iCallSV is a Python library and command-line software toolkit to call structural aberrations from Next Generation DNA sequencing data. Behind the scenes it uses Delly2 to do structural variant calling. It is designed for use with hybrid capture, including both whole-exome and custom target panels, and short-read sequencing platforms such as Illumina
<div><p>Existing methods for identifying structural variants (SVs) from short read datasets are inac...
Background: Structural variations (SVs), such as insertions, deletions, inversions, and duplications...
Structural variations (SV) are broadly defined as genomic alterations that affect >50 bp of DNA, whi...
iAnnotateSV is a Python library and command-line software toolkit to annotate and visualize structur...
Variant discovery in medical research typically involves alignment of short sequencing reads to the ...
<div><p></p><p>Next-generation sequencing technologies expedited research to develop efficient compu...
Motivation: Despite widespread prevalence of somatic structural variations (SVs) across most tumor t...
Structural variant (SV) differences between human genomes can cause germline and mosaic disease as w...
Next-generation sequencing technologies expedited research to develop efficient computational tools ...
MutantHuntWGS is a user-friendly pipeline for analyzing Saccharomyces cerevisiae whole-genome sequen...
With the dramatic increase of pangenomic analysis, Human geneticists have generated large amount of ...
The incomplete identification of structural variants (SVs) from whole-genome sequencing data limits ...
Discovery of copy number variations (CNVs), a major category of structural variations, have dramatic...
The incomplete identification of structural variants (SVs) from whole-genome sequencing data limits ...
The accurate detection of bona fide causal DNA mutations in a sequenced sample is critical for gene ...
<div><p>Existing methods for identifying structural variants (SVs) from short read datasets are inac...
Background: Structural variations (SVs), such as insertions, deletions, inversions, and duplications...
Structural variations (SV) are broadly defined as genomic alterations that affect >50 bp of DNA, whi...
iAnnotateSV is a Python library and command-line software toolkit to annotate and visualize structur...
Variant discovery in medical research typically involves alignment of short sequencing reads to the ...
<div><p></p><p>Next-generation sequencing technologies expedited research to develop efficient compu...
Motivation: Despite widespread prevalence of somatic structural variations (SVs) across most tumor t...
Structural variant (SV) differences between human genomes can cause germline and mosaic disease as w...
Next-generation sequencing technologies expedited research to develop efficient computational tools ...
MutantHuntWGS is a user-friendly pipeline for analyzing Saccharomyces cerevisiae whole-genome sequen...
With the dramatic increase of pangenomic analysis, Human geneticists have generated large amount of ...
The incomplete identification of structural variants (SVs) from whole-genome sequencing data limits ...
Discovery of copy number variations (CNVs), a major category of structural variations, have dramatic...
The incomplete identification of structural variants (SVs) from whole-genome sequencing data limits ...
The accurate detection of bona fide causal DNA mutations in a sequenced sample is critical for gene ...
<div><p>Existing methods for identifying structural variants (SVs) from short read datasets are inac...
Background: Structural variations (SVs), such as insertions, deletions, inversions, and duplications...
Structural variations (SV) are broadly defined as genomic alterations that affect >50 bp of DNA, whi...