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https://www.agilent.com/en/product/cell-analysis/real-time-cell-metabolic-analysis/xf-software/seahorse-wave-controller-software-2-6-1-740904

Instrument control and data acquisition software for Agilent Seahorse XFe96 and XFe24 analyzers with Windows 10 64-bit OS only. Experiment design, instrument control, data analysis, and file management software. Software provides intuitive interface with predefined assay templates and streamlined experimental design for simplified metabolic analysis.

Proper citation: Agilent Seahorse Wave (RRID:SCR_024491) Copy   

•   Source: SciCrunch Registry
  

https://swissmodel.expasy.org/lddt

Web server for local superposition free score for comparing protein structures and models using distance difference tests. Superposition free score that evaluates local distance differences of all atoms in model, including validation of stereochemical plausibility.

Proper citation: lDDT (RRID:SCR_024524) Copy   

•   Source: SciCrunch Registry
  

https://github.com/adamallo/SimPhy

Software package for simulation of multiple gene families evolving under incomplete lineage sorting, gene duplication and loss, horizontal gene transfer, all three potentially leading to species tree/gene tree discordance and gene conversion. Used for phylogenomic simulation of gene, locus, and species trees.

Proper citation: SimPhy (RRID:SCR_024501) Copy   

•   Source: SciCrunch Registry
  

http://mutationassessor.org/r3/

Web server predicts functional impact of amino-acid substitutions in proteins, such as mutations discovered in cancer or missense polymorphisms. Functional impact is assessed based on evolutionary conservation of affected amino acid in protein homologs., THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025.

Proper citation: Mutation Assessor (RRID:SCR_024502) Copy   

•   Source: SciCrunch Registry
  

https://github.com/pinellolab/CRISPResso2

Software pipeline designed to enable rapid and intuitive interpretation of genome editing experiments. Used for analysis of deep sequencing data for rapid and intuitive interpretation of genome editing experiments.

Proper citation: CRISPResso2 (RRID:SCR_024503) Copy   

•   Source: SciCrunch Registry
  

https://silebat.github.io/FSK-Lab/openbugs.html

Software for analysing complex statistical models using Markov chain Monte Carlo methods.

Proper citation: OpenBUGS (RRID:SCR_024488) Copy   

•   Source: SciCrunch Registry
  

https://github.com/bzhanglab/AutoRT/

Software tool for peptide retention time prediction using deep learning. Supports peptide retention prediction for tryptic peptides, MHC bound peptides and PTM peptides.

Proper citation: AutoRT (RRID:SCR_024513) Copy   

•   Source: SciCrunch Registry
  

https://www.reading.ac.uk/bioinf/ModFOLD/

Web server for the global and local quality estimation of 3D protein models

Proper citation: ModFOLD (RRID:SCR_024518) Copy   

•   Source: SciCrunch Registry
  

http://metscape.ncibi.org

A software program that allows users to visualize and interpret human metabolim and expression profiling data by providing users with a bioinformatics framework. Its features include bulding and analyzing networks of genes and compounds, identifying enriched pathways from expression profiling data, and visualizing changes in metabolite data.

Proper citation: Metscape (RRID:SCR_014687) Copy   

•   Source: SciCrunch Registry
  

http://www.bic.mni.mcgill.ca/software/minc/

A medical imaging data format and an associated set of tools and libraries including a 3 level API for medical image analysis with a particular focus on the needs of research. There are also a number of tools including Registration and Non-Uniformity correction.

Proper citation: MINC (RRID:SCR_002391) Copy   

•   Source: SciCrunch Registry
  

https://github.com/Tarskin/LaCyTools

Software high throughput data extraction package for LC-MS data.Targeted Liquid Chromatography-Mass Spectrometry data processing package for relative quantitation of glycopeptides.

Proper citation: LaCyTools (RRID:SCR_024525) Copy   

•   Source: SciCrunch Registry
  

https://CRAN.R-project.org/package=GOplot

Software R package for visually combining expression data with functional analysis.

Proper citation: GOplot (RRID:SCR_024419) Copy   

•   Source: SciCrunch Registry
  

https://CRAN.R-project.org/package=geepack

Software R package implements generalized estimating equations for parameters in mean, scale, and correlation structures, through mean link, scale link, and correlation link. Can handle clustered categorical responses. Used for fitting marginal generalized linear models to clustered data.

Proper citation: geepack (RRID:SCR_024510) Copy   

•   Source: SciCrunch Registry
  

https://cran.r-project.org/web/packages/dagitty/

Software R package provides access to all of the capabilities of DAGitty web application for drawing and analysing Directed Acyclic Graphs within the R platform for statistical computing. Used for graphical analysis of structural causal models.

Proper citation: DAGitty (RRID:SCR_024509) Copy   

•   Source: SciCrunch Registry
  

https://github.com/ekmolloy/fastmulrfs

Software pipeline for estimating species trees from multi copy gene trees.

Proper citation: FastMulRFS (RRID:SCR_024505) Copy   

•   Source: SciCrunch Registry
  

http://www.cs.cmu.edu/~durand/Notung/

Software package to facilitate large scale analysis, using both rooted and unrooted trees.Used for dating gene duplications and optimizing gene family trees.Used for inferring duplication dates from gene trees automatically and can also be used as exploratory analysis tool for evaluating alternative hypotheses.

Proper citation: NOTUNG (RRID:SCR_024484) Copy   

•   Source: SciCrunch Registry
  

https://CRAN.R-project.org/package=CMplot

Software drawing R package designed for Manhattan plot of genomic analysis.

Proper citation: CMplot (RRID:SCR_024514) Copy   

•   Source: SciCrunch Registry
  

https://github.com/PoisonAlien/Maftools

Software R package offers multitude of analysis and visualization modules that are commonly used in cancer genomic studies, including driver gene identification, pathway, signature, enrichment, and association analyses. Maftools requires somatic variants in Mutation Annotation Format (MAF) and is independent of larger alignment files.

Proper citation: maftools (RRID:SCR_024519) Copy   

•   Source: SciCrunch Registry
  

http://srv00.recas.ba.infn.it/ASPicDB/

A database to access reliable annotations of the alternative splicing pattern of human genes, obtained by ASPic algorithm (Castrignano et al. 2006), and to the functional annotation of predicted isoforms. Users may select and extract specific sets of data related to genes, transcripts and introns fulfilling a combination of user-defined criteria. Several tabular and graphical views of the results are presented, providing a comprehensive assessment of the functional implication of alternative splicing in the gene set under investigation. ASPicDB also includes information on tissue-specific splicing patterns of normal and cancer cells, based on available EST data and their library source annotation.

Proper citation: ASPicDB (RRID:SCR_002102) Copy   

•   Source: SciCrunch Registry
  

http://tcoffee.crg.cat/apps/tcoffee/do:regular

A multiple sequence alignment server which can align Protein, DNA and RNA sequences.

Proper citation: T-Coffee (RRID:SCR_011818) Copy   

•   Source: SciCrunch Registry