Identification of Medium-Sized Copy Number Alterations in Whole-Genome Sequencing. (January 2014)

• Record Type: Journal Article
• Authors: Ozer, Hatice Gulcin; Usubalieva, Aisulu; Dorrance, Adrienne; Yilmaz, Ayse Selen; Caligiuri, Michael; Marcucci, Guido; Huang, Kun
• Is Part Of: Cancer informatics. Volume 13(2014)Supplement 3
• Publication Date: 2014-01
• Subjects: copy number alteration (CNA) -- whole-genome sequencing -- acute myeloid leukemia (AML); Bioinformatics -- Periodicals; Biology -- Data processing -- Periodicals; Cancer -- Periodicals; Cancer -- Research -- Periodicals; Computational biology -- Periodicals; 570.285
• DOI: 10.4137/CIN.S14023
• Languages: English
• ISSNs: 1176-9351

Abstract

The genome-wide discoveries such as detection of copy number alterations (CNA) from high-throughput whole-genome sequencing data enabled new developments in personalized medicine. The CNAs have been reported to be associated with various diseases and cancers including acute myeloid leukemia. However, there are multiple challenges to the use of current CNA detection tools that lead to high false-positive rates and thus impede widespread use of such tools in cancer research. In this paper, we discuss these issues and propose possible solutions. First, since the entire genome cannot be mapped due to some regions lacking sequence uniqueness, current methods cannot be appropriately adjusted to handle these regions in the analyses. Thus, detection of medium-sized CNAs is also being directly affected by these mappability problems. The requirement for matching control samples is also an important limitation because acquiring matching controls might not be possible or might not be cost efficient. Here we present an approach that addresses these issues and detects medium-sized CNAs in cancer genomes by (1) masking unmappable regions during the initial CNA detection phase, (2) using pool of a few normal samples as control, and (3) employing median filtering to adjust CNA ratios to its surrounding coverage and eliminate false positives.