Tools   Select Another Resource Report Type

https://github.com/galaxyproject/tools-iuc/tree/master/tools/scater

Software tool as Galaxy based training resource for single cell RNA-seq quality control and analyses.

Proper citation: Galaxy scater (RRID:SCR_017394) Copy   

•   Source: SciCrunch Registry

http://heimanlab.com/cut2.html

Software tool to find restriction endonucleases. Helps restriction map nucleotide sequences. Tool with customizable interface, platform independent accessibility, interfaces to NCBI's GenBank, DNA sequence database, and NEB's REBase, and restriction enzyme database. In addition to restriction site mapping, Webcutter 2 also performs degenerate digests, including option of finding restriction sites that can be introduced into sequence by silent mutagenesis.

Proper citation: Webcutter (RRID:SCR_017638) Copy   

•   Source: SciCrunch Registry

https://www.synapse.org/#!Synapse:syn11459638

Dockerized environment for winning algorithm in 2017 Multiple Myeloma DREAM Challenge, Sub-Challenge 3.

Proper citation: Multiple Myeloma survival predictor (RRID:SCR_017651) Copy   

•   Source: SciCrunch Registry

http://genelab.nasa.gov

Omics database for spaceflight experiments. Interactive, open access resource where scientists can upload, download, store, search, share, transfer, and analyze omics data from spaceflight and corresponding analogue experiments. Enables exploration of molecular network responses of terrestrial biology to space environment. Contains curated omics data, metadata and radiation dosimetry for model organisms. Supports standard guidelines for submission of datasets, MIAME for microarray, ENCODE Consortium Guidelines for RNA-seq and MIAPE Guidelines for proteomics.

Proper citation: GeneLab (RRID:SCR_017658) Copy   

•   Source: SciCrunch Registry

https://github.com/tanghaibao/mcscan

Software package to simultaneously scan multiple genomes to identify homologous chromosomal regions and subsequently align these regions using genes as anchors.Used to identify conserved gene arrays both within same genome and across different genomes. Command line program to wrap dagchainer and combine pairwise results into multi alignments in column format.

Proper citation: MCScan (RRID:SCR_017650) Copy   

•   Source: SciCrunch Registry

https://discover.blackfynn.com/

THIS RESOURCE IS NO LONGER IN SERVICE. Documented on February 22, 2023. Data repository for scientific data. Open data library to explore neuroscience data for neurodegenerative diseases for which there are no disease modifying treatments.

Proper citation: Blackfynn Discover (RRID:SCR_018068) Copy   

•   Source: SciCrunch Registry

https://blobtools.readme.io/docs

Software tool as modular command line solution for visualisation, quality control and taxonomic partitioning of genome datasets. Used for interrogation of genome assemblies. Assists in primary partitioning of data, leading to improved assemblies, and screening of final assemblies for potential contaminants.

Proper citation: Blobtools (RRID:SCR_017618) Copy   

•   Source: SciCrunch Registry

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

Software tool for applying user guided nonlinear refinements (inplane) to existing, affine 2D-to-3D registration. Used for precise quantitative analysis of residual anatomical variability among test subjects after registration with QuickNII. VisuAlign is part of the QUINT workflow.

Proper citation: VisuAlign (RRID:SCR_017978) Copy   

•   Source: SciCrunch Registry

https://haddock.science.uu.nl/dna/dna.php

DNA structure modelling server. Web server for generating custom 3D structural models of DNA with control over local and global conformation.

Proper citation: 3D DART (RRID:SCR_017588) Copy   

•   Source: SciCrunch Registry

https://github.com/philres/ngmlr

Software tool as long read mapper designed to align PacBio or Oxford Nanopore reads to reference genome and optimized for structural variation detection.

Proper citation: Ngmlr (RRID:SCR_017620) Copy   

•   Source: SciCrunch Registry

https://bioinfo3d.cs.tau.ac.il/PatchDock/

Web server for molecular docking. Performs structure prediction of protein–protein and protein–small molecule complexes. Molecular docking algorithm based on shape complementarity principles.

Proper citation: PatchDock (RRID:SCR_017589) Copy   

•   Source: SciCrunch Registry

https://rayyan.qcri.org/welcome

Software tool for screening papers for systematic reviews. Web and mobile app to help to expedite initial screening of abstracts and titles using process of semi automation while incorporating high level of usability.

Proper citation: Rayyan QCRI (RRID:SCR_017584) Copy   

•   Source: SciCrunch Registry

http://neurocics.udd.cl/LANtoolbox.html

Software toolbox for neuroscientist data (EEG and reaction time for time being). Used to create shared language among different algorithms and softwares in this field (e.g. Fieldtrip, Eeglab, Chronux, Brainstorm, etc), in order to facilitate implementation of experimental analysis by users. Code and scripts for EEG analysis for MATLAB.

Proper citation: LAN toolbox (RRID:SCR_017629) Copy   

•   Source: SciCrunch Registry

https://www.mq.edu.au/

Public research university based in Sydney, Australia, in suburb of Macquarie Park. Founded in 1964 by New South Wales Government, it was third university to be established in metropolitan area of Sydney.

Proper citation: Macquarie University; Sydney; Australia (RRID:SCR_017596) Copy   

•   Source: SciCrunch Registry

http://www.touptek.com/product/showproduct.php?id=103&lang=en

Software tool that controls microscope camera by Touptek Photomics. Provides functions to fully control camera and present video stream processed by Ultra FineTM color engine at high speed, which includes dedicated pipeline to process raw data into realistic scene. Compatible with ToupCam full series of digital cameras. With authorized license, ToupView software could be used with other cameras which support Twain or DirectShow interface. Used in field of medical microscopic imaging, industrial detection, machine vision, astronomical observation, etc.

Proper citation: ToupView (RRID:SCR_017998) Copy   

•   Source: SciCrunch Registry

https://www.bioassayexpress.com/

Web based tool for annotating bioassay protocols using semantic web terms. Enables searching, sorting, clustering and analyzing of assays without needing to read through original text. Exploits Common Assay Template based on underlying vocabularies and semantic standards from BioAssay Ontology, Drug Target Ontology, Cell Line Ontology and others. Users can identify similar assays and examine similarity of assays between and within organizations.

Proper citation: BioAssay Express (RRID:SCR_017594) Copy   

•   Source: SciCrunch Registry

https://www.biotite-python.org/

Software Python package bundling popular tasks in computational molecular biology, from sequence analysis to structural bioinformatics. Comprehensive library for computational molecular biology. Package features sequence and structure data analysis and editing functionality, support for common sequence and structure file formats, visualization capabilities, interfaces to external software (MSA software, BLAST, DSSP). Operating system(s): Windows, OS X, Linux.

Proper citation: Biotite (RRID:SCR_017593) Copy   

•   Source: SciCrunch Registry

https://github.com/WangHYLab/fcirc

Software Python pipeline for linear and circular RNAs of known fusions exploration. Pipeline for exploring linear transcripts and circRNAs of known fusions based on RNA-Seq data. Known fusion genes are from multiple databases like COSMIC, ChimerDB, TicDB, FARE-CAFE and FusionCancer or user-added gene-pairs.

Proper citation: Fcirc (RRID:SCR_018090) Copy   

•   Source: SciCrunch Registry

http://www.syglass.io

Software visualization tool for direct volume rendering with no segmentation required. Enables users to view, annotate and analyze 3D data in VR. Data visualization and annotation system that allows rendering of large, volumetric data in its true, three- or four-dimensional form.

Proper citation: syGlass (RRID:SCR_017961) Copy   

•   Source: SciCrunch Registry

https://portal.brain-map.org/atlases-and-data/rnaseq

Software tool to visualize and analyze transcriptomics data and transcriptomic cell types for mouse and human, all directly in web browser. To explore gene expression heatmap across cell types in datasets, search for genes of interest, explore tSNE visualization, colored by cell types or expression of genes of interest, visualize dataset’s sampling strategy to see how cells and nuclei were sampled across brain areas, cortical layer, and other dimensions, find cell type of interest in one visualization and see its characteristics in different visualization.Used for Allen Brain Map Cell Types Database to Browse Data: Human - Multiple Cortical Areas, and Mouse - Cortex and Hippocampus.

Proper citation: Transcriptomics Explorer (RRID:SCR_017567) Copy   

•   Source: SciCrunch Registry