Structural variation in the human genome
By L. Feuk, A. Carson, Stephen W. Scherer. Nature reviews genetics, 2006
947 citations recorded by the source corpus.
Subfields: Genetics, Plant Science
View Paper: https://www.semanticscholar.org/paper/25be15abdece252135e4449136e10c03682a4162
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
In Genetics
- David Haussler
- W. James Kent
- Eric J. Topol
- Paul Medvedev
- Nicholas J. Schork
- Masatoshi Nei
- Benedict Paten
- Jonathan Sebat
In Plant Science
- David Haussler
- W. James Kent
- Robert M. Kuhn
- Kate R. Rosenbloom
- A. Hinrichs
- Donna Karolchik
- Mark Diekhans
- Brian J. Raney
Citations in the corpus
- Computational methods for discovering structural variation with next-generation sequencing (2009, background): “as an important contributor to heterozygosity has revolutionized our understanding of the landscape of human genotypes (for an introduction, see ref”
- Sensitive and accurate detection of copy number variants using read depth of coverage. (2009, background): “Structural variants (SVs) in the human genome (Iafrate et al. 2004; Sebat et al. 2004; Feuk et al. 2006a), including copy number variants (CNVs) and balanced rearrangements such as inversions and translocations, play an important role in the genetics of complex disease.”
- The evolution of animal chemosensory receptor gene repertoires: roles of chance and necessity (2008, background): “have studied the extent of copy-number variation in various regions of the human genome (see Ref”
- BreakDancer: An algorithm for high resolution mapping of genomic structural variation (2009, neutral): “1363" language="eng" relation="no"> Genomic structural variation is commonly considered to be any DNA sequence alteration other than a single nucleotide substitutio”
- Human genetic variation and its contribution to complex traits (2009, background): “There have been several excellent reviews on structural variatio”
- The UCSC Genome Browser Database: 2008 update (2007, methodology): “The Structural Variation annotation has been expanded to include structural variation data (17), deletions detected by several techniques (18–20) and numerous copy number polymorphism data sets (21–25).”
- The UCSC Genome Browser database: update 2011 (2010, background): “The Database of Genomic Variants (DGV) (29,30) tracks, which detail genomic variants found among healthy human individuals, were updated to version 9 in the hg17 and hg18 assemblies and added to the hg19 assembly browser.”