Detection and reconstruction of tandemly organized de novo copy number variations

BMC Bioinformatics

Research

Nicholas Furlotte¹  Dan He¹  Eleazar Eskin¹ 

[1] Dept. of Comp. Sci., Univ. of California Los Angeles, 90095, Los Angeles, CA, USA;

关键词: Copy Number Variation;    Coverage Ratio;    Donor Genome;    Copy Number Variation Region;    Discordant Pair;   

DOI  :  10.1186/1471-2105-11-S11-S12

来源: Springer

【 摘 要 】

BackgroundThe characterization of structural variations (SV) such as insertions, deletions and copy number variations is a critical step in the process of understanding the full genetic architecture of organisms. Copy number variations (CNV) have attracted much recent attention due to their effects on gene expression and disease status.ResultsIn this paper, we present a method that utilizes next-generation sequencing technologies (NGS), in order to both detect and reconstruct CNVs. We focus on a special type of CNV, namely tandemly organized de novo CNVs, which have been shown to occur with high frequency in the mouse genome.ConclusionsWe apply our method to CNV regions randomly inserted into the reference mouse genome and show that our method achieves good performance for both detection and reconstruction of tandemly organized de novo CNVs.

【 授权许可】

CC BY   
© He et al; licensee BioMed Central Ltd. 2010