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| Resource Name | Proper Citation | Abbreviations | Resource Type |
Description |
Keywords | Resource Relationships | |||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
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ROSATTA SYLLEGO SYSTEM Resource Report Resource Website |
ROSATTA SYLLEGO SYSTEM (RRID:SCR_009363) | Syllego system | software resource, software application | THIS RESOURCE IS NO LONGER IN SERVICE, documented on August 2, 2014. A genetic data management and analysis system designed to advance your whole genome association, linkage, and eQTL studies, providing you with an easy-to-use project workspace so that you can organize, analyze, and share your genotype and phenotype data along with your analysis results. With the Syllego system, generating high quality analysis data and meaningful results becomes simple. The Syllego system automates all tedious data management and data formatting tasks so that you can streamline your genetic analysis workflows using your analysis methods of choice. Managing all your genetic data and reference information is straightforward. The Syllego system converts public and private genotype data sets and reference annotations, such as dbSNP and HapMap, as well as individual (sample) information into a single, consistent repository for fast, convenient access. (entry from Genetic Analysis Software) | gene, genetic, genomic | is listed by: Genetic Analysis Software | THIS RESOURCE IS NO LONGER IN SERVICE | nlx_154578 | SCR_009363 | 2026-02-14 02:07:06 | 0 | ||||||||
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ROMPREV Resource Report Resource Website |
ROMPREV (RRID:SCR_009361) | ROMPREV | software resource, software application | Software tool for testing for association between polymorphisms and quantitative traits, as well as estimating trait heritability and locus-specific heritability using family data. (entry from Genetic Analysis Software) | gene, genetic, genomic, r, any with r installation, bio.tools |
is listed by: Genetic Analysis Software is listed by: bio.tools is listed by: Debian |
nlx_154577, biotools:romprev | https://bio.tools/romprev | SCR_009361 | Regression of Offspring on Mid-Parent (REVised) | 2026-02-14 02:07:13 | 0 | |||||||
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PASS PEDIGREE Resource Report Resource Website |
PASS PEDIGREE (RRID:SCR_009315) | PASS PEDIGREE | software resource, software application | Software application to draw the most complex family trees in a matter of minutes instead of hours of work. The basis of this is an algorithm for automatically builing a family tree. Of course, manual adjustments in the family tree can be made for your specific requirements. PASS Pedigree meets all international conventions concerning the drawing of pedigrees. A converter can convert historical Cyrillic pedigrees automatically to PASS Pedigree. Unlike before, all your family trees are stored in one single database. PASS Pedigree can intelligently connect to many genetic centers (e.g. three genetic centers in the Netherlands) with the existing patient information, via the lab system HELIX based on HL7 techniques. (entry from Genetic Analysis Software) | gene, genetic, genomic | is listed by: Genetic Analysis Software | nlx_154509 | SCR_009315 | 2026-02-14 02:07:12 | 0 | |||||||||
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OSIRIS Resource Report Resource Website 100+ mentions |
OSIRIS (RRID:SCR_009313) | OSIRIS | software resource, software application | Software tool for the retrieval of articles from MEDLINE related to the sequence variants reported for a human gene. The variations considered are single nucleotide polymorphisms (SNPs), insertion/deletion polymorphisms (indel), microsatellite, and named variations (e.g. Alu sequences). (entry from Genetic Analysis Software), THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025. | gene, genetic, genomic | is listed by: Genetic Analysis Software | THIS RESOURCE IS NO LONGER IN SERVICE | nlx_154505 | SCR_009313 | 2026-02-14 02:07:18 | 218 | ||||||||
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P ACT Resource Report Resource Website 1+ mentions |
P ACT (RRID:SCR_009314) | P_ACT | software resource, software application | An R program that adjusts sets of up to 1000 p-values from association tests between correlated traits and SNPs for multiple testing, accounting for the correlation between tests. (entry from Genetic Analysis Software) | gene, genetic, genomic | is listed by: Genetic Analysis Software | nlx_154506 | SCR_009314 | P-values: Adjustment for Correlated Tests | 2026-02-14 02:06:49 | 4 | ||||||||
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NOCOM Resource Report Resource Website 1+ mentions |
NOCOM (RRID:SCR_009310) | NOCOM | software resource, software application | Software application to estimate parameters for mixture of normal distributions (entry from Genetic Analysis Software) | gene, genetic, genomic, fortran, ms-dos, os2 | is listed by: Genetic Analysis Software | nlx_154500 | SCR_009310 | 2026-02-14 02:07:12 | 8 | |||||||||
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SMOOTH Resource Report Resource Website 50+ mentions |
SMOOTH (RRID:SCR_009398) | software resource, software application | Software tool that recognises and removes the most unrealistic data pointsfor the construction of accurate linkage maps, which is not so much depending on the quality of the mapping software, but mostly on the marker data quality. Missing values and scoring errors can severely influence the calculated marker order. This software was used to construct the 10,000 marker potato map. The removal of improbable data point is a good medicine for linkage maps, that is not easily overdosed. One error is more harmfull than ten missing values. The software was never intended as user-friendly software. In these days it would be more useful to re-do the programming of the pascal source code into a perl script. Anyone who takes the initiative to generate such a script is welcomed to contact the authors. SMOOTH works best in close cooperation with mapping algorithm RECORD (entry from Genetic Analysis Software) | gene, genetic, genomic, pascal, ms-dos | is listed by: Genetic Analysis Software | nlx_154636 | http://www.plantbreeding.wur.nl/UK/software_smooth.html | SCR_009398 | 2026-02-14 02:07:14 | 57 | |||||||||
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SIMULATE Resource Report Resource Website 10+ mentions |
SIMULATE (RRID:SCR_009391) | software resource, software application | Software program to simulate genotypes in family members for a map of linked markers unlinked to a given affection status locus. the output is ready for analysis with UNKNOWN, ISIM, LSIM, or MSIM of the SLINK package. (entry from Genetic Analysis Software) | gene, genetic, genomic, pascal, ms-dos, vms, unix, bio.tools |
is listed by: Genetic Analysis Software is listed by: bio.tools is listed by: Debian |
nlx_154630, biotools:simulate | https://bio.tools/simulate | SCR_009391 | 2026-02-14 02:07:19 | 11 | |||||||||
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SIMUPOP Resource Report Resource Website 10+ mentions |
SIMUPOP (RRID:SCR_009392) | software resource, software application | A forward-based population genetics simulation program capable of simulating very complex evolution processes on large (think of millions) populations. Major features include variable population size; many built-in and hybrid (write in python) mutation, migration, selection models. simuPOP can be extended in Python so there is no limit on what you can do with it. (entry from Genetic Analysis Software) | gene, genetic, genomic, c++, (provided as python libraries) | is listed by: Genetic Analysis Software | nlx_154631 | https://pypi.python.org/pypi/simuPOP | http://bp6.stat.rice.edu:8080/simuPOP/ | SCR_009392 | 2026-02-14 02:06:51 | 26 | ||||||||
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MULTISIM Resource Report Resource Website 10+ mentions |
MULTISIM (RRID:SCR_009308) | MULTISIM | software resource, software application | Software application to analyze the numbers of individuals that founded new populations following a bottleneck or founding event (entry from Genetic Analysis Software) | gene, genetic, genomic, ms-dos | is listed by: Genetic Analysis Software | nlx_154498 | SCR_009308 | 2026-02-14 02:07:17 | 12 | |||||||||
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SAGE Resource Report Resource Website 1000+ mentions |
SAGE (RRID:SCR_009302) | SAGE | software resource, software application | Software application that provides researchers with the tools necessary for various types of statistical genetic analysis of human family data. (entry from Genetic Analysis Software) | gene, genetic, genomic, c, version 4.0 will be in c++, unix, (dec unix/solaris), ms-windows, (95/nt), linux |
is listed by: Genetic Analysis Software is listed by: SoftCite |
nlx_154606 | SCR_009302 | Statistical Analysis for Genetic Epidemiology | 2026-02-14 02:07:12 | 1029 | ||||||||
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PEDMANAGER Resource Report Resource Website |
PEDMANAGER (RRID:SCR_009300) | PEDMANAGER | software resource, software application | Software application (entry from Genetic Analysis Software) | gene, genetic, genomic, c, unix | is listed by: Genetic Analysis Software | nlx_154491 | SCR_009300 | 2026-02-14 02:06:49 | 0 | |||||||||
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SIMPLE Resource Report Resource Website 100+ mentions |
SIMPLE (RRID:SCR_009389) | software resource, software application | Software application that calculates linkage statistics, such as lod scores and NPL statistics by Sequential Imputation. (entry from Genetic Analysis Software) | gene, genetic, genomic, c, unix, solaris | is listed by: Genetic Analysis Software | nlx_154628 | SCR_009389 | Sequential Imputation for MultiPoint Linkage Estimation | 2026-02-14 02:07:14 | 417 | |||||||||
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SIMLINK Resource Report Resource Website 1+ mentions |
SIMLINK (RRID:SCR_009387) | software resource, software application | Software program to estimate the probability (power) of detecting linkage given family history information on a set of identified pedigrees. (entry from Genetic Analysis Software) | gene, genetic, genomic, fortran, ms-dos, unix, sunos, vms | is listed by: Genetic Analysis Software | nlx_154625 | SCR_009387 | 2026-02-14 02:07:19 | 3 | ||||||||||
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SIMLA Resource Report Resource Website 1+ mentions |
SIMLA (RRID:SCR_009385) | software resource, software application | SIMulation program that generates data sets of families for use in Linkage and Association studies. It allows the user flexibility in specifying marker and disease placement, locus heterogeneity, disequilibrium between markers and between markers and disease loci. Output is in the form of a LINKAGE pedigree file and is easily utilized, either directly or with minimal reformatting, as input for various genetic analysis packages (entry from Genetic Analysis Software) | gene, genetic, genomic, c++, unix, solaris, linux | is listed by: Genetic Analysis Software | nlx_154623 | http://wwwchg.duhs.duke.edu/software/simla.html | SCR_009385 | SIMulation of pedigree data for Linkage and Association studies | 2026-02-14 02:07:13 | 1 | ||||||||
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SILCLOD Resource Report Resource Website |
SILCLOD (RRID:SCR_009383) | software resource, software application | Software application to calculate nominal significance levels and critical LOD scores depending on the length of the investigated region, number of chromosomes, and the cross-over rate. The global significance level as well as the precision of the calculation have to be specified. (entry from Genetic Analysis Software) | gene, genetic, genomic | is listed by: Genetic Analysis Software | nlx_154619 | http://www.imbs.uni-luebeck.de/pub/silcLOD/index.html | SCR_009383 | SIgnificance Levels and Critical LODs | 2026-02-14 02:07:19 | 0 | ||||||||
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SIBERROR Resource Report Resource Website |
SIBERROR (RRID:SCR_009380) | software resource, software application | Software application that identifies pedigree errors in sibship data. Examples include half siblings, unrelated individuals, identical twins, and parental exclusions. The test statistic is based on the summation of the number of alleles shared by a pair of relatives for a large number of markers and the number of alleles and allele frequencies for those markers. (entry from Genetic Analysis Software) | gene, genetic, genomic, c, unix | is listed by: Genetic Analysis Software | nlx_154615 | SCR_009380 | SibError | 2026-02-14 02:06:51 | 0 | |||||||||
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TAGGER Resource Report Resource Website 50+ mentions |
TAGGER (RRID:SCR_009419) | software resource, software application | Software application (entry from Genetic Analysis Software) | gene, genetic, genomic, web-based |
is listed by: Genetic Analysis Software is listed by: SoftCite |
nlx_154669 | SCR_009419 | 2026-02-14 02:07:08 | 91 | ||||||||||
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SPLINK Resource Report Resource Website 10+ mentions |
SPLINK (RRID:SCR_009414) | software resource, software application | Software application for linkage analysis using affected sib pairs (entry from Genetic Analysis Software) | gene, genetic, genomic, c++, unix, sunos, ms-dos | is listed by: Genetic Analysis Software | nlx_154659 | http://www-gene.cimr.cam.ac.uk/clayton/software/ | SCR_009414 | affected Sib Pairs LINKage analysis | 2026-02-14 02:07:14 | 46 | ||||||||
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SSAHASNP Resource Report Resource Website 1+ mentions |
SSAHASNP (RRID:SCR_009415) | SSAHASNP | software resource, software application | A polymorphism detection tool that detects homozygous SNPs and indels by aligning shotgun reads to the finished genome sequence. Highly repetitive elements are filtered out by ignoring those kmer words with high occurrence numbers. For those less repetitive or non-repetitive reads, we place them uniquely on the reference genome sequence and find the best alignment according to the pair-wise alignment score if there are multiple seeded regions. From the best alignment, SNP candidates are screened, taking into account the quality value of the bases with variation as well as the quality values in the neighbouring bases, using neighbourhood quality standard (NQS). For insertions/deletions, we check if the same indel is mapped by more than one read, ensuring the detected indel with high confidence. (entry from Genetic Analysis Software) | gene, genetic, genomic | is listed by: Genetic Analysis Software | nlx_154661 | SCR_009415 | Sequence Search and Alignment by Hashing Algorithm for SNP detection | 2026-02-14 02:07:07 | 4 |
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