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.

Preparing word cloud

×

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

Filter by records added date
See new records

Options


Current Facets and Filters

  • Related Resources:sourceforge (facet)

Facets


Recent searches

Snippet view Table view
Click the to add this resource to a Collection

436 Results - per page

Show More Columns | Download 436 Result(s)

Resource Name Proper Citation Abbreviations Resource Type Description Keywords Resource Relationships Related Condition Funding Defining Citation Availability Website Status Alternate IDs Alternate URLs Old URLs Parent Organization Resource ID Synonyms Record Last Update Mentions Count
ProbeSelect
 
Resource Report
Resource Website
1+ mentions
ProbeSelect (RRID:SCR_012965) ProbeSelect software resource Software for selecting probes in heterogenous transcriptional sets. is listed by: OMICtools
has parent organization: SourceForge
OMICS_00836 SCR_012965 ProbeSelect - Selecting probes in heterogenous transcriptional sets 2026-02-14 02:02:48 4
SeqGenome Browser
 
Resource Report
Resource Website
SeqGenome Browser (RRID:SCR_012970) SeqGenome Browser software resource Mini cross-platform local genome browser software designed for visualizing next-generation sequencing data. c++ is listed by: OMICtools
has parent organization: SourceForge
GNU General Public License, v2 OMICS_00924 SCR_012970 2026-02-14 02:02:25 0
miRDeep-P
 
Resource Report
Resource Website
1+ mentions
miRDeep-P (RRID:SCR_013026) miRDP software resource A computational tool for analyzing the microRNA (miRNA) transcriptome in plants. is listed by: OMICtools
has parent organization: SourceForge
PMID:21775303 GNU General Public License, v3 OMICS_00375 SCR_013026 2026-02-14 02:02:45 6
KungFq
 
Resource Report
Resource Website
KungFq (RRID:SCR_012979) KungFq software resource Tool that compresses and decompresses fastq files. is listed by: OMICtools
has parent organization: SourceForge
PMID:23221092 OMICS_00962 SCR_012979 2026-02-14 02:02:25 0
ncPRO-seq
 
Resource Report
Resource Website
1+ mentions
ncPRO-seq (RRID:SCR_013031) ncPRO-seq software resource Software that aims to interrogate and perform detailed analysis on small RNAs derived from annotated non-coding regions. is listed by: OMICtools
has parent organization: SourceForge
PMID:23044543 OMICS_00366 SCR_013031 ncPRO-seq - A tool for annotation and profiling of ncRNAs from small RNA sequencing data 2026-02-14 02:02:45 9
vcf2MSAT
 
Resource Report
Resource Website
vcf2MSAT (RRID:SCR_013034) vcf2MSAT software resource A python software program to identify microsatellite repeat regions based on known polymorphisms identified in a .vcf report after using SAMtools to analyze next-generation sequencing files. is listed by: OMICtools
has parent organization: SourceForge
OMICS_00118 SCR_013034 vcf2MSAT - Find Microsatellites in a .vcf report 2026-02-14 02:02:26 0
FishingCNV
 
Resource Report
Resource Website
10+ mentions
FishingCNV (RRID:SCR_013038) FishingCNV software resource A software tool developed at McGill University, is a tool for comprehensive analysis of rare copy number variations in high-throughput exome sequencing data. is listed by: OMICtools
has parent organization: SourceForge
PMID:23539306 Commercial license OMICS_00334 SCR_013038 FishingCNV - Copy number variation detection in exome sequencing data, FishingCNV - CNV detection in exome sequencing data, FishingCNV - Copy number variation (CNV) detection in exome sequencing data 2026-02-14 02:02:26 11
MSAProbs
 
Resource Report
Resource Website
10+ mentions
MSAProbs (RRID:SCR_012982) MSAProbs software resource An open-source protein multiple sequence ailgnment algorithm, achieving the stastistically highest alignment accuracy on popular benchmarks. c++ is listed by: OMICtools
has parent organization: SourceForge
PMID:20576627 GNU General Public License, v3 OMICS_00980 SCR_012982 MSAProbs: Multiple Sequence Alignment 2026-02-14 02:02:45 19
QcReads
 
Resource Report
Resource Website
1+ mentions
QcReads (RRID:SCR_013002) QcReads software resource Provides an efficient tool for trimming adapter sequences and low quality sequences, in raw reads generated by the high throughput sequencing platforms. is listed by: OMICtools
has parent organization: SourceForge
OMICS_01088 SCR_013002 2026-02-14 02:02:20 1
HECTOR
 
Resource Report
Resource Website
50+ mentions
HECTOR (RRID:SCR_013007) HECTOR software resource A parallel multistage k-hopo spectrum based homopolymer-length error corrector for 454 sequencing data. is listed by: OMICtools
has parent organization: SourceForge
OMICS_01104 SCR_013007 HECTOR: Parallel error corrector for 454 datasets 2026-02-14 02:02:26 55
miRDeep*
 
Resource Report
Resource Website
10+ mentions
miRDeep* (RRID:SCR_012960) miRDeep* software resource An integrated application software tool for miRNA identification from RNA sequencing data. is listed by: OMICtools
has parent organization: SourceForge
PMID:23221645 GNU General Public License, v3, Acknowledgement requested OMICS_00374 SCR_012960 2026-02-14 02:02:25 23
AMOS
 
Resource Report
Resource Website
1000+ mentions
AMOS (RRID:SCR_013067) AMOS software resource A collection of tools and class interfaces for the assembly of DNA reads. bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
has parent organization: SourceForge
DOI:10.1093/bib/bbr074 OMICS_00008, biotools:amos https://bio.tools/amos
https://sources.debian.org/src/ampliconnoise/
SCR_013067 2026-02-14 02:02:27 4769
Contrail
 
Resource Report
Resource Website
1+ mentions
Contrail (RRID:SCR_013066) Contrail software resource A Hadoop based genome assembler for assembling large genomes in the clouds. mapreduce/hadoop is listed by: OMICtools
has parent organization: SourceForge
OMICS_00012 SCR_013066 2026-02-14 02:02:46 5
Easyfig
 
Resource Report
Resource Website
1000+ mentions
Easyfig (RRID:SCR_013169) Easyfig software resource A Python application for creating linear comparison figures of multiple genomic loci with an easy-to-use graphical user interface (GUI). is listed by: OMICtools
has parent organization: SourceForge
OMICS_00907 SCR_013169 2026-02-14 02:02:27 1101
ChimeraSlayer
 
Resource Report
Resource Website
100+ mentions
ChimeraSlayer (RRID:SCR_013283) ChimeraSlayer software resource A chimeric sequence detection utility, compatible with near-full length Sanger sequences and shorter 454-FLX sequences (~500 bp). bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: SourceForge
OMICS_01113, biotools:chimeraslayer https://bio.tools/chimeraslayer SCR_013283 2026-02-14 02:02:47 319
Telescoper
 
Resource Report
Resource Website
Telescoper (RRID:SCR_013206) Telescoper software resource An algorithm that iteratively extends long paths through a series of read-overlap graphs and evaluates them based on a statistical framework. bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
has parent organization: SourceForge
PMID:22962446 biotools:telescoper, OMICS_00036 https://bio.tools/telescoper SCR_013206 Telescoper - De novo assembly algorithm 2026-02-14 02:02:28 0
palfinder
 
Resource Report
Resource Website
1+ mentions
palfinder (RRID:SCR_013174) palfinder software resource A perl script that finds microsatellite repeat elements directly from raw 454 or Illumina paired-end sequencing reads. pacific biosciences is listed by: OMICtools
has parent organization: SourceForge
OMICS_00111 SCR_013174 2026-02-14 02:02:46 6
sam comp
 
Resource Report
Resource Website
sam comp (RRID:SCR_013179) sam_comp software resource A simple arithmetic coding based compressor for the SAM and BAM (DNA sequence alignment) file format. c++ is listed by: OMICtools
has parent organization: SourceForge
PMID:23533605 OMICS_00968 SCR_013179 2026-02-14 02:02:46 0
HeurAA
 
Resource Report
Resource Website
HeurAA (RRID:SCR_013212) HeurAA software resource Software for accurate and fast detection of genetic variations with a novel heuristic amplicon aligner program for next generation sequencing. unix/linux, bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
has parent organization: SourceForge
PMID:23349847 OMICS_00097, biotools:heuraa https://bio.tools/heuraa SCR_013212 heurAA - NGS multiplexed amplicon aligner 2026-02-14 02:02:28 0
bisReadMapper
 
Resource Report
Resource Website
bisReadMapper (RRID:SCR_013171) bisReadMapper software resource Fast and lightweight package for mapping bisulfite converted DNA sequencing reads from the Illumina platform. illumina is listed by: OMICtools
has parent organization: SourceForge
OMICS_00576 SCR_013171 bisReadMapper - Software for dealing with DNA methylation sequencing data 2026-02-14 02:02:50 0

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
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. Collections

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

  6. Facets

    Here are the facets that you can filter the data by.

  7. 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.