cutesv
comprehensive discovery of structural variations of genomic sequences
Command lineScience
Not tested on a device yet. What that means
Commands in the package
cuteSV
About cutesv
From Debian's package description
Long-read sequencing enables the comprehensive discovery of structural variations (SVs). However, it is still non-trivial to achieve high sensitivity and performance simultaneously due to the complex SV characteristics implied by noisy long reads.
cuteSV is a sensitive, fast and scalable long-read-based SV detection approach. cuteSV uses tailored methods to collect the signatures of various types of SVs and employs a clustering-and-refinement method to analyze the signatures to implement sensitive SV detection. Benchmarks on real Pacific Biosciences (PacBio) and Oxford Nanopore Technology (ONT) datasets demonstrate that cuteSV has better yields and scalability than state-of-the-art tools.
From Debian's description of the cutesv package, under that package's license.
Dependencies
Depends on
python3-biopythonpython3-cigarpython3-numpypython3-pysampython3-scipypython3-sklearnpython3python3-vcf
Related apps
- FastQC quality controlquality control for high throughput sequence data
- minimap2versatile pairwise aligner for genomic and spliced nucleotide sequencesCommand line
- bbmapBBTools genomic aligner and other tools for short sequencesCommand line
- seergenomic sequence element (kmer) enrichment analysisCommand line
- optimirIntegrating genetic variations in miRNA alignmentCommand line
- kmamapping genomic sequences to raw reads directly against redundant databasesCommand line
Sources and licenses
- Name: the Debian package name.
- Summary: Debian's short description of the cutesv package, under that package's license.
- Description: Debian's description of the cutesv package, under that package's license.
- Versions and sizes: Debian's archive for ARM64, as on packages.debian.org.
- Popularity: Debian Popularity Contest counts.
More in About the catalog.