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Software

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Snap is a semi-HMM-based Nucleic Acid Parser -- gene prediction tool.

Available Versions
Available Versions
Unspecified: 2013_11_29

Snap-aligner (Scalable Nucleotide Alignment Program) is a fast and accurate read aligner for high-throughput sequencing data.

Available Versions
Available Versions
Unspecified: 2.0.0

Snaptools is a python module for pre-processing and working with snap file.

Available Versions
Available Versions
Unspecified: 1.4.8

Snippy is a tool for rapid haploid variant calling and core genome alignment.

Available Versions
Available Versions
Unspecified: 4.6.0

Snp-dists is a tool to convert a FASTA alignment to SNP distance matrix.

Available Versions
Available Versions
Unspecified: 0.8.2

SNP-sites is a tool that apidly extracts SNPs from a multi-FASTA alignment.

Available Versions
Available Versions
Unspecified: 2.5.1

Snpeff is an open source tool that annotates variants and predicts their effects on genes by using an interval forest approach.

Available Versions
Available Versions
Unspecified: 5.1 5.1d

Snpgenie is a collection of Perl scripts for estimating ?N/?S, dN/dS, and gene diversity from next-generation sequencing (NGS) single-nucleotide polymorphism (SNP) variant data.

Available Versions
Available Versions
Unspecified: 1.0

Snphylo is a pipeline to generate a phylogenetic tree from huge SNP data.

Available Versions
Available Versions
Unspecified: 20180901

Snpsift is a tool used to annotate genomic variants using databases, filters, and manipulates genomic annotated variants.

Available Versions
Available Versions
Unspecified: 4.3.1t

Soapdenovo2 is a short-read assembly method to build de novo draft assembly.

Available Versions
Available Versions
Unspecified: 2.40

SortMeRNA is a local sequence alignment tool for filtering, mapping and clustering.

Available Versions
Available Versions
Unspecified: 2.1b 4.3.4

souporcell is a method for clustering mixed-genotype scRNAseq experiments by individual.

Available Versions
Available Versions
Unspecified: 2.0

Sourmash is a tool for quickly search, compare, and analyze genomic and metagenomic data sets.

Available Versions
Available Versions
Unspecified: 4.3.0 4.5.0

Spaceranger is a set of analysis pipelines that process Visium Spatial Gene Expression data with brightfield and fluorescence microscope images.

Available Versions
Available Versions
Unspecified: 1.3.0 1.3.1 2.0.0

SPAdes - St. Petersburg genome assembler - is an assembly toolkit containing various assembly pipelines.

Available Versions
Available Versions
Unspecified: 3.15.3 3.15.4 3.15.5

Apache Spark is a fast and general engine for large-scale data processing.

Available Versions
Available Versions
Anvil: 3.1.1
Bell: 2.4.4
Gilbreth: 2.4.4
Negishi: 3.1.1
Scholar: 2.4.4

SPECFEM3D Cartesian simulates acoustic fluid, elastic solid, coupled acoustic/elastic, poroelastic or seismic wave propagation in any type of conforming mesh of hexahedra structured or not. It can, for instance, model seismic waves propagating in sedimentary basins or any other regional geological model following earthquakes. It can also be used for non-destructive testing or for ocean acoustics.

Available Versions
Available Versions
Bell: 20201122--h9c0626d1
Negishi: 20201122--h9c0626d1

SPECFEM3D Globe simulates global and regional continental-scale seismic wave propagation.

Available Versions
Available Versions
Bell: 20210322--h1ee10977
Negishi: 20210322--h1ee10977

Sprod: De-noising Spatially Resolved Transcriptomics Data Based on Position and Image Information.

Available Versions
Available Versions
Unspecified: 1.0