Effect of Combining Multiple CNV Defining Algorithms on the Reliability of CNV Calls from SNP Genotyping Data
In addition to single-nucleotide polymorphisms (SNP), copy number variation (CNV) is a major component of human genetic diversity. Among many whole-genome analysis platforms, SNP arrays have been commonly used for genomewide CNV discovery. Recently, a number of CNV defining algorithms from SNP genot...
Saved in:
Main Authors: | Soon-Young Kim, Ji-Hong Kim, Yeun-Jun Chung |
---|---|
Format: | Article |
Language: | English |
Published: |
BioMed Central
2012-09-01
|
Series: | Genomics & Informatics |
Subjects: | |
Online Access: | http://genominfo.org/upload/pdf/gni-10-194.pdf |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
A case of iatrogenic CNV following macular surgery
by: Akshay Prashant Agnihotri, et al.
Published: (2025-03-01) -
Web-Based Database and Viewer of East Asian Copy Number Variations
by: Ji-Hong Kim, et al.
Published: (2012-03-01) -
Identifying Copy Number Variants under Selection in Geographically Structured Populations Based on -statistics
by: Hae-Hiang Song, et al.
Published: (2012-06-01) -
Genome Architecture and Its Roles in Human Copy Number Variation
by: Lu Chen, et al.
Published: (2014-12-01) -
SNP-array profiling data from breast cancer patients and healthy women's blood DNA samplesGEO
by: Rafika Indah Paramita, et al.
Published: (2025-04-01)