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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.
| Resource Name | Proper Citation | Abbreviations | Resource Type |
Description |
Keywords | Resource Relationships | |||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
AbbVie Resource Report Resource Website 500+ mentions |
AbbVie (RRID:SCR_010484) | ABBV | commercial organization | A research-based biopharmaceutical company that develops advanced therapies to address global health problems. | pharmaceutical, advanced therapy, biopharmaceutical, research, global health, commercial organization |
is related to: Kidney Health Initiative is related to: Structural Genomics Consortium is related to: Alzheimers Association Research Roundtable is related to: Abbott is related to: Abbott is related to: NEWMEDS is related to: ORBITO is related to: PREDECT |
nlx_158067, grid.472726.2 | https://ror.org/024e28c54 | SCR_010484 | AbbVie Inc., AbbVie Deutschland GmbH & Co KG, AbbVie Deutschland GmbH and Co KG | 2026-09-12 12:57:20 | 916 | |||||||
|
HMCan Resource Report Resource Website 10+ mentions |
HMCan (RRID:SCR_010858) | HMCan | software resource | A Hidden Markov Model based software tool that is developed to detect histone modification in cancer ChIP-seq data. | bio.tools |
is listed by: OMICtools is listed by: Debian is listed by: bio.tools has parent organization: King Abdullah University of Science and Technology; Makkah Province; Saudi Arabia |
PMID:24021381 | biotools:hmcan, OMICS_00443 | https://bio.tools/hmcan | SCR_010858 | Histone Modification in Cancer | 2026-09-12 12:57:24 | 14 | ||||||
|
DFLAT Resource Report Resource Website 1+ mentions |
DFLAT (RRID:SCR_010738) | DFLAT | data or information resource, data set, narrative resource, standard specification | We are an interdisciplinary team dedicated to annotating gene function related to human fetal development. We are contributing new functional annotation to the Gene Ontology, curating and mining gene sets suitable for the interpretation of developmental genomic data, and creating the computational tools needed to apply genomics for better understanding the molecular mechanisms of human development. Our GO annotation is in the process of being incorporated into the GOA public release. The GONE (Gene Ontology Non-Eligible) database is where we store annotations relevant to our research but that don''t quite meet GOA''s standards. Usually an annotation falls into this category because either the gene/protein described is a family of genes/proteins rather than a specific one, there is no UniProt ID to identify the gene/protein in the system, a GO term does not yet exist to describe the particular function, process, or location of the gene/protein, the species is not clearly identifiable in the paper, or the evidence is not as reliable (GO evidence codes TAS and NAS). As individual annotations these are more suspect than current GO annotation. However, for functional analysis of expression data, these gene sets can be valuable even with a certain amount of noise. We also include here a link to the supplementary data from our forthcoming PSB 2011 paper on gene set mining. | human, fetal, development | has parent organization: Tufts University; Massachusetts; USA | NICHD R01 HD058880 | PMID:21121032 | nlx_95610 | SCR_010738 | Developmental FunctionaL Annotation at Tufts | 2026-09-12 12:57:22 | 2 | ||||||
|
TESS: Transcription Element Search System Resource Report Resource Website 100+ mentions |
TESS: Transcription Element Search System (RRID:SCR_010739) | TESS | analysis service resource, data analysis service, data or information resource, database, production service resource, service resource | TESS is a web tool for predicting transcription factor binding sites in DNA sequences. It can identify binding sites using site or consensus strings and positional weight matrices from the TRANSFAC, JASPAR, IMD, and our CBIL-GibbsMat database. You can use TESS to search a few of your own sequences or for user-defined CRMs genome-wide near genes throughout genomes of interest. Search for CRMs Genome-wide: TESS now has the ability to search whole genomes for user defined CRMs. Try a search in the AnGEL CRM Searches section of the navigation bar.. You can search for combinations of consensus site sequences and/or PWMs from TRANSFAC or JASPAR. Search DNA for Binding Sites: TESS also lets you search through your own sequence for TFBS. You can include your own site or consensus strings and/or weight matrices in the search. Use the Combined Search under ''Site Searches'' in the menu or use the box for a quick search. TESS assigns a TESS job number to all sequence search jobs. The job results are stored on our server for a period of time specified in the search submit form. During this time you may recall the search results using the form on this page. TESS can also email results to you as a tab-delimited file suitable for loading into a spreadsheet program. Query for Transcription Factor Info: TESS also has data browsing and querying capabilities to help you learn about the factors that were predicted to bind to your sequence. Use the Query TRANSFAC or Query Matrices links above or use the search interface provided from the home page. | transcription factor, dna sequence, genome, promoter, gene regulation, FASEB list | has parent organization: University of Pennsylvania; Philadelphia; USA | PMID:18428685 | nlx_97404 | http://www.pcbi.upenn.edu/tess | SCR_010739 | Transcription Element Search System | 2026-09-12 12:57:22 | 191 | ||||||
|
miRTar Resource Report Resource Website 50+ mentions |
miRTar (RRID:SCR_010851) | miRTar | analysis service resource, data analysis service, data or information resource, data set, production service resource, service resource | An integrated web server for identifying miRNA-target interactions in human. The tool enables biologists easily to identify the biological functions and regulatory relationships between a group of known/putative miRNAs and protein coding genes. It also provides perspective of information on the miRNA targets on alternatively spliced transcripts. |
is listed by: OMICtools has parent organization: National Chiao Tung University; Hsinchu; Taiwan |
OMICS_00410 | SCR_010851 | MicroRNA Target prediction | 2026-09-12 12:57:24 | 55 | |||||||||
|
COPS Resource Report Resource Website 100+ mentions |
COPS (RRID:SCR_010852) | COPS | software resource | Software for detecting Co-Occurrence and Spatial Arrangement of Transcription Factor Binding Motifs in Genome-Wide Datasets. |
is listed by: OMICtools has parent organization: Heidelberg University; Baden-Wurttemberg; Germany |
PMID:23272209 | OMICS_00479 | SCR_010852 | COPS: Detecting Co-Occurrence and Spatial Arrangement of Transcription Factor Binding Motifs in Genome-Wide Datasets | 2026-09-12 12:57:24 | 273 | ||||||||
|
E-RANGE Resource Report Resource Website |
E-RANGE (RRID:SCR_010856) | E-RANGE | software resource | A Python package for doing RNA-seq and ChIP-seq (hence the dual-use). | is listed by: OMICtools | OMICS_00439 | SCR_010856 | 2026-09-12 12:57:24 | 0 | ||||||||||
|
SRS Resource Report Resource Website 1+ mentions |
SRS (RRID:SCR_010736) | SRS | analysis service resource, data analysis service, data or information resource, database, production service resource, service resource | THIS RESOURCE IS NO LONGER IN SERVICE, documented August 29, 2016. The EBI SRS server is a primary gateway to major databases in the field of molecular biology produced and supported at EBI as well as European public access point to the MEDLINE database provided by US National Library of Medicine (NLM). It is a reference server for latest developments in data and application integration. Features include: concept of virtual databases, integration of XML databases like the Integrated Resource of Protein Domains and Functional Sites (InterPro), Gene Ontology (GO), MEDLINE, Metabolic pathways, etc., user friendly data representation in ''Nice views'', SRSQuickSearch bookmarklets. Quick Searches allow users to make a number of searches without needing to learn how to use SRS in depth. The searches query some of the common databanks without having to go and select them explicitly and without the need to understand the SRS Query Forms. Quick Searches can be performed from either the Start page (when you first open SRS) or the SRS Quick Search page (when you are already in a project). SRS also has the ability to search for links between your current results and related information in other databanks. Additionally, it is able to analyze the results of your search using many bioinformatics analysis tools or applications. This enables you to seek out further information that may be relevant to your initial search. | data set, gold standard |
is listed by: 3DVC has parent organization: European Bioinformatics Institute |
PMID:11847095 PMID:12176845 PMID:8435768 |
THIS RESOURCE IS NO LONGER IN SERVICE | nlx_95251 | SCR_010736 | EBI SRS, EBI SRS server, Sequence Retrieval System | 2026-09-12 12:57:22 | 1 | ||||||
|
FindPeaks Resource Report Resource Website 100+ mentions |
FindPeaks (RRID:SCR_010857) | FindPeaks | software resource | Software application that can be used for converting Eland, Maq (.map), BED or other files into WIG files and identifying areas of enrichment (ChIP-Seq analysis). | chip-seq |
is listed by: OMICtools has parent organization: SourceForge |
BC Cancer Agency ; Michael Smith Foundation for Health Research |
OMICS_00440 | SCR_010857 | 2026-09-12 12:57:24 | 348 | ||||||||
|
CoRAL - Classification of RNAs by Analysis of Length Resource Report Resource Website 10+ mentions |
CoRAL - Classification of RNAs by Analysis of Length (RRID:SCR_010828) | CoRAL | software resource | A machine learning software package that can predict the precursor class of small RNAs present in a high-throughput RNA-sequencing dataset. In addition to classification, it also produces information about the features that are most important for discriminating different populations of small non-coding RNAs. |
is listed by: OMICtools has parent organization: University of Pennsylvania; Philadelphia; USA |
PMID:23700308 | Acknowledgement requested | OMICS_00372 | SCR_010828 | Classification of RNAs by Analysis of Length | 2026-09-12 12:57:24 | 11 | |||||||
|
PriVar Resource Report Resource Website 1+ mentions |
PriVar (RRID:SCR_010784) | PriVar | software resource | A toolkit for prioritizing SNVs and indels from next-generation sequencing data. | is listed by: OMICtools | OMICS_00160 | SCR_010784 | 2026-09-12 12:57:23 | 2 | ||||||||||
|
CNVer Resource Report Resource Website 1+ mentions |
CNVer (RRID:SCR_010820) | CNVer | software resource | A method for CNV detection that supplements the depth-of-coverage with paired-end mapping information, where matepairs mapping discordantly to the reference serve to indicate the presence of variation. | bio.tools |
is listed by: OMICtools is listed by: bio.tools is listed by: Debian |
biotools:cnver, OMICS_00341 | https://bio.tools/cnver | SCR_010820 | 2026-09-12 12:57:24 | 8 | ||||||||
|
CNVnator Resource Report Resource Website 500+ mentions |
CNVnator (RRID:SCR_010821) | CNVnator | software resource | An approach to discover, genotype, and characterize typical and atypical CNVs from family and population genome sequencing. | is listed by: OMICtools | OMICS_00343 | SCR_010821 | 2026-09-12 12:57:24 | 547 | ||||||||||
|
Diplotyper Resource Report Resource Website |
Diplotyper (RRID:SCR_010789) | Diplotyper | software resource | A fully automated software tool which is available for Linux to investigate associations between a diplotype group and a phenotype in linear or logistic regression. |
is listed by: OMICtools has parent organization: Google Code |
OMICS_00195 | SCR_010789 | 2026-09-12 12:57:23 | 0 | ||||||||||
|
Control-FREEC Resource Report Resource Website 100+ mentions |
Control-FREEC (RRID:SCR_010822) | Control-FREEC | software resource | Prediction of copy number alterations and loss of heterozygosity using deep-sequencing data. | is listed by: OMICtools | OMICS_00344 | SCR_010822 | 2026-09-12 12:57:24 | 346 | ||||||||||
|
readDepth Resource Report Resource Website 10+ mentions |
readDepth (RRID:SCR_010824) | readDepth | software resource | This package for R can detect copy number aberrations by measuring the depth of coverage obtained by massively parallel sequencing of the genome. | is listed by: OMICtools | OMICS_00350 | SCR_010824 | 2026-09-12 12:57:24 | 23 | ||||||||||
|
HapCUT Resource Report Resource Website 10+ mentions |
HapCUT (RRID:SCR_010791) | HapCUT | software resource | A max-cut based algorithm for haplotype assembly using sequence reads from the two chromosomes of an individual. | is listed by: OMICtools | OMICS_00198 | SCR_010791 | 2026-09-12 12:57:23 | 17 | ||||||||||
|
Relate Resource Report Resource Website 10+ mentions |
Relate (RRID:SCR_010794) | Relate | software resource | Software providing a method that estimates the probability of sharing alleles identity by descent (IBD) across the genome and can also be used for mapping disease loci using distantly related individuals. | bio.tools |
is listed by: OMICtools is listed by: bio.tools is listed by: Debian |
PMID:19025785 | biotools:relateadmix, OMICS_00207 | https://bio.tools/relateadmix | SCR_010794 | 2026-09-12 12:57:23 | 47 | |||||||
|
National Institute of Genetics; Shizuoka; Japan Resource Report Resource Website |
National Institute of Genetics; Shizuoka; Japan (RRID:SCR_010836) | institution | Institute for genetics, through National BioResource Project, collects, preserves, and provides bio-resources (strains, populations, tissues, cells, genes of animals, plants and microorganisms, and information on these materials for R&D use) that are essential for life science research. | RIN, Resource Information Network, strains, populations, tissues, cells, genes of animals, plants and microorganisms, RRID Community Authority |
is listed by: Resource Information Network is parent organization of: Genome Network Platform is parent organization of: DNA DataBank of Japan (DDBJ) is parent organization of: NEXTDB is parent organization of: RAP-DB is parent organization of: Alternate Splicing - induced ALteration of Protein Structure is parent organization of: GTOP - Genomes To Protein structures is parent organization of: Protein Mutant Database works with: International Mouse Strain Resource |
nlx_92390 | SCR_010836 | NIG | 2026-09-12 12:57:24 | 0 | |||||||||
|
RNAsnp Resource Report Resource Website 10+ mentions |
RNAsnp (RRID:SCR_010837) | RNAsnp | analysis service resource, data analysis service, production service resource, service resource, software resource | Software / Web Server to predict the effect of SNPs on local RNA secondary structure based on the RNA folding algorithms implemented in the Vienna RNA package. |
is listed by: OMICtools has parent organization: University of Copenhagen; Copenhagen; Denmark |
PMID:23630321 | OMICS_00392 | SCR_010837 | RNAsnp Web Server, RNAsnp Web Server: Predicting SNP effects on local RNA secondary structure | 2026-09-12 12:57:24 | 34 |
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