SLOPE: a quick and accurate method for locating non-SNP structural variation from targeted next-generation sequence data
Work
Year: 2010
Type: article
Abstract: Motivation: Targeted ‘deep’ sequencing of specific genes or regions is of great interest in clinical cancer diagnostics where some sequence variants, particularly translocations and indels, have know... more
Source: Bioinformatics
Institutions Washington University in St. Louis, University of Utah, Cofactor Genomics (United States)
Cites: 17
Cited by: 56
Related to: 10
FWCI: 2.93
Citation percentile (by year/subfield): 77.69
Subfield: Molecular Biology
Domain: Life Sciences
Open Access status: bronze