Algorithm implementation for CNV discovery using Affymetrix and Illumina SNP array data.
SNP array data can be analysed for the purpose of calling SNP alleles but also for determining the absolute copy number of a certain genomic segment. Here, the method for detecting copy number (CN) change using intensity data from SNP arrays is focused on. Methods incorporating data from the two mai...
Asıl Yazarlar: | Winchester, L, Ragoussis, J |
---|---|
Materyal Türü: | Journal article |
Dil: | English |
Baskı/Yayın Bilgisi: |
2012
|
Benzer Materyaller
-
Comparing CNV detection methods for SNP arrays.
Yazar:: Winchester, L, ve diğerleri
Baskı/Yayın Bilgisi: (2009) -
CNV discovery using SNP genotyping arrays.
Yazar:: Yau, C, ve diğerleri
Baskı/Yayın Bilgisi: (2008) -
Detection, breakpoint identification and detailed characterisation of a CNV at the FRA16D site using SNP assays.
Yazar:: Winchester, L, ve diğerleri
Baskı/Yayın Bilgisi: (2008) -
Hybridization and amplification rate correction for affymetrix SNP arrays
Yazar:: Wang Quan, ve diğerleri
Baskı/Yayın Bilgisi: (2012-06-01) -
Whole genome sequencing of simmental cattle for SNP and CNV discovery
Yazar:: Ting Sun, ve diğerleri
Baskı/Yayın Bilgisi: (2023-04-01)