Tools   Select Another Resource Report Type

https://github.com/GATB/MindTheGap

Software tool to perform detection and assembly of DNA insertion variants in NGS read datasets with respect to reference genome.Used to call insertions of any size, whether they are novel or duplicated, homozygous or heterozygous in the donor genome.

Proper citation: MindTheGap (RRID:SCR_024115) Copy   

•   Source: SciCrunch Registry

https://jydu.github.io/maffilter/

Software tool for analysis of genome alignments. It parses and manipulates MAF files as well as more simple fasta files. Despite various filtering options and format conversion tools, MafFilter can compute a wide range of statistics including phylogenetic trees, nucleotide diversity, inferrence of selection, etc.

Proper citation: MafFilter (RRID:SCR_024105) Copy   

•   Source: SciCrunch Registry

http://maude.cs.illinois.edu/w/index.php/The_Maude_System

Software high performance reflective language and system supporting both equational and rewriting logic specification and programming for wide range of applications.Supports equational specification and programming, rewriting logic computation.

Proper citation: Maude (RRID:SCR_024108) Copy   

•   Source: SciCrunch Registry

https://github.com/Pas-Kapli/mptp

Software tool for single locus species delimitation. Implements fast method to compute the ML delimitation from inferred phylogenetic tree of the samples.Used to handle very large biodiversity datasets.

Proper citation: mPTP (RRID:SCR_024121) Copy   

•   Source: SciCrunch Registry

http://ugovaretto.github.io/molekel/

Open source multi platform molecular visualization program.

Proper citation: Molekel (RRID:SCR_024122) Copy   

•   Source: SciCrunch Registry

https://www.mrtrix.org/

Software tools to perform various types of diffusion MRI analyses, from various forms of tractography through to next-generation group-level analyses.

Proper citation: MRtrix3 (RRID:SCR_024123) Copy   

•   Source: SciCrunch Registry

http://www.ctsim.org

Software tool to simulate process of transmitting X-rays through phantom objects. Reconstructs original phantom image from projections. Has wide array of image analysis and image processing functions.

Proper citation: CTSim (RRID:SCR_024004) Copy   

•   Source: SciCrunch Registry

https://www.imsc.res.in/~rsidd/sigma/

Software alignment program with new algorithm and scoring scheme designed specifically for non-coding DNA sequence. This problem is now growing in importance with the increasing number of fully-sequenced species. In particular, studies of gene regulation seek to take advantage of comparative genomics, and recent algorithms (such as PhyloGibbs) for finding regulatory sites in phylogenetically-related intergenic sequence require alignment as a preprocessing step.

Proper citation: sigma-align (RRID:SCR_024337) Copy   

•   Source: SciCrunch Registry

https://github.com/ArtRand/signalAlign

Software tool to align ionic current from MinION to reference sequence using trainable hidden Markov model. HMM-HDP models for MinION signal alignments,

Proper citation: signalalign (RRID:SCR_024339) Copy   

•   Source: SciCrunch Registry

https://github.com/babinyurii/recan

Software tool as genetic distance plotting for recombination events analysis.

Proper citation: recan (RRID:SCR_024317) Copy   

•   Source: SciCrunch Registry

https://github.com/bioinfo-center-pasteur-fr/toppred

Software tool for membrane protein structure prediction.Transmembrane topology prediction.Used for predicting topology of bacterial inner membrane proteins.

Proper citation: toppred (RRID:SCR_024385) Copy   

•   Source: SciCrunch Registry

https://github.com/sina-cb/Tn-seqExplorer

Software package written in Java for analysis of high-throughput sequencing data of transposon mutant libraries.Reads the alignment and the gene annotation, and provides the user with set of tools to investigate data and identify possibly essential or advantageous genes as those that contain significantly low counts of transposon insertions.

Proper citation: Tn-seq explorer (RRID:SCR_024387) Copy   

•   Source: SciCrunch Registry

http://saclab.tamu.edu/essentiality/transit/

Software tool for Himar1 TnSeq analysis.Provides graphical interface to three different statistical methods for analyzing TnSeq data. Used for identifying essential genes in individual datasets as well as comparative analysis between conditions.

Proper citation: TRANSIT (RRID:SCR_024389) Copy   

•   Source: SciCrunch Registry

http://www.tree-puzzle.de

Software tool to reconstruct phylogenetic trees from molecular sequence data by maximum likelihood. Allows analysis of large data sets and automatically assigns estimations of support to each internal branch. Computes pairwise maximum likelihood distances as well as branch lengths for user specified trees.Conducts statistical tests on the data set.

Proper citation: TREE-PUZZLE (RRID:SCR_024382) Copy   

•   Source: SciCrunch Registry

https://qtlreaper.sourceforge.net/

Software, written in C and compiled as Python module, for rapidly scanning microarray expression data for Quantitative Trait Locies. Searches for association between each expression trait and all genotypes and evaluates that association by permutation test. Performs bootstrap resampling to estimate confidence region for location of putative QTL.

Proper citation: qtlreaper (RRID:SCR_024199) Copy   

•   Source: SciCrunch Registry

https://sparta.readthedocs.io/en/latest/

Software workflow aimed at analyzing single-end Illumina RNA-seq data. The software is supported on Windows, Mac OS X, and Linux platforms.

Proper citation: sparta (RRID:SCR_024349) Copy   

•   Source: SciCrunch Registry

https://github.com/bartongroup/yanosim

Software tool as read simulator for nanopore DRS datasets.

Proper citation: Yanosim (RRID:SCR_024363) Copy   

•   Source: SciCrunch Registry

https://cab.spbu.ru/software/spades/

Software package for assembling single cell genomes and mini metagenomes. Uses short read sets as input. Used for genomes of uncultivatable bacteria that vastly exceeds what may be obtained via traditional metagenomics studies. Works with Illumina or IonTorrent reads and can provide hybrid assemblies using PacBio, Oxford Nanopore and Sanger reads. Intended for small genomes like bacterial or fungal., THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025.

Proper citation: SPAdes (RRID:SCR_000131) Copy   

•   Source: SciCrunch Registry

http://sourceforge.net/projects/skewer/

Software program for adapter trimming that is specially designed for processing Illumina paired-end sequences.

Proper citation: skewer (RRID:SCR_001151) Copy   

•   Source: SciCrunch Registry

https://github.com/princelab/mspire-simulator

A free, open-source shotgun proteomic simulator that goes beyond previous simulation attempts by generating LC-MS features with realistic m/z and intensity variance along with other noise components.

Proper citation: Mspire-Simulator (RRID:SCR_001431) Copy   

•   Source: SciCrunch Registry