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| Resource Name | Proper Citation | Abbreviations | Resource Type |
Description |
Keywords | Resource Relationships | |||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
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DINDEL Resource Report Resource Website 10+ mentions |
DINDEL (RRID:SCR_001827) | Dindel | software application, software resource | THIS RESOURCE IS NO LONGER IN SERVICE. Documented on March 7,2024. Software program for calling small indels from short-read sequence data ("next generation sequence data"). It is currently designed to handle only Illumina data. Dindel takes BAM files with mapped Illumina read data and enables researchers to detect small indels and produce a VCF file of all the variant calls. It has been written in C++ and can be used on Linux-based and Mac computers (it has not been tested on Windows operating systems). | indel, short-read, next generation sequence, illumina, gene, genetic, genomic, c++, linux, macos, bio.tools |
is listed by: OMICtools is listed by: Genetic Analysis Software is listed by: bio.tools is listed by: Debian has parent organization: Wellcome Trust Sanger Institute; Hinxton; United Kingdom |
PMID:20980555 DOI:10.1101/gr.112326.110 |
THIS RESOURCE IS NO LONGER IN SERVICE | , nlx_154283, OMICS_00096, biotools:dindel | https://bio.tools/dindel, https://sources.debian.org/src/dindel/ | http://www.sanger.ac.uk/resources/software/dindel/ | SCR_001827 | Dindel: Accurate indel calls from short-read data | 2026-09-19 12:57:44 | 44 | ||||
|
PEDIGRAPH Resource Report Resource Website 10+ mentions |
PEDIGRAPH (RRID:SCR_001938) | Pedigraph | software application, software resource | A pedigree visualization program specifically designed to draw large, complex pedigrees. (entry from Genetic Analysis Software) Options include: * Full pedigree * Summarization * Extraction of individual pedigrees * Inbreeding calculation * Coancestry coefficient calculation * Color control * Drawing size * Page size and margins * Drawing styles | gene, genetic, genomic, c, c++, ms-windows, linux, pedigree, java, bio.tools |
is listed by: OMICtools is listed by: Genetic Analysis Software is listed by: bio.tools is listed by: Debian has parent organization: University of Minnesota Twin Cities; Minnesota; USA |
PMID:14986440 | Acknowledgement required, Copyrighted | biotools:pedigraph, OMICS_00212, nlx_154519 | https://bio.tools/pedigraph | SCR_001938 | 2026-09-19 12:57:44 | 17 | ||||||
|
NBRC Resource Report Resource Website 500+ mentions |
NBRC (RRID:SCR_002660) | NBRC | biomaterial supply resource, material resource | Collection of microbial resources and perform taxonomic characterization of individual microorganisms such as bacteria including actinomycetes and archaea, yeasts, fungi, algaes, bacteriophages and DNA resources for academic research and industrial applications. NBRC is a member of WFCC, OECD Global BRC Network, ACM and JSCC. They are certified by quality management system ISO 9001. To provide attractive biological resources with useful information attached, they actively collect potentially useful biological resources (microorganisms and cloned genes) and distributes them to promote basic research as well as industrial applications. At the Biological Resource Center, they explore, isolate and identify microorganisms from various natural environments and at the same time accept scientifically and industrially useful microorganisms from researchers in academic and industrial sectors. The microbial DNA library constructed at the Biotechnology Development Center is also part of their collection. To improve and expand the collection, new methodologies for the isolation, identification and preservation of microorganisms and DNA will be investigated and developed so as to provide biological resources of higher quality. Their resources serve, for example, as the standard for determining antimicrobial activity, in aseptic tests as well as for the production of pharmaceutical substances and will be constantly reinforced for wider distribution to researchers in academia and industries. Please refer to the catalog shown at the NBRC website for details. | cdna clone, dna, clone, human, oligo-capping, microbial, genomic, cdna, FASEB list | is listed by: One Mind Biospecimen Bank Listing | Restricted | nif-0000-22391 | SCR_002660 | National Institute of Technology and Evaluation Biological Resource Center, NITE Biological Resource Center, Biological Resource Center NITE | 2026-09-19 12:57:46 | 866 | |||||||
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Conrad Prebys Center for Chemical Genomics Resource Report Resource Website |
Conrad Prebys Center for Chemical Genomics (RRID:SCR_001687) | data or information resource, organization portal, portal | The Conrad Prebys Center for Chemical Genomics (CPCCG) uses advanced screening technologies to identify high level chemical probes that interact with proteins involved in cellular processes. Optimization of these probes using medicinal chemistry and informatics will form the basis of a new generation of medicines. CPCCG is 1 of 4 Comprehensive Centers chosen nationally to be a part of the Molecular Libraries Probe Program (MLP), which established the Molecular Libraries Probe Production Centers Network (MLPCN). The goal is to produce small molecule probes that allow research into health and disease on the cellular level. CPCCG core services span a range of biochemical and cell-based screens for obtaining hits and provide chemistry resources for optimizing hits into probes or drug development. - Full scale screening capabilities and technology which can provide rapid screening on a broad diversity of assays and detection platforms - Several fully-integrated industrial-scale high-throughput screening (HTS) workstations - HTS microscopy/HCS and novel algorithm development for image analysis - Full hit-to-probe chemistry and exploratory pharmacology - Powerful NMR based Chemical Fragment Screening - Highly integrated informatics infrastructure and efficient data mining capabilities - Protein production facility - Cell production facility for scale-up tissue culture The CPCCG Screening Core can screen 96, 384 or 1536 well formats using either biochemical or cell-based assays, and can process over 300,000 wells per day. Total throughput capacity will climb to over 2 million compounds per day following the opening of Burnhams east coast campus in Lake Nona, Florida. | drug, algorithm, analysis, assay, biochemical, cell, cellular, chemical, culture, development, disease, genomic, hcs, health, hts microscopy, keywords: chemical, medicinal, microscopy, molecular, molecule, probe, process, production, protein, technology, tissue, image | Free, Freely Available | nif-0000-10180 | http://sdccg.burnham.org | SCR_001687 | CPCCG | 2026-09-19 12:55:50 | 0 | ||||||||
|
SoftBerry Resource Report Resource Website 100+ mentions |
SoftBerry (RRID:SCR_000902) | data or information resource, portal, software resource | Developer of software tools for genomic research focused on computational methods of high throughput biomedical data analysis, including software to support next generation sequencing technologies, transcriptome analysis with RNASeq data, SNP detection and selection of disease specific SNP subsets. Provides custom genome annotation services. | genomic, analysis, computation, biomedical, data analysis, rnaseq, sna, snp, transcriptome | Restricted | nlx_156881 | http://linux1.softberry.com/ | SCR_000902 | Linux SoftBerry, Soft berry | 2026-09-19 12:55:49 | 356 | ||||||||
|
SOAP Resource Report Resource Website 100+ mentions |
SOAP (RRID:SCR_000689) | SOAP, | data processing software, software application, software resource | Software package that provides full solution to next generation sequencing data analysis consisting of an alignment tool (SOAPaligner/soap2), a re-sequencing consensus sequence builder (SOAPsnp), an indel finder ( SOAPindel ), a structural variation scanner ( SOAPsv ), a de novo short reads assembler ( SOAPdenovo ), and a GPU-accelerated alignment tool for aligning short reads with a reference sequence. (SOAP3/GPU)., THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025. | gene, genetic, genomic, next generation sequencing, alignment, short read, bio.tools |
lists: SOAPfusion lists: SOAPfuse lists: SOAPnuke lists: GapCloser is listed by: Genetic Analysis Software is listed by: bio.tools is listed by: Debian has parent organization: BGI; Shenzhen; China is parent organization of: SOAP3 is parent organization of: SOAPaligner/soap2 |
PMID:18227114 | THIS RESOURCE IS NO LONGER IN SERVICE | nlx_154652, biotools:soap | https://bio.tools/soap | SCR_000689 | SOAP: short oligonucleotide alignment program, Short Oligonucleotide Analysis Package | 2026-09-19 12:55:49 | 403 | |||||
|
PSEUDOMARKER Resource Report Resource Website 10+ mentions |
PSEUDOMARKER (RRID:SCR_009345) | PSEUDOMARKER | software application, software resource | A linkage analysis software for joint linkage and/or linkage disequilibrium analysis. PSEUDOMARKER can analyze different data structures jointly such as cases-controls, trios, sib-pairs, sib-ships, and extended families. (entry from Genetic Analysis Software) | gene, genetic, genomic, c/c++, linux | is listed by: Genetic Analysis Software | nlx_154557 | SCR_009345 | 2026-09-19 12:58:04 | 14 | |||||||||
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PRT Resource Report Resource Website |
PRT (RRID:SCR_009340) | PRT | software application, software resource | Software application for partition of single generation into sibling groups (entry from Genetic Analysis Software) | gene, genetic, genomic, ms-windows | is listed by: Genetic Analysis Software | nlx_154554 | SCR_009340 | Pedigree Reconstruction Tools | 2026-09-19 12:58:04 | 0 | ||||||||
|
PSAT Resource Report Resource Website 10+ mentions |
PSAT (RRID:SCR_009341) | PSAT | software application, software resource | Software application (entry from Genetic Analysis Software) | gene, genetic, genomic | is listed by: Genetic Analysis Software | nlx_154555 | SCR_009341 | Population Stratification Association Test | 2026-09-19 12:58:04 | 29 | ||||||||
|
SELSIM Resource Report Resource Website 1+ mentions |
SELSIM (RRID:SCR_009378) | software application, software resource | Software program which can simulate population genetic data in which a single site has experienced natural selection. When designing methods which provide the necessary power to detect regions of the genome which have experience historical selective pressures it is important to consider which patterns of genetic diversity are indicative of particular forms of natural selection. (entry from Genetic Analysis Software) | gene, genetic, genomic, c, c++, ms-windows, (xp), linux | is listed by: Genetic Analysis Software | nlx_154613 | http://www.stats.ox.ac.uk/mathgen/software.html | SCR_009378 | SelSim | 2026-09-19 12:58:05 | 2 | ||||||||
|
R/ONEMAP Resource Report Resource Website 10+ mentions |
R/ONEMAP (RRID:SCR_009371) | software application, software resource | Software environment for constructing linkage maps in outcrossing plant species, using full-sib families derived from two outbreed (non-inbreeding) parent plants. (entry from Genetic Analysis Software) | gene, genetic, genomic, r | is listed by: Genetic Analysis Software | nlx_154502, SCR_009312, nlx_154593 | http://www.ciagri.usp.br/~aafgarci/OneMap/ | SCR_009371 | ONEMAP | 2026-09-19 12:58:05 | 22 | ||||||||
|
SPAM Resource Report Resource Website 100+ mentions |
SPAM (RRID:SCR_009407) | software application, software resource | Software application that estimates the relative contributions of discrete populations to a mixture sample, solving what is commonly referred to in fisheries as the mixed stock analysis or genetic stock identification problem. (entry from Genetic Analysis Software) | gene, genetic, genomic | is listed by: Genetic Analysis Software | nlx_154654 | SCR_009407 | Statistics Program for Analysing Mixtures | 2026-09-19 12:58:06 | 154 | |||||||||
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SNPTEST Resource Report Resource Website 100+ mentions |
SNPTEST (RRID:SCR_009406) | software application, software resource | Software program for the analysis of single SNP association in genome-wide studies. The tests implemented can cater for binary (case-control) and quantitative phenotypes, can condition upon an arbitrary set of covariates and properly account for the uncertainty in genotypes. The program is designed to work seamlessly with the output of both the genotype calling program CHIAMO, the genotype imputation program IMPUTE and the program GTOOL. This program was used in the analysis of the 7 genome-wide association studies carried out by the Wellcome Trust Case-Control Consortium (WTCCC). (entry from Genetic Analysis Software) | gene, genetic, genomic, bio.tools |
is listed by: Genetic Analysis Software is listed by: bio.tools is listed by: Debian |
nlx_154651, biotools:snptest | https://bio.tools/snptest | http://www.stats.ox.ac.uk/~marchini/software/gwas/snptest.html | SCR_009406 | 2026-09-19 12:58:06 | 401 | ||||||||
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SNPLINK Resource Report Resource Website 1+ mentions |
SNPLINK (RRID:SCR_009403) | software application, software resource | Software application for multipoint linkage analysis of densely distributed SNP data incorporating automated linkage disequilibrium removal. SNPLINK requires these other programs installed on the system: MERLIN (used for nonparametric analysis), ALLEGRO (used for parametric analysis), R and PERL, all are freely available. (entry from Genetic Analysis Software) | gene, genetic, genomic, perl, unix | is listed by: Genetic Analysis Software | nlx_154646 | SCR_009403 | 2026-09-19 12:58:06 | 4 | ||||||||||
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SNPP Resource Report Resource Website 50+ mentions |
SNPP (RRID:SCR_009404) | software application, software resource | THIS RESOURCE IS NO LONGER IN SERVICE, documented September 29, 2016. A dynamic general database management system to manage high-throughput SNP genotyping data. It provides several functions, including data importing with comparison, Mendelian inheritance check within pedigrees, data compiling and exporting. Furthermore, SNPP may generate files for repeat genotyping and transform them into files that can be executed by a liquid handling system. | gene, genetic, genomic, java, windows, linux, solaris, macos | is listed by: Genetic Analysis Software | THIS RESOURCE IS NO LONGER IN SERVICE | nlx_154648 | SCR_009404 | Single Nucleotide Polymorphism Processor | 2026-09-19 12:58:06 | 60 | ||||||||
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R/LUCA Resource Report Resource Website |
R/LUCA (RRID:SCR_009369) | R/LUCA | software application, software resource | Software application (entry from Genetic Analysis Software) | gene, genetic, genomic | is listed by: Genetic Analysis Software | nlx_154591 | http://stat-db.stat.sfu.ca:8080/statgen/research/luca/ | SCR_009369 | Likelihood Under Covariate Assumptions | 2026-09-19 12:58:05 | 0 | |||||||
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SNAP 3 Resource Report Resource Website 1+ mentions |
SNAP 3 (RRID:SCR_009400) | software application, software resource | THIS RESOURCE IS NO LONGER IN SERVICE, documented September 29, 2016. Software program can be used to generate SNP haplotype sequence data of unrelated individuals and nuclear families with a fixed or random number of children. | gene, genetic, genomic, c, linux, unix, solaris, ms-windows | is listed by: Genetic Analysis Software | THIS RESOURCE IS NO LONGER IN SERVICE | nlx_154639 | http://capella.uni-kiel.de/snap/snap.htm, | SCR_009400 | Simulation of sNp haplotype data And Phenotypic traits | 2026-09-19 12:58:06 | 1 | |||||||
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R/GAP Resource Report Resource Website 1+ mentions |
R/GAP (RRID:SCR_009364) | R/GAP | software application, software resource | An integrated software package for genetic data analysis of both population and family data. Currently it contains functions for sample size calculations of both population-based and family-based designs, classic twin ACE/ADE/AE/CE models, probability of familial disease aggregation, kinship calculation, some statistics in linkage analysis, and association analysis involving one or more genetic markers including haplotype analysis with or without environmental covariates (entry from Genetic Analysis Software) | gene, genetic, genomic, r | is listed by: Genetic Analysis Software | nlx_154583 | SCR_009364 | R/Genetic Analysis Package | 2026-09-19 12:58:05 | 1 | ||||||||
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R/HAPASSOC Resource Report Resource Website |
R/HAPASSOC (RRID:SCR_009365) | software application, software resource | Software application using a likelihood approach to inference of haplotype and nongenetic effects and their interactions in generalized linear models of disease penetrance, when haplotype phase is unknown for some subjects. Parameter estimates are obtained by use of an expectation-maximization (EM) algorithm and standard errors are calculated using Louis'' formula. (entry from Genetic Analysis Software) | gene, genetic, genomic, r | is listed by: Genetic Analysis Software | nlx_154587, SCR_009219, nlx_154374 | http://stat-db.stat.sfu.ca:8080/statgen/research/hapassoc | SCR_009365 | HAPASSOC | 2026-09-19 12:58:05 | 0 | ||||||||
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RHMAP Resource Report Resource Website 1+ mentions |
RHMAP (RRID:SCR_009360) | RHMAP | software application, software resource | Software application (entry from Genetic Analysis Software) | gene, genetic, genomic, fortran77 | is listed by: Genetic Analysis Software | nlx_154575 | SCR_009360 | Radiation Hybrid Map | 2026-09-19 12:58:05 | 3 |
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