A computational framework with simulation-based error models for inferring genomic structural variants from massive paired-end sequencing data.
Mar 5, 2012 · A specifically engineered algorithm then enumerates all max-cliques and statistically evaluates them for their potential to reflect insertions or deletions ( ...
Nov 15, 2012 · A novel algorithm then enumerates all max-cliques and statistically evaluates them for their potential to reflect insertions or deletions. For ...
A novel internal segment size based approach is presented, which organizes all, including concordant, reads into a read alignment graph, where max-cliques ...
A novel algorithm then enumerates all max-cliques and statistically evaluates them for their potential to reflect insertions or deletions. For the first time in ...
A specifically engineered algorithm then enumerates all max-cliques and statistically evaluates them for their potential to reflect insertions or deletions ( ...
Motivation: Next-generation sequencing techniques have facilitated a large-scale analysis of human genetic variation. Despite the advances in sequencing ...
A novel algorithm then enumerates all max-cliques and statistically evaluates them for their potential to reflect insertions or deletions. For the first time in ...
Title. CLEVER: clique-enumerating variant finder. Authors. Marschall, Tobias; Costa, Ivan G; Canzar, Stefan; Bauer, Markus; Klau, Gunnar W; Schliep, ...
This paper describes a software package, CLEVER (Accessed 22 Aug 2013), to detect likely insertions and deletions (indels) from paired-end ...