, Sally
- Tyson, Christine
- Hrynchak, Monica
- McGillivray, Barbara
- Hamilton, Sara
- Marles, Sandra
- Mhanni, Aziz
- Dawson, Angelika J.
- Pavlidis, Paul
- Qiao, Ying
- Holden, Jeanette J.
- Lewis, Suzanne ME
- O'Driscoll, Mark
- Rajcan-Separovic, Evica
- SpringerLink (Online service)
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MCKAT: a multi-dimensional copy number variant kernel association test
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Prediction of a deletion copy number variant by a dense SNP panel
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DECA: scalable XHMM exome copy-number variant calling with ADAM and Apache Spark
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