iCopyDAV: Integrated platform for copy number variations-Detection, annotation and visualization.
Discovery of copy number variations (CNVs), a major category of structural variations, have dramatically changed our understanding of differences between individuals and provide an alternate paradigm for the genetic basis of human diseases. CNVs include both copy gain and copy loss events and their...
Main Authors: | Prashanthi Dharanipragada, Sriharsha Vogeti, Nita Parekh |
---|---|
Format: | Article |
Language: | English |
Published: |
Public Library of Science (PLoS)
2018-01-01
|
Series: | PLoS ONE |
Online Access: | http://europepmc.org/articles/PMC5886540?pdf=render |
Similar Items
-
HandyCNV: Standardized Summary, Annotation, Comparison, and Visualization of Copy Number Variant, Copy Number Variation Region, and Runs of Homozygosity
by: Jinghang Zhou, et al.
Published: (2021-09-01) -
SeqVItA: Sequence Variant Identification and Annotation Platform for Next Generation Sequencing Data
by: Prashanthi Dharanipragada, et al.
Published: (2018-11-01) -
aCNViewer: Comprehensive genome-wide visualization of absolute copy number and copy neutral variations.
by: Victor Renault, et al.
Published: (2017-01-01) -
CNVannotator: a comprehensive annotation server for copy number variation in the human genome.
by: Min Zhao, et al.
Published: (2013-01-01) -
Copy number variation and schizophrenia
by: Tam, Gloria Wing Chi
Published: (2009)