Structural Variants (SVs) are genomic rearrangements of more than 50 base pairs. Since SVs can reach several thousand base pairs, they can have huge impacts on genome functions, studying SVs is, therefore, of great interest. Recently, a new generation of sequencing technologies has been developed and produce long read data of tens of thousand of base pairs which are particularly useful for spanning over SV breakpoints. So far, bioinformatics methods have focused on the SV discovery problem with long read data. However, no method has been proposed to specifically address the issue of genotyping SVs with long read data. The purpose of SV genotyping is to assess for each variant of a given input set which alleles are present in a newly sequenc...
Next-generation sequencing technologies expedited research to develop efficient computational tools ...
The incomplete identification of structural variants (SVs) from whole-genome sequencing data limits ...
An increasingly important scenario in population genetics is when a large cohort has been genotyped ...
Structural Variants (SVs) are genomic rearrangements of more than 50 base pairs. Since SVs can reach...
Structural Variants (SVs) are genomic rearrangements of more than 50 base pairs. Since SVs can reach...
International audienceMotivation: Studies on structural variants (SV) are expanding rapidly. As a re...
International audienceStructural variants (SVs) are genomic segments of more than 50 bp that have be...
International audienceStructural variants (SVs) are genomic segments of more than 50 bp that have be...
Structural variants (SVs) account for a large amount of sequence variability across genomes and play...
Abstract Background With the rapid development of long-read sequencing technologies, it is possible ...
Although various methods have been developed to detect structural variations (SVs) in genomic sequen...
DNA sequencing has become a ubiquitous part of individualized medicine, playing central roles in the...
Motivation: Structural variants are defined as genomic variants larger than 50bp. They have been sho...
Structural variants (SVs) and short tandem repeats (STRs) are important sources of genetic diversity...
Recent advances in long-read sequencing have given us an unprecedented view of structural variants (...
Next-generation sequencing technologies expedited research to develop efficient computational tools ...
The incomplete identification of structural variants (SVs) from whole-genome sequencing data limits ...
An increasingly important scenario in population genetics is when a large cohort has been genotyped ...
Structural Variants (SVs) are genomic rearrangements of more than 50 base pairs. Since SVs can reach...
Structural Variants (SVs) are genomic rearrangements of more than 50 base pairs. Since SVs can reach...
International audienceMotivation: Studies on structural variants (SV) are expanding rapidly. As a re...
International audienceStructural variants (SVs) are genomic segments of more than 50 bp that have be...
International audienceStructural variants (SVs) are genomic segments of more than 50 bp that have be...
Structural variants (SVs) account for a large amount of sequence variability across genomes and play...
Abstract Background With the rapid development of long-read sequencing technologies, it is possible ...
Although various methods have been developed to detect structural variations (SVs) in genomic sequen...
DNA sequencing has become a ubiquitous part of individualized medicine, playing central roles in the...
Motivation: Structural variants are defined as genomic variants larger than 50bp. They have been sho...
Structural variants (SVs) and short tandem repeats (STRs) are important sources of genetic diversity...
Recent advances in long-read sequencing have given us an unprecedented view of structural variants (...
Next-generation sequencing technologies expedited research to develop efficient computational tools ...
The incomplete identification of structural variants (SVs) from whole-genome sequencing data limits ...
An increasingly important scenario in population genetics is when a large cohort has been genotyped ...