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...
Hlavní autoři: | Winchester, L, Ragoussis, J |
---|---|
Médium: | Journal article |
Jazyk: | English |
Vydáno: |
2012
|
Podobné jednotky
-
Comparing CNV detection methods for SNP arrays.
Autor: Winchester, L, a další
Vydáno: (2009) -
CNV discovery using SNP genotyping arrays.
Autor: Yau, C, a další
Vydáno: (2008) -
Detection, breakpoint identification and detailed characterisation of a CNV at the FRA16D site using SNP assays.
Autor: Winchester, L, a další
Vydáno: (2008) -
Whole genome sequencing of simmental cattle for SNP and CNV discovery
Autor: Ting Sun, a další
Vydáno: (2023-04-01) -
Effect of Combining Multiple CNV Defining Algorithms on the Reliability of CNV Calls from SNP Genotyping Data
Autor: Soon-Young Kim, a další
Vydáno: (2012-09-01)