Searching the RRID Resource Information Network

Our searching services are busy right now. Please try again later

  • Register
X
Forgot Password

If you have forgotten your password you can enter your email here and get a temporary password sent to your email.

X

Leaving Community

Are you sure you want to leave this community? Leaving the community will revoke any permissions you have been granted in this community.

No
Yes
X
Forgot Password

If you have forgotten your password you can enter your email here and get a temporary password sent to your email.

SciCrunch Registry is a curated repository of scientific resources, with a focus on biomedical resources, including tools, databases, and core facilities - visit SciCrunch to register your resource.

Search

Type in a keyword to search

On page 21 showing 401 ~ 420 out of 1,647 results
Snippet view Table view Download Top 1000 Results
Click the to add this resource to a Collection
  • RRID:SCR_011919

    This resource has 1000+ mentions.

http://genome.ucsc.edu/cgi-bin/hgBlat?command=start

Software designed to quickly find sequences of 95% and greater similarity of length 25 bases or more.

Proper citation: BLAT (RRID:SCR_011919) Copy   


  • RRID:SCR_011877

    This resource has 1+ mentions.

http://www.bios.unc.edu/research/genomic_software/BBSeq/

A Powerful and Flexible Approach to the Analysis of RNA Sequence Count Data.

Proper citation: BBSeq (RRID:SCR_011877) Copy   


  • RRID:SCR_011893

    This resource has 10+ mentions.

http://kissplice.prabi.fr/

Software tool that enables analysis of RNA-seq data with or without reference genome. Local transcriptome assembler for SNPs, indels and AS events.

Proper citation: KisSplice (RRID:SCR_011893) Copy   


  • RRID:SCR_011851

    This resource has 100+ mentions.

http://uc-echo.sourceforge.net/

Error correction algorithm designed for short-reads from next-generation sequencing platforms such as Illumina''s Genome Analyzer II.

Proper citation: ECHO (RRID:SCR_011851) Copy   


  • RRID:SCR_011906

    This resource has 10+ mentions.

http://bioinformatics.mdanderson.org/main/PRADA:Overview

A pipeline to analyze paired end RNA-Seq data to generate gene expression values (RPKM) and gene-fusion candidates.

Proper citation: PRADA (RRID:SCR_011906) Copy   


  • RRID:SCR_011907

    This resource has 1+ mentions.

https://mcdonaldlab.biology.gatech.edu/r-sap/

An automated bioinformatics pipeline that analyzes and quantitates high-throughput RNA-Seq datasets.

Proper citation: R-SAP (RRID:SCR_011907) Copy   


  • RRID:SCR_011954

    This resource has 1+ mentions.

http://www.jiffynet.org/

Web based instant protein network modeler for newly sequenced species. Web server designed to instantly construct genome scale protein networks using protein sequence data. Provides network visualization, analysis pages and solution for instant network modeling of newly sequenced species.

Proper citation: JiffyNet (RRID:SCR_011954) Copy   


  • RRID:SCR_011955

    This resource has 1+ mentions.

http://www.optimaldesign.com/ArrayMiner/ArrayMiner.htm

A set of analysis tools using advanced algorithms to reveal the true structure of your gene expression data.

Proper citation: ArrayMiner (RRID:SCR_011955) Copy   


  • RRID:SCR_012105

    This resource has 10+ mentions.

http://sourceforge.net/projects/mirplant/

A user-friendly plant miRNA prediction tool.

Proper citation: miRPlant (RRID:SCR_012105) Copy   


  • RRID:SCR_012079

https://code.google.com/p/slidesort-bpr/

Software using a reference-free method for detecting clusters of breakpoints from the chromosomal rearrangements.

Proper citation: SlideSort-BPR (RRID:SCR_012079) Copy   


  • RRID:SCR_012002

    This resource has 10+ mentions.

http://www.bioinf.jku.at/software/fabia/fabia.html

A model-based technique for biclustering that is clustering rows and columns simultaneously.

Proper citation: FABIA (RRID:SCR_012002) Copy   


  • RRID:SCR_012049

    This resource has 10+ mentions.

http://mfpaq.sourceforge.net/

Software that allows fast and user-friendly verification of Mascot result files, as well as data quantification using isotopic labeling methods (SILAC/ICAT) or label free approaches (spectral counting, MS signal comparison).

Proper citation: MFPaQ (RRID:SCR_012049) Copy   


  • RRID:SCR_012058

    This resource has 1+ mentions.

http://sourceforge.net/projects/multiplierz/

An open-source Python-based environment that provides a scriptable framework for efficient access to manufacturers'' proprietary data files via mzAPI.

Proper citation: multiplierz (RRID:SCR_012058) Copy   


  • RRID:SCR_012029

    This resource has 1+ mentions.

http://www.computationalbioenergy.org/meta-storms.html

Optimized GPU-based software to efficiently measure the quantitative phylogenetic similarity among massive amount of microbial community samples.

Proper citation: GPU-Meta-Storms (RRID:SCR_012029) Copy   


  • RRID:SCR_012096

    This resource has 100+ mentions.

http://opencobra.sourceforge.net/openCOBRA/Welcome.html

Software Python package that provides support for basic COnstraint-Based Reconstruction and Analysis (COBRA) methods.

Proper citation: COBRApy (RRID:SCR_012096) Copy   


  • RRID:SCR_012095

    This resource has 1+ mentions.

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

A fast and accurate algorithm which allows to find a global alignment of multiple protein-protein interaction networks.

Proper citation: NetCoffee (RRID:SCR_012095) Copy   


https://cpndb.ca/

A curated collection of chaperonin sequence data collected from public databases or generated by a network of collaborators exploiting the cpn60 target in clinical, phylogenetic and microbial ecology studies. The database contains all available sequences for both group I and group II chaperonins. Users can search the database by Chaperonin type, group (I or II), BLAST, or other options, and can also enter and analyze FASTA sequences.

Proper citation: cpnDB: A Chaperonin Database (RRID:SCR_002263) Copy   


http://www.predictprotein.org/

Web application for sequence analysis and the prediction of protein structure and function. The user interface intakes protein sequences or alignments and returned multiple sequence alignments, motifs, and nuclear localization signals., THIS RESOURCE IS NO LONGER IN SERVICE. Documented on January 15,2026.

Proper citation: Predictions for Entire Proteomes (RRID:SCR_002803) Copy   


  • RRID:SCR_003499

    This resource has 100+ mentions.

http://regulondb.ccg.unam.mx/

Database on transcriptional regulation in Escherichia coli K-12 containing knowledge manually curated from original scientific publications, complemented with high throughput datasets and comprehensive computational predictions. Graphic and text-integrated environment with friendly navigation where regulatory information is always at hand. They provide integrated views to understand as well as organized knowledge in computable form. Users may submit data to make it publicly available.

Proper citation: RegulonDB (RRID:SCR_003499) Copy   


  • RRID:SCR_001892

    This resource has 1+ mentions.

http://statalign.github.io/

Software package for Bayesian analysis of protein, DNA and RNA sequences. It utilizes multiple alignments, phylogenetic trees and evolutionary parameters to quantify uncertainty in these analyses. It is written in Java.

Proper citation: StatAlign (RRID:SCR_001892) Copy   



Can't find your Tool?

We recommend that you click next to the search bar to check some helpful tips on searches and refine your search firstly. Alternatively, please register your tool with the SciCrunch Registry by adding a little information to a web form, logging in will enable users to create a provisional RRID, but it not required to submit.

Can't find the RRID you're searching for? X
  1. Neuroscience Information Framework Resources

    Welcome to the NIF Resources search. From here you can search through a compilation of resources used by NIF and see how data is organized within our community.

  2. Navigation

    You are currently on the Community Resources tab looking through categories and sources that NIF has compiled. You can navigate through those categories from here or change to a different tab to execute your search through. Each tab gives a different perspective on data.

  3. Logging in and Registering

    If you have an account on NIF then you can log in from here to get additional features in NIF such as Collections, Saved Searches, and managing Resources.

  4. Searching

    Here is the search term that is being executed, you can type in anything you want to search for. Some tips to help searching:

    1. Use quotes around phrases you want to match exactly
    2. You can manually AND and OR terms to change how we search between words
    3. You can add "-" to terms to make sure no results return with that term in them (ex. Cerebellum -CA1)
    4. You can add "+" to terms to require they be in the data
    5. Using autocomplete specifies which branch of our semantics you with to search and can help refine your search
  5. Save Your Search

    You can save any searches you perform for quick access to later from here.

  6. Query Expansion

    We recognized your search term and included synonyms and inferred terms along side your term to help get the data you are looking for.

  7. Collections

    If you are logged into NIF you can add data records to your collections to create custom spreadsheets across multiple sources of data.

  8. Sources

    Here are the sources that were queried against in your search that you can investigate further.

  9. Categories

    Here are the categories present within NIF that you can filter your data on

  10. Subcategories

    Here are the subcategories present within this category that you can filter your data on

  11. Further Questions

    If you have any further questions please check out our FAQs Page to ask questions and see our tutorials. Click this button to view this tutorial again.

X