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Software

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IBM SPSS Statistics is a powerful statistical software platform. It offers a user-friendly interface and a robust set of features that lets your organization quickly extract actionable insights from your data. Advanced statistical procedures help ensure high accuracy and quality decision making. All facets of the analytics lifecycle are included, from data preparation and management to analysis and reporting.

Available Versions
Available Versions
Unspecified: 24

SQLite3 is an SQL database engine in a C library. Programs that link the SQLite3 library can have SQL database access without running a separate RDBMS process.

Available Versions
Available Versions
Bell: 3.30.1
Gilbreth: 3.30.1
Negishi: 3.39.4
Scholar: 3.30.1

SqueezeMeta is a fully automated metagenomics pipeline, from reads to bins.

Available Versions
Available Versions
Unspecified: 1.5.1

SQUID is designed to detect both fusion-gene and non-fusion-gene transcriptomic structural variations from RNA-seq alignment.

Available Versions
Available Versions
Unspecified: 1.5

The NCBI SRA Toolkit enables reading dumping of sequencing files from the SRA database and writing loading files into the .sra format.

Available Versions
Available Versions
Anvil: 2.10.9

SRA-Toolkit is a collection of tools and libraries for using data in the INSDC Sequence Read Archives

Available Versions
Available Versions
Unspecified: 2.11.0-pl5262

Srst2 is designed to take Illumina sequence data, a MLST database and/or a database of gene sequences (e.g. resistance genes, virulence genes, etc) and report the presence of STs and/or reference genes.

Available Versions
Available Versions
Unspecified: 0.2.0

Stacks is a software pipeline for building loci from RAD-seq.

Available Versions
Available Versions
Unspecified: 2.60

STAR: ultrafast universal RNA-seq aligner.

Available Versions
Available Versions
Unspecified: 2.7.10a 2.7.10b 2.7.9a

STAR-Fusion is a component of the Trinity Cancer Transcriptome Analysis Toolkit (CTAT).

Available Versions
Available Versions
Unspecified: 1.11b

staramr scans bacterial genome contigs against the ResFinder, PointFinder, and PlasmidFinder databases (used by the ResFinder webservice and other webservices offered by the Center for Genomic Epidemiology) and compiles a summary report of detected antimicrobial resistance genes.

Available Versions
Available Versions
Unspecified: 0.7.1

Stata is a complete, integrated software package that provides all your data science needs?data manipulation, visualization, statistics, and automated reporting.

Available Versions
Available Versions
Bell: 18
Gilbreth: 17
Scholar: 17

Stata/MP is the fastest and largest edition of Stata. Stata is a complete, integrated software package that provides all your data science needs?data manipulation, visualization, statistics, and automated reporting.

Available Versions
Available Versions
Bell: 17
Scholar: 17

STREAM (Single-cell Trajectories Reconstruction, Exploration And Mapping) is an interactive pipeline capable of disentangling and visualizing complex branching trajectories from both single-cell transcriptomic and epigenomic data.

Available Versions
Available Versions
Unspecified: 1.0

Stringdecomposer is a tool for decomposition centromeric assemblies and long reads into monomers.

Available Versions
Available Versions
Unspecified: 1.1.2

Stringtie employs efficient algorithms for transcript structure recovery and abundance estimation from bulk RNA-Seq reads aligned to a reference genome. It takes as input spliced alignments in coordinate-sorted SAM/BAM/CRAM format and produces a GTF output which consists of assembled transcript structures and their estimated expression levels (FPKM/TPM and base coverage values).

Available Versions
Available Versions
Unspecified: 2.1.7 2.2.1

STRique is a python package to analyze repeat expansion and methylation states of short tandem repeats (STR) in Oxford Nanopore Technology (ONT) long read sequencing data.

Available Versions
Available Versions
Unspecified: 0.4.2

Structure is a software package for using multi-locus genotype data to investigate population structure.

Available Versions
Available Versions
Unspecified: 2.3.4

Subread carries out high-performance read alignment, quantification and mutation discovery. It is a general-purpose read aligner which can be used to map both genomic DNA-seq reads and DNA-seq reads.

Available Versions
Available Versions
Unspecified: 1.6.4 2.0.1

Subversion is an open source version control system.

Available Versions
Available Versions
Gilbreth: Current
Scholar: Current