Comparison of kNN and k-means optimization methods of reference set selection for improved CNV callers performance.

ABSTRACT:

Background

There are over 25 tools dedicated for the detection of Copy Number Variants (CNVs) using Whole Exome Sequencing (WES) data based on read depth analysis. The tools reported consist of several steps, including: (i) calculation of read depth for each sequencing target, (ii) normalization, (iii) segmentation and (iv) actual CNV calling. The essential aspect of the entire process is the normalization stage, in which systematic errors and biases are removed and the reference sample set is used to increase the signal-to-noise ratio. Although some CNV calling tools use dedicated algorithms to obtain the optimal reference sample set, most of the advanced CNV callers do not include this feature. To our knowledge, this work is the first attempt to assess the impact of reference sam

SUBMITTER: Kusmirek W 

PROVIDER: S-EPMC6537193 | biostudies-literature | 2019 May

REPOSITORIES: biostudies-literature