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http://gmt.genome.wustl.edu/pindel/0.2.4/

Software to detect breakpoints of large deletions, medium sized insertions, inversions, tandem duplications and other structural variants at single-based resolution from next-gen sequence data. It uses a pattern growth approach to identify the breakpoints of these variants from paired-end short reads., THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025.

Proper citation: Pindel (RRID:SCR_000560) Copy   

•   Source: SciCrunch Registry
  

http://code.google.com/p/ontomorphtab/

OntoMorph is a tab plugin for Protege-OWL 3 that allows a user to mark-up portions of a Neurolucida neuron morphology with OWL instances. A user loads a Neurolucida morphology file, either from their hard drive or from an arbitrary URL, into an interface that allows them to zoom, rotate, and translate the morphology. The interface allows them to select points on the morphology to indicate points, segments, or subtrees of the morphology they wish to assign to an OWL instance. After this selection has been made, OntoMorph saves the selection to the currently active OWL instance in the ontology that is currently loaded into Protege. No modifications are made to the Neurolucida file itself. As a result, an association is created between that portion of the morphology and the OWL instance, such that selecting the OWL instance allows retrieval of the portion. Upon retrieval, the morphology portion can be highlighted, so the user can keep track of what pieces each instance refer to.

Proper citation: OntoMorph Tab (RRID:SCR_000443) Copy   

•   Source: SciCrunch Registry
  

http://www.broadinstitute.org/genome_bio/siphy/

Software that implements rigorous statistical tests to detect bases under selection from a multiple alignment data. It takes full advantage of deeply sequenced phylogenies to estimate both unlikely substitution patterns as well as slowdowns or accelerations in mutation rates. It can be applied as an Hidden Markov Model (HMM), in sliding windows, or to specific regions.

Proper citation: SiPhy (RRID:SCR_000564) Copy   

•   Source: SciCrunch Registry
  

https://github.com/NetherlandsMetabolomicsCentre/TNO-DECO

Matlab code for preprocessing gas chromatography mass spectrometry data.

Proper citation: TNO-DECO (RRID:SCR_000440) Copy   

•   Source: SciCrunch Registry
  

http://edwards.sdsu.edu/scaffold_builder/

THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 6,2023. Tool designed to generate scaffolds (super contigs of sequences joined by N-bases) using the homology provided by a closely related reference sequence. Scaffold_builder is an advanced wrapper for Nucmer, written in Python that resolves several situations that may arise when mapping contigs to the reference genome.

Proper citation: Scaffold builder (RRID:SCR_000556) Copy   

•   Source: SciCrunch Registry
  

http://lilab.stanford.edu/SNPiR/

Software for reliable Identification of Genomic Variants Using RNA-seq Data.

Proper citation: SNPiR (RRID:SCR_000557) Copy   

•   Source: SciCrunch Registry
  

http://paleogenomics.irmacs.sfu.ca/FPSAC/

Sogftware for fast Phylogenetic Scaffolding of Ancient Contigs.

Proper citation: FPSAC (RRID:SCR_000555) Copy   

•   Source: SciCrunch Registry
  

https://github.com/mickaelleclercq/mirdup

A software used for the validation of pre-miRNAs predictions as well as predict the final structure of mature miRNA.

Proper citation: MiRdup (RRID:SCR_000316) Copy   

•   Source: SciCrunch Registry
  

http://bbc.mdc-berlin.de/software

Multi-purpose SNV calling software enhanced by probabilistic integration of quality scores.

Proper citation: ACCUSA2 (RRID:SCR_000558) Copy   

•   Source: SciCrunch Registry
  

http://purl.bioontology.org/ontology/TEO

Ontology for representing events, time, and their relationships.

Proper citation: Time Event Ontology (RRID:SCR_000310) Copy   

•   Source: SciCrunch Registry
  

http://purl.bioontology.org/ontology/VARIO

An ontology for standardized, systematic description of effects, consequences and mechanisms of variations.

Proper citation: Variation Ontology (RRID:SCR_000311) Copy   

•   Source: SciCrunch Registry
  

https://posit.co/

Open source and enterprise ready professional software for R statistical computing environment. Integrated development environment for R. Includes console, syntax highlighting editor that supports direct code execution, as well as tools for plotting, history, debugging and workspace management. Available in open source and commercial editions and runs on desktop Windows, Mac, and Linux or in browser connected to RStudio Server or RStudio Server Pro (Debian/Ubuntu, RedHat/CentOS, and SUSE Linux).

Proper citation: RStudio (RRID:SCR_000432) Copy   

•   Source: SciCrunch Registry
  

https://code.google.com/p/dysc/

Software for Greedy Clustering of 16S rRNA Reads which uses a dynamic seeding strategy.

Proper citation: DySC (RRID:SCR_000553) Copy   

•   Source: SciCrunch Registry
  

http://purl.bioontology.org/ontology/SEDI

An ontology for DICOM as used in the SeDI project.

Proper citation: Semantic DICOM Ontology (RRID:SCR_000309) Copy   

•   Source: SciCrunch Registry
  

https://nei.nih.gov/health/clinicalstudies/

An archived portal of clinical studies, both ongoing and completed, that have been conducted and supported by the National Eye Institute (NEI) since 1970. The portal covers corneal diseases, glaucoma, epidemiology, lens and cataract, retinal diseases, strabismus, amblyopia and visual processing.

Proper citation: NEI Clinical Studies (RRID:SCR_000546) Copy   

•   Source: SciCrunch Registry
  

http://www.nitrc.org/projects/scribe/

Scribe encodes papers to populate the BrainMap Database

Proper citation: Scribe (RRID:SCR_000423) Copy   

•   Source: SciCrunch Registry
  

http://graphpad.com/

A commercial graphing software company that offers scientific software for statistical analyses, curve fitting and data analysis. It offers four programs: Prism, InStat, StatMate and QuickCalcs.

Proper citation: GraphPad (RRID:SCR_000306) Copy   

•   Source: SciCrunch Registry
  

http://www.altmetric.com/bookmarklet.php

Free bookmarklet for Chrome, Firefox and Safari that allows you to instantly get article level metrics for any recent paper. Simply drag the button below to your bookmarks bar, navigate to a journal article page, and hit Altmetric it!

Proper citation: Altmetric Bookmarklet (RRID:SCR_000427) Copy   

•   Source: SciCrunch Registry
  

http://wustl.edu/

Private research university in Greater St. Louis with its main campus mostly in unincorporated St. Louis County, Missouri and Clayton, Missouri.

Proper citation: Washington University in St. Louis; Missouri; USA (RRID:SCR_000343) Copy   

•   Source: SciCrunch Registry
  

https://sourceforge.net/projects/popbam/

A tool to perform evolutionary or population-based analyses of next-generation sequencing data. POPBAM takes a BAM file as its input and can compute many widely used evolutionary genetics measures in sliding windows across a genome.

Proper citation: POPBAM (RRID:SCR_000464) Copy   

•   Source: SciCrunch Registry