TY - JOUR
T1 - SnoopCGH
T2 - Software for visualizing comparative genomic hybridization data
AU - Almagro-Gracia, Jacob
AU - Manske, Magnus
AU - Carret, Celine
AU - Campino, Susana
AU - Auburn, Sarah
AU - MacInnis, Bronwyn
AU - Maslen, Gareth
AU - Pain, Arnab
AU - Newbold, Christopher
AU - Kwiatkowski, Dominic
AU - Clark, Taane
PY - 2009
Y1 - 2009
N2 - Array-based comparative genomic hybridization (CGH) technology is used to discover and validate genomic structural variation, including copy number variants, insertions, deletions and other structural variants (SVs). The visualization and summarization of the array CGH data outputs, potentially across many samples, is an important process in the identification and analysis of SVs. We have developed a software tool for SV analysis using data from array CGH technologies, which is also amenable to short-read sequence data.
AB - Array-based comparative genomic hybridization (CGH) technology is used to discover and validate genomic structural variation, including copy number variants, insertions, deletions and other structural variants (SVs). The visualization and summarization of the array CGH data outputs, potentially across many samples, is an important process in the identification and analysis of SVs. We have developed a software tool for SV analysis using data from array CGH technologies, which is also amenable to short-read sequence data.
UR - http://www.scopus.com/inward/record.url?scp=70349978985&partnerID=8YFLogxK
M3 - Article
SN - 1367-4803
VL - 25
SP - 2732
EP - 2733
JO - Bioinformatics
JF - Bioinformatics
IS - 20
ER -