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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.

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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
pyQPCR
 
Resource Report
Resource Website
pyQPCR (RRID:SCR_000471) pyQPCR software resource A GUI application written in python that deals with quantitative PCR (QPCR) raw data. Using quantification cycle values extracted from QPCR instruments, it uses a proven and universally applicable model to give finalized quantification resu quantitative pcr, python, qt is listed by: OMICtools
has parent organization: SourceForge
Free, Available for download, Freely available OMICS_02326 SCR_000471 2026-09-12 12:55:10 0
POPBAM
 
Resource Report
Resource Website
POPBAM (RRID:SCR_000464) POPBAM data analysis software, data processing software, software application, software resource A tool to perform evolutionary or population-based analyses of next-generation sequencing data. POPBAM takes a BAM file as its input and can compute many widely used evolutionary genetics measures in sliding windows across a genome. next-generation sequencing, evolution, population, bam, genome, evolutionary genetics, c++, short read, sequence alignment, sliding window, command-line, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: SourceForge
has parent organization: University of Rochester; New York; USA
PMID:24027417 Free, Available for download, Freely available biotools:popbam, OMICS_01559 https://bio.tools/popbam http://popbam.sourceforge.net/ SCR_000464 2026-09-12 12:55:10 0
drFAST
 
Resource Report
Resource Website
1+ mentions
drFAST (RRID:SCR_000586) drFAST software resource A software which maps di-base reads (SOLiD color space reads) to reference genome assemblies in a fast and memory-efficient manner. di-base, solid color space, genome assemblies, memory-efficient, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
is related to: SPLITREAD
has parent organization: SourceForge
PMID:21586516 Free, Available for download, Freely available biotools:drfast, OMICS_00661 https://bio.tools/drfast SCR_000586 di-base read Fast Alignment Search Tool, drFAST: di-base read Fast Alignment Search Tool 2026-09-12 12:55:11 1
GMcloser
 
Resource Report
Resource Website
1+ mentions
GMcloser (RRID:SCR_000646) GMcloser software resource Software that fills and closes the gaps present in scaffold assemblies, especially those generated by the de novo assembly of whole genomes with next-generation sequencing (NGS) reads. Unlike other gap-closing tools that use only NGS reads, GMcloser uses preassembled contig sets or long read sets as the sequences to close gaps and uses paired-end (PE) reads and a likelihood-based algorithm to improve the accuracy and efficiency of gap closure. The efficiency of gap closure can be increased by successive treatments with different contig sets. scaffolding, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: SourceForge
PMID:26261222 Free, Available for download, Freely available biotools:gmcloser, OMICS_00042 https://bio.tools/gmcloser SCR_000646 Gmcloser - Closing the gaps in scaffolds with preassembled contigs 2026-09-12 12:55:12 3
detecttd
 
Resource Report
Resource Website
detecttd (RRID:SCR_000681) detecttd software resource Software tool to detect tandem duplications in sequencing reads. It is written in Python and requires NCBI Blast standalone. tandem duplication, sequencing read, python, next-generation sequencing is listed by: OMICtools
has parent organization: SourceForge
THIS RESOURCE IS NO LONGER IN SERVICE OMICS_00315 SCR_000681 detecttd - Tool to detect tandem duplications in NGS reads 2026-09-12 12:55:13 0
FastUniq
 
Resource Report
Resource Website
1+ mentions
FastUniq (RRID:SCR_000682) software resource A software tool for removal of de novo duplicates in paired short DNA sequences. de novo, dna, sequence, duplicate, is listed by: OMICtools
has parent organization: SourceForge
DOI:10.1371/journal.pone.0052249 Free, Available for download, Freely available OMICS_01044 SCR_000682 2026-09-12 12:55:13 4
TriageTools
 
Resource Report
Resource Website
TriageTools (RRID:SCR_000675) TriageTools software resource A collection of tools for partitioning raw data (fastq reads) from high-throughput sequencing projects. The tools are designed for basic data management as well for prioritizing analysis of certain subsets. matlab, java, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: SourceForge
PMID:23408855 Free, Available for download, Freely available biotools:triagetools, nlx_156740 https://bio.tools/triagetools SCR_000675 2026-09-12 12:55:13 0
NGS tools for the novice
 
Resource Report
Resource Website
1+ mentions
NGS tools for the novice (RRID:SCR_000664) NGS tools for the novice software resource A collection of simple Perl scripts adressed to scientists doing research that bases on high throughput genomic/transcriptomic data. It does not require any bioinformatic expertise. The scripts perform fundamental processing steps like sorting sequences by TAGs, FASTQ to FASTA conversion, filtering and counting of redundant sequences, individually adjustable FASTQ quality filtering or basic analyses like base count and analysis of sequence length distribution. next generation sequencing, perl is listed by: OMICtools
has parent organization: SourceForge
Free, Available for download, Freely available OMICS_01063 SCR_000664 NGS tools for the novice - Handy tools for processing of next generation sequencing (NGS) data 2026-09-12 12:55:13 3
Opera
 
Resource Report
Resource Website
1+ mentions
Opera (RRID:SCR_000665) software resource A sequence assembly software program that uses information from paired-end reads to optimally order and orient contigs assembled from shotgun-sequencing reads. sequence assembly, paired-end, orient contigs, shotgun-sequencing, shotgun, software program, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: SourceForge
PMID:27169502
PMID:21929371
Free, Available for download, Freely available biotools:opera, OMICS_00045 https://bio.tools/opera SCR_000665 OPERA-LG, Optimal Paired-End Read Assembler 2026-09-12 12:55:13 3
AutoAssemblyD
 
Resource Report
Resource Website
AutoAssemblyD (RRID:SCR_001087) data analysis software, data processing software, sequence analysis software, software application, software resource Software which performs local and remote genome assembly by several assemblers based on an XML Template which can replace the large command lines required by most assemblers. genome, genome assembly, xml, sequence analysis software, local genome assembly, remote genome assembly, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: SourceForge
PMID:24143057 Free, Available for download, Freely available biotools:autoassemblyd, OMICS_00874 https://bio.tools/autoassemblyd SCR_001087 2026-09-12 12:55:19 0
ANDES
 
Resource Report
Resource Website
10+ mentions
ANDES (RRID:SCR_002791) data analysis software, data processing software, software application, software resource, software toolkit Software library and a suite of applications, written in Perl and R, for deep sequencing statistical analyses. deep sequencing, biomarker detection, statistical analysis, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: SourceForge
PMID:20633290 Free, Freely available, Available for download biotools:andes, OMICS_01119 https://bio.tools/andes SCR_002791 Statistical tools for the Analyses of Deep Sequencing (ANDES), Statistical tools for the Analyses of Deep Sequencing, Statistical tools for the ANalyses of Deep Sequencing 2026-09-12 12:55:46 26
GLProbs
 
Resource Report
Resource Website
1+ mentions
GLProbs (RRID:SCR_002739) software resource Software implementing a simple and effective approach to improve the accuracy of multiple sequence alignment. standalone software is listed by: OMICtools
has parent organization: SourceForge
PMID:26357079 Free, Freely available, Available for download OMICS_03732 SCR_002739 2026-09-12 12:55:45 1
Rainbow
 
Resource Report
Resource Website
10+ mentions
Rainbow (RRID:SCR_002724) data analysis software, data processing software, sequence analysis software, software application, software resource Software developed to provide an ultra-fast and memory-efficient solution to clustering and assembling short reads produced by RAD-seq. software, tool, clustering, assembling, short, read, restriction, site, DNA, sequence, analysis, bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
has parent organization: SourceForge
PMID:22942077
DOI:10.1093/bioinformatics/bts482
Free, Freely available, Available for download SCR_015992, OMICS_03722, biotools:rainbow https://bio.tools/rainbow, https://sources.debian.org/src/bio-rainbow/ SCR_002724 RAD-seq: Restriction-site Associated DNA sequencing, Bio-rainbow, RAD-seq 2026-09-12 12:55:45 41
rDock
 
Resource Report
Resource Website
100+ mentions
rDock (RRID:SCR_002838) software resource A fast and versatile Open Source docking software program that can be used to dock small molecules against proteins and nucleic acids. standalone software is listed by: OMICtools
has parent organization: SourceForge
PMID:24722481 Free, Freely available, Available for download OMICS_03835 SCR_002838 2026-09-12 12:55:47 122
FAS-DPD
 
Resource Report
Resource Website
FAS-DPD (RRID:SCR_003068) FAS-DPD software resource Software program to design degenerate primers for PCR. command-line, java, primer, pcr, degenerate primer is listed by: OMICtools
has parent organization: SourceForge
PMID:23533783 Free, Available for download, Freely available OMICS_02340 SCR_003068 family-specific degenerate primer design 2026-09-12 12:55:51 0
SALT
 
Resource Report
Resource Website
1000+ mentions
SALT (RRID:SCR_003187) SALT software resource Software that can accurately and sensitivity classify short reads of next-generation sequencing (NGS) into protein domain families. It is based on profile HMM and a supervised graph contribution algorithm. Compared to existing tools, it has high sensitivity and specificity in classifying short reads into their native domain families. next-generation sequencing, protein, protein domain, short read, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: SourceForge
PMID:23782615 Free, Available for download, Freely available OMICS_01565, biotools:salt https://bio.tools/salt SCR_003187 SALT - Protein domain classifier 2026-09-12 12:55:53 1307
XORRO
 
Resource Report
Resource Website
1+ mentions
XORRO (RRID:SCR_003181) XORRO software resource Efficient paired-read overlap software program for use with Illumina sequencing. illumina, next-generation sequencing is listed by: OMICtools
has parent organization: SourceForge
Free, Available for download, Freely available OMICS_01569 SCR_003181 XORRO: Rapid Paired-End Read Overlapper 2026-09-12 12:55:53 1
NovelSeq
 
Resource Report
Resource Website
NovelSeq (RRID:SCR_003136) NovelSeq software resource Software pipeline to detect novel sequence insertions using high throughput paired-end whole genome sequencing data. sequence, insertion, genome sequencing, genome, next-generation sequencing, illumina, unix, linux, c, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
is related to: SPLITREAD
has parent organization: Simon Fraser University; British Columbia; Canada
has parent organization: SourceForge
PMID:20385726 Free, Available for download, Freely available biotools:novelseq, nlx_156791, OMICS_02164 https://mybiosoftware.com/novelseq-1-0-2-sequence-insertions-detection.html#google_vignette SCR_003136 NovelSeq: Novel Sequence Insertion Detection 2026-09-12 12:55:52 0
mrCaNaVaR
 
Resource Report
Resource Website
10+ mentions
mrCaNaVaR (RRID:SCR_003135) mrCaNaVaR software resource Copy number caller that analyzes the whole-genome next-generation sequence mapping read depth to discover large segmental duplications and deletions. It also has the capability of predicting absolute copy numbers of genomic intervals. genome, next-generation sequence, duplication, deletion, copy number variant, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
is related to: SPLITREAD
has parent organization: SourceForge
Free, Freely available OMICS_02138, nlx_156790, biotools:mrcanavar https://bio.tools/mrcanavar SCR_003135 mrCaNaVaR - micro-read Copy Number Variant Regions, micro-read Copy Number Variant Regions 2026-09-12 12:55:52 16
JCVI Primer Designer
 
Resource Report
Resource Website
1+ mentions
JCVI Primer Designer (RRID:SCR_003275) JCVI Primer Designer software resource High throughput PCR primer design software. Target regions defined through a rich set of descriptors, such as Ensembl accessions and arbitrary genomic coordinates, may be specified. Primer pairs are then selected computationally to produce a minimal amplicon set capable of tiling across the specified target regions. As part of the tiling process, primer pairs are computationally screened to meet the criteria for success with one of two PCR amplification protocols. perl, command-line, pcr primer design, pcr, primer, high throughput sequencing is listed by: OMICtools
has parent organization: SourceForge
PMID:18405373 Free, Available for download, Freely available OMICS_02330 SCR_003275 2026-09-12 12:55:55 1

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