Jul 18, 2022 · Abstract. Advances in whole-genome sequencing (WGS) promise to enable the accurate and comprehensive structural variant (SV) discovery.
We benchmarked currently available whole-genome sequencing (WGS)-based SV callers to determine the efficacy of available tools and find methods with a good ...
Sep 17, 2020 · Structural variants (SVs) are genomic regions that contain an altered DNA sequence due to deletion, duplication, insertion, or inversion. SVs ...
Abstract. Advances in whole-genome sequencing (WGS) promise to enable the accurate and comprehensive structural variant (SV) discovery. Dissecting SVs from.
Our study investigates the ability of the methods to detect deletions, thus providing an optimistic estimate of SV detection performance, as the SV-detection ...
May 26, 2020 · Our study investigates the ability of the methods to detect deletions, thus providing an optimistic estimate of SV detection performance, as the ...
2013. TLDR. iSVP, a new deletion calling pipeline to obtain a genome-wide landscape of deletions in a highly accurate manner, is presented and it is shown ...
Abstract. Advances in whole-genome sequencing (WGS) promise to enable the accurate and comprehensive structural variant (SV) discovery. Dissecting SVs from ...
People also ask
What is the best structural variant caller?
What is the analysis of WGS data?
Abstract. AbstractAdvances in whole-genome sequencing (WGS) promise to enable the accurate and comprehensive structural variant (SV) discovery. Dissecting SVs ...
Mar 28, 2024 · This study evaluated recently published and widely used SV callers with identified variants from a massive whole-genome sequencing (WGS) dataset ...