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

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

  • Keywords:bio.tools (facet)

Facets


Recent searches

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

1,647 Results - per page

Show More Columns | Download Top 1000 Results

Resource Name Proper Citation Abbreviations Resource Type Description Keywords Resource Relationships Related Condition Funding Defining Citation Availability Specification URL Alternate IDs Alternate URLs Old URLs Parent Organization Resource ID Synonyms Record Last Update Mentions Count
hyfi: software suite for binding site search
 
Resource Report
Resource Website
hyfi: software suite for binding site search (RRID:SCR_004884) software resource This collection of software is designed to rapidly identify identifies primer and microarray probe binding sites for a query sequence in genomic DNA. This software suite has four main programs:1. A program for indexing a sequence file to speed up the binding site search. 2. A program for retrieving the binding sites of a query sequence. 3. A program for identifying sites where PCR primers could co-operate to exponentially amplify a sequence 4. A program for analyzing a set of binding sites to tailor the search for different reaction conditions. This software is implemented in C. bio.tools is listed by: bio.tools
is listed by: Debian
has parent organization: University of Washington; Seattle; USA
PMID:16873493 nlx_85657, biotools:hyfi https://bio.tools/hyfi SCR_004884 Hyfi 2026-08-01 12:02:46 0
USeq
 
Resource Report
Resource Website
100+ mentions
USeq (RRID:SCR_004753) USeq software resource A collection of software tools for for both low and high level analysis of next generation, ultra high throughput signature sequencing data from the Solexa, SOLiD, and 454 platforms. bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: SourceForge
OMICS_00499, biotools:useq https://bio.tools/useq SCR_004753 2026-08-01 12:02:45 124
miRNAKey
 
Resource Report
Resource Website
1+ mentions
miRNAKey (RRID:SCR_004813) miRNAKey software resource A software pipeline for the analysis of microRNA Deep Sequencing data. bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
PMID:20801911 OMICS_00364, biotools:mirnakey https://bio.tools/mirnakey SCR_004813 2026-08-01 12:02:45 6
SVMerge
 
Resource Report
Resource Website
10+ mentions
SVMerge (RRID:SCR_004777) SVMerge software resource Software pipeline to detect structural variants (SVs) by integrating calls from several existing SV callers, which are then validated and the breakpoints refined using local de novo assembly. The output is in BED format allowing for easy downstream analysis or viewing in a genome browser. It is modular and extensible allowing new callers to be incorporated as they become available. structural variant, breakpoint, bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
has parent organization: SourceForge
has parent organization: Wellcome Trust Sanger Institute; Hinxton; United Kingdom
PMID:21194472 biotools:svmerge, OMICS_00325 https://bio.tools/svmerge SCR_004777 SVMerge - Enhanced structural variant and breakpoint detection 2026-08-01 12:02:40 19
SVseq
 
Resource Report
Resource Website
1+ mentions
SVseq (RRID:SCR_004804) SVseq software resource Software for accurate and efficient calling of structural variations with low-coverage sequence data. Version 2 uses the BAM files of paired Illumina reads with soft-clip signature as input. It calls both deletions and insertions. structural variant, deletion, insertion, breakpoint, bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
has parent organization: University of Connecticut; Connecticut; USA
PMID:22537045 OMICS_00327, biotools:svseq https://bio.tools/svseq SCR_004804 SVseq2, SVseq1 2026-08-01 12:02:46 3
mrsFAST
 
Resource Report
Resource Website
10+ mentions
mrsFAST (RRID:SCR_003128) mrsFAST software resource A cache-oblivious algorithm designed to map short reads to reference genome assemblies in a fast and memory-efficient manner. It optimizes cache usage to get higher performance. Currently Supported Features: * Mistmatches, No indels * Paired-end Mapping Mode * Discordant Paired-end Mapping Mode (to be used in conjuction with Variation Hunter) next-generation sequencing, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
is related to: SPLITREAD
has parent organization: SourceForge
PMID:20676076 Free, Available for download, Freely available biotools:mrsfast, nlx_156780 https://bio.tools/mrsfast SCR_003128 mrsFAST: micro-read substitution-only Fast Alignment Search Tool, micro-read substitution-only Fast Alignment Search Tool 2026-08-01 12:02:03 20
HYDEN
 
Resource Report
Resource Website
10+ mentions
HYDEN (RRID:SCR_003126) HYDEN software resource Software program for designing pairs of degenerate primers for a given set of DNA sequences. It works well for large input sets of genomic sequences (e.g., hundreds of sequences of length 1Kbp). It is a batch (i.e., command-line, as opposed to graphical interface) program, available for Windows XP (downloadable version) and Linux (upon request). degenerate, primer, dna sequence, primer design, degenerate primer, windows, linux, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: Tel Aviv University; Ramat Aviv; Israel
PMID:17951798 Free, Available for download, Freely available OMICS_02338, biotools:hyden https://bio.tools/hyden SCR_003126 HYDEN - A Software for Designing Degenerate Primers, HighlY DEgeNerate primers 2026-08-01 12:02:17 12
QDNAseq
 
Resource Report
Resource Website
100+ mentions
QDNAseq (RRID:SCR_003174) software resource Software package for quantitative DNA sequencing for chromosomal aberrations providing a robust, cost-effective WGS method for DNA copy number analysis. The genome is divided into non-overlapping fixed-sized bins, number of sequence reads in each counted, adjusted with a simultaneous two-dimensional loess correction for sequence mappability and GC content, and filtered to remove spurious regions in the genome. Downstream steps of segmentation and calling are also implemented via packages DNAcopy and CGHcall, respectively. software package, unix/linux, mac os x, windows, r, copy number variation, dna-seq, genetics, genome annotation, preprocessing, quality control, sequencing, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
PMID:25236618 Free, Available for download, Freely available OMICS_05902, biotools:qdnaseq https://github.com/ccagc/QDNAseq, https://bio.tools/qdnaseq SCR_003174 QDNAseq - Quantitative DNA sequencing for chromosomal aberrations 2026-08-01 12:02:17 150
miR-PREFeR
 
Resource Report
Resource Website
1+ mentions
miR-PREFeR (RRID:SCR_003353) software resource An accurate, fast, and easy-to-use plant miRNA prediction software tool using small RNA-Seq data. It utilizes expression patterns of miRNA and follows the criteria for plant microRNA annotation to accurately predict plant miRNAs from one or more small RNA-Seq data samples of the same species. standalone software, bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
PMID:24930140 Free, Available for download, Freely available biotools:mir-prefer, OMICS_04637 https://bio.tools/mir-prefer SCR_003353 miRNA PREdiction From small RNA-Seq data, miR-PREFeR: microRNA PREdiction From small RNAseq data 2026-08-01 12:02:29 7
PicTar
 
Resource Report
Resource Website
1000+ mentions
PicTar (RRID:SCR_003343) PicTar software resource An algorithm for the identification of microRNA targets. Details are provided (3' UTR alignments with predicted sites, links to various public databases etc) regarding: # microRNA target predictions in vertebrates (Krek et al, Nature Genetics 37:495-500 (2005)) # microRNA target predictions in seven Drosophila species (Grn et al, PLoS Comp. Biol. 1:e13 (2005)) # microRNA targets in three nematode species (Lall et al, Current Biology 16, 1-12 (2006)) # human microRNA targets that are not conserved but co-expressed (i.e. the microRNA and mRNA are expressed in the same tissue) (Chen and Rajewsky, Nat Genet 38, 1452-1456 (2006)) co-expressed targets microrna target, microrna, bio.tools, FASEB list is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
is listed by: SoftCite
is related to: UCSC Genome Browser
has parent organization: Max Delbruck Center for Molecular Medicine; Berlin; Germany
PMID:15806104 Free, Available for download, Freely available OMICS_00411, biotools:pictar, nif-0000-31983 http://pictar.mdc-berlin.de/, https://bio.tools/pictar SCR_003343 2026-08-01 12:02:20 1636
Assembly Based ReAligner
 
Resource Report
Resource Website
1+ mentions
Assembly Based ReAligner (RRID:SCR_003277) ABRA software resource Software that is a realigner for next generation sequencing data. It uses localized assembly and global realignment to align reads more accurately, thus improving downstream analysis (detection of indels and complex variants in particular). standalone software, c, c++, java, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
PMID:24907369 Free, Available for download, Freely available OMICS_04668, biotools:abra https://bio.tools/abra SCR_003277 ABRA - Assembly Based ReAligner 2026-08-01 12:02:29 7
NormqPCR
 
Resource Report
Resource Website
50+ mentions
NormqPCR (RRID:SCR_003388) NormqPCR software resource Software package providing functions for the selection of optimal reference genes and the normalization of real-time quantitative PCR data. gene expression, microtitre plate assay, qpcr, reference gene, bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
has parent organization: Bioconductor
PMID:22748112 Free, Available for download, Freely available OMICS_02315, biotools:normqpcr https://bio.tools/normqpcr SCR_003388 NormqPCR - Functions for normalisation of RT-qPCR data 2026-08-01 12:02:20 51
PoPoolation
 
Resource Report
Resource Website
100+ mentions
PoPoolation (RRID:SCR_003495) PoPoolation software resource A collection of tools to facilitate population genetic studies of next generation sequencing data from pooled individuals. It builds upon open source tools (bwa, samtools) and uses standard file formats (gtf, sam, pileup) to ensure a wide compatibility. PoPoolation allows to calculate Tajima's Pi, Watterson's Theta and Tajima's D for reference sequences using a sliding window approach. Alternatively these population genetic estimators may be calculated for a set of genes (provided as gtf). One of the main challenges in population genomics is to identify regions of intererest on a genome wide scale. PoPoolation will greatly aid this task by allowing a fast and user friendly analysis of NGS data from DNA pools. population genetics, next generation sequencing, sliding window, genome, bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
has parent organization: Google Code
PMID:21253599 Acknowledgement requested OMICS_04414, biotools:popoolation https://bio.tools/popoolation SCR_003495 2026-08-01 12:02:13 139
GEPAT
 
Resource Report
Resource Website
1+ mentions
GEPAT (RRID:SCR_003597) GEPAT software resource A web-based software tool offering an integrated analysis of transcriptome data under genomic, proteomic and metabolic context. bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: SourceForge
PMID:17543125 OMICS_00765, biotools:gepat https://bio.tools/gepat SCR_003597 Genome Expression Pathway Analysis Tool 2026-08-01 12:02:15 2
J-Express
 
Resource Report
Resource Website
50+ mentions
J-Express (RRID:SCR_003609) J-Express software resource Gene expression analysis software using Java. bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
is parent organization of: Mini Analysis Guide for Microarrays
PMID:11301307 Acknowledgement requested biotools:j-express, OMICS_00767 https://bio.tools/j-express SCR_003609 J-Express: Gene expression analysis software 2026-08-01 12:02:32 86
AmpliconNoise
 
Resource Report
Resource Website
50+ mentions
AmpliconNoise (RRID:SCR_007814) AmpliconNoise software resource A collection of programs for the removal of noise from 454 sequenced PCR amplicons. This project also includes the Perseus algorithm for chimera removal. bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
has parent organization: Google Code
DOI:10.1186/1471-2105-12-38 biotools:pyronoise, OMICS_01112 https://bio.tools/pyronoise, https://sources.debian.org/src/anfo/ SCR_007814 2026-08-01 12:03:34 90
Minia
 
Resource Report
Resource Website
50+ mentions
Minia (RRID:SCR_004986) Minia software resource A short-read assembler based on a de Bruijn graph, capable of assembling a human genome on a desktop computer in a day. bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
DOI:10.1186/1748-7188-8-22 biotools:minia, OMICS_00022 https://bio.tools/minia, https://sources.debian.org/src/minia/ SCR_004986 2026-08-01 12:02:43 62
MIP Scaffolder
 
Resource Report
Resource Website
1+ mentions
MIP Scaffolder (RRID:SCR_005072) MIP Scaffolder software resource A software program for scaffolding contigs produced by fragment assemblers using mate pair data such as those generated by ABI SOLiD or Illumina Genome Analyzer. scaffolding, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: University of Helsinki; Helsinki; Finland
OMICS_00044, biotools:mip_scaffolder https://bio.tools/mip_scaffolder SCR_005072 2026-08-01 12:02:53 1
T-lex
 
Resource Report
Resource Website
1+ mentions
T-lex (RRID:SCR_005134) T-lex software resource Software package for fast and accurate discovery, annotation, re-annotation and population analysis of Transposable Elements using Next-Generation Sequencing data. transposable element, next-generation sequencing, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: Stanford University; Stanford; California
has parent organization: SourceForge
GNU General Public License biotools:t-lex2, OMICS_00121 https://bio.tools/t-lex2 SCR_005134 T-lex package 2026-08-01 12:02:46 4
ERANGE
 
Resource Report
Resource Website
10+ mentions
ERANGE (RRID:SCR_005240) ERANGE software resource Software for Mapping and Quantifying Mammalian Transcriptomes by RNA-Seq. Its functions are to (i) assign reads that map uniquely in the genome to their site of origin and, for reads that match equally well to several sites (''multireads''), assign them to their most likely site(s) of origin; (ii) detect splice-crossing reads and assign them to their gene of origin; (iii) organize reads that cluster together, but do not map to an already known exon, into candidate exons or parts of exons; and (iv) calculate the prevalence of transcripts from each known or newly proposed RNA, based on normalized counts of unique reads, spliced reads and multireads. The new candidate RNA regions produced can be thought of as ESTs, and, like ESTs, some are provisionally appended to existing gene models if they meet several additional criteria. Remaining unassigned candidate transcribed regions (labeled RNAFAR features) can then be used in conjunction with other confirming data to develop new or revised gene models. transcriptome, rna-seq, bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
PMID:18516045 OMICS_01274, biotools:erange https://bio.tools/erange SCR_005240 Enhanced Read Analysis of Gene Expression 2026-08-01 12:02:58 30

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. RRID Portal Resources

    Welcome to the RRID Resources search. From here you can search through a compilation of resources used by RRID 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 RRID 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 RRID then you can log in from here to get additional features in RRID 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 RRID 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.