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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
FunctSNP
 
Resource Report
Resource Website
FunctSNP (RRID:SCR_000393) FunctSNP software resource An R package for linking SNPs (Single Nucleotide Polymorphisms) to functional knowledge. single nucleotide polymorphism is listed by: OMICtools
has parent organization: SourceForge
PMID:20534127 Free, Available for download, Freely available OMICS_01925 SCR_000393 FunctSNP - Linking SNPs to functional knowledge 2026-09-12 12:55:08 0
LIPAGE
 
Resource Report
Resource Website
1+ mentions
LIPAGE (RRID:SCR_000290) data management software, software application, software resource Laboratory information management system for proteomics. The software works with 2DPAGE-based proteomics workflow. proteomics, laboratory, open source, 2dpage, management system is listed by: OMICtools
has parent organization: SourceForge
PMID:17018156 Free, Available for download, Freely available OMICS_02553 SCR_000290 LIMS for proteomics 2026-09-12 12:55:06 1
fourSig
 
Resource Report
Resource Website
fourSig (RRID:SCR_000516) software resource A suite of software programs for analyzing and visualizing 4C-seq data. standalone software, perl, r is listed by: OMICtools
has parent organization: SourceForge
PMID:24561615 Free, Available for download, Freely available OMICS_02628 SCR_000516 2026-09-12 12:55:11 0
TOPPAS
 
Resource Report
Resource Website
1+ mentions
TOPPAS (RRID:SCR_000533) software resource A graphical user interface (GUI) for rapid composition of HPLC-MS analysis workflows. Workflow construction is reduced to drag-and-drop of analysis tools and adding connections in between. gui, graphical user interface, analysis, hplc-ms, workflow is listed by: OMICtools
has parent organization: SourceForge
PMID:22583024 THIS RESOURCE IS NO LONGER IN SERVICE OMICS_02640 http://open-ms.sourceforge.net/workflow-integration/toppasworkflows/ SCR_000533 The OpenMS Proteomics Pipeline Assistant, TOPP Pipeline Assistant 2026-09-12 12:55:11 1
Ishtar
 
Resource Report
Resource Website
Ishtar (RRID:SCR_000538) software resource A program for designing primer pairs that amplify multiple target sequences using DNA thermodynamics and one class support vector machines. Written in Python. dna, thermodynamics, sequence, primer, pairs, loci, bioinformatics has parent organization: SourceForge Free, Available for download, Freely available, nlx_71525 SCR_000538 2026-09-12 12:55:11 0
Reprever
 
Resource Report
Resource Website
Reprever (RRID:SCR_000463) Reprever software resource Software that identifies (a) the insertion breakpoints where the extra duplicons inserted into the donor genome and (b) the actual sequence of the duplicon for any genomic regions that are increased in copy number. genomics, genomic region, insertion breakpoint, insertion, breakpoint, duplicon, genome is listed by: OMICtools
has parent organization: SourceForge
has parent organization: University of California at San Diego; California; USA
PMID:23658221 Free, Available for download, Freely available OMICS_01561 SCR_000463 Reprever: resolving low-copy duplicated sequences using template drive 2026-09-12 12:55:10 0
ViReMa
 
Resource Report
Resource Website
1+ mentions
ViReMa (RRID:SCR_000566) ViReMa data analysis software, data processing software, software application, software resource, software toolkit Software Python package for detection, alignment and reporting of recombination events in Next-Generation Sequencing data. Detects and reports recombination or fusion events in virus genomes using deep sequencing datasets. virus genomes deep sequencing datasets, detection, alignment and reporting of recombination events, Next-Generation Sequencing data, is listed by: OMICtools
has parent organization: SourceForge
has parent organization: Scripps Research Institute
PMID:24137010 Free, Available for download, Freely available, OMICS_00225 SCR_000566 Viral Recombination Mapper 2026-09-12 12:55:11 2
VariantMaster
 
Resource Report
Resource Website
VariantMaster (RRID:SCR_000569) VariantMaster software resource Software program that extracts causative variants in familial and sporadic genetic diseases. The algorithm takes into account predicted variants (SNPs and indels) in affected individuals or tumor samples and utilizes the row (BAM) data to robustly estimate the conditional probability of segregation in a family, as well as the probability of it being de novo or somatic. In familial cases, various modes of inheritance are considered: X-linked, autosomal dominant, and recessive (homozygosity or compound heterozygosity). Moreover, it integrates phenotypes and genotypes, and employs Annovar to produce additional information as allelic frequencies in general population and damaging scores. unix/linux, clinical, genetics, high throughput sequencing, monogenic disease, variant, snp, indel is listed by: OMICtools
has parent organization: SourceForge
Genetic disease, Tumor PMID:24389049 Free, Available for download, Freely available, OMICS_02261 SCR_000569 VariantMaster - Extract causative variants for monogenic and sporadic genetic diseases 2026-09-12 12:55:11 0
DeNovoGear
 
Resource Report
Resource Website
1+ mentions
DeNovoGear (RRID:SCR_000670) software resource A software for detecting de novo mutations using sequencing data. It utilizes likelihood-based error modeling to reduce the false positive rate of mutative discovery in exome analysis. It also uses fragment information to identify the parental origin of germ-line mutations. de novo, mutation, sequence, dna, rna, error modeling, exome analysis is listed by: OMICtools
has parent organization: SourceForge
has parent organization: Washington University School of Medicine in St. Louis; Missouri; USA
PMID:23975140 Free, Available for download, Freely available OMICS_00083 https://github.com/denovogear/denovogear SCR_000670 2026-09-12 12:55:13 3
SRMA
 
Resource Report
Resource Website
SRMA (RRID:SCR_000669) SRMA software resource A post-alignment micro re-aligner for next-generation high throughput sequencing data. matlab, sequence re-alignment, command-line, java, next generation sequencing, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: SourceForge
PMID:20932289 Free, Available for download, Freely available biotools:srma, OMICS_01079 https://bio.tools/srma SCR_000669 Short Read Micro re-Aligner 2026-09-12 12:55:13 0
FineSplice
 
Resource Report
Resource Website
1+ mentions
FineSplice (RRID:SCR_000691) software resource A software pipeline based on TopHat2 combined with a splice junction detection algorithm. standalone software, python is listed by: OMICtools
has parent organization: SourceForge
PMID:24574529 Free, Available for download, Freely available OMICS_03274 SCR_000691 2026-09-12 12:55:13 1
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 2026-09-12 12:57:56 23
Trowel
 
Resource Report
Resource Website
1+ mentions
Trowel (RRID:SCR_012890) Trowel software resource An error correction module for Illumina sequencing reads, which is based on the k-mer spectrum approach. c++, illumina, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: SourceForge
Apache License OMICS_01111, biotools:trowel https://bio.tools/trowel/ SCR_012890 Trowel - Error Correction Module for Illumina Sequencing Reads, Trowel - Sequencing Error Corrector 2026-09-12 12:57:54 5
Onco-STS
 
Resource Report
Resource Website
Onco-STS (RRID:SCR_012990) Onco-STS software resource Software for a web-based Laboratory Information Management System for sample and analysis tracking in oncogenomic experiments. is listed by: OMICtools
has parent organization: SourceForge
GNU General Public License, v3 OMICS_01008 SCR_012990 Onco-STS - A web-based Laboratory Information Management System 2026-09-12 12:57:56 0
NxGview
 
Resource Report
Resource Website
NxGview (RRID:SCR_012994) NxGview software resource A virtual software pipeline that contains several PERL modules for processing next generation sequencing data. is listed by: OMICtools
has parent organization: SourceForge
OMICS_01065 SCR_012994 2026-09-12 12:57:57 0
Bamformatics
 
Resource Report
Resource Website
1+ mentions
Bamformatics (RRID:SCR_013041) Bamformatics software resource Software that provides a coherent and consistent approach to analysis of high-throughput sequencing data. matlab is listed by: OMICtools
has parent organization: SourceForge
OMICS_00283 SCR_013041 Bamformatics - Toolkit and GUI for sequencing data analysis 2026-09-12 12:57:58 1
BSmapper
 
Resource Report
Resource Website
BSmapper (RRID:SCR_012998) BSmapper software resource Sequence mapper for bisulfite sequencing reads for DNA methylation studies. is listed by: OMICtools
has parent organization: SourceForge
GNU General Public License, v3 OMICS_00580 SCR_012998 2026-09-12 12:57:57 0
MendelScan
 
Resource Report
Resource Website
1+ mentions
MendelScan (RRID:SCR_013053) MendelScan software resource A software tool for prioritizing candidate variants in family-based studies of inherited disease. matlab is listed by: OMICtools
has parent organization: SourceForge
GNU General Public License, v2 OMICS_00065 SCR_013053 MendelScan - Variant scoring and linkage mapping for family exome sequencing 2026-09-12 12:57:58 4
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 2026-09-12 12:57:56 5
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 2026-09-12 12:57:56 0

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