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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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On page 132 showing 2621 ~ 2640 out of 2,818 results
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  • RRID:SCR_010830

    This resource has 10+ mentions.

http://mimirna.centenary.org.au/mireval/

A web tool for simple microRNA prediction in genome sequences.

Proper citation: miREval (RRID:SCR_010830) Copy   


  • RRID:SCR_010799

    This resource has 1+ mentions.

http://phencode.bx.psu.edu/

A collaborative project to better understand the relationship between genotype and phenotype in humans that connects human phenotype and clinical data in various locus-specific mutation databases (LSDBs) with data on genome sequences, evolutionary history, and function in the UCSC Genome Browser. PhenCode is a collaboration among researchers at Penn State, UC Santa Cruz, and locus experts at other institutions.

Proper citation: PhenCode (RRID:SCR_010799) Copy   


  • RRID:SCR_010885

    This resource has 1+ mentions.

http://159.149.160.51/pscan_chip_dev/

Web server that, starting from a collection of genomic regions derived from a ChIP-Seq experiment, scans them using motif descriptors like JASPAR or TRANSFAC position-specific frequency matrices, or descriptors uploaded by users, and it evaluates both motif enrichment and positional bias within the regions according to different measures and criteria.

Proper citation: Pscan-ChIP (RRID:SCR_010885) Copy   


  • RRID:SCR_010800

    This resource has 1+ mentions.

http://www.unc.edu/~yunmli/1000G-imp/

A comprehensive SNP and indel imputability database.

Proper citation: SNP and indel Imputability (RRID:SCR_010800) Copy   


  • RRID:SCR_010773

    This resource has 50+ mentions.

http://cupsat.tu-bs.de/

A tool to predict changes in protein stability upon point mutations.

Proper citation: CUPSAT (RRID:SCR_010773) Copy   


  • RRID:SCR_010774

    This resource has 1+ mentions.

http://ls-snp.icm.jhu.edu/ls-snp-pdb/

A web tool for genome-wide annotation of human SNPs.

Proper citation: LS-SNP/PDB (RRID:SCR_010774) Copy   


  • RRID:SCR_010896

    This resource has 1+ mentions.

http://legumetfdb.psc.riken.jp/

A public database that provides predicted transcription factor (TF) encoding genes annotated in genome sequences of three major legume species: soybean (Glycine max), Lotus japonicus and Medicago truncatula.

Proper citation: LegumeTFDB (RRID:SCR_010896) Copy   


  • RRID:SCR_010776

    This resource has 50+ mentions.

http://bleoberis.bioc.cam.ac.uk/mcsm

Data analysis service to the study of missense mutations which relies on graph-based signatures.

Proper citation: mCSM (RRID:SCR_010776) Copy   


  • RRID:SCR_010898

    This resource has 10+ mentions.

http://plantgrn.noble.org/PlantTFcat/

A web-based analysis tool that is designed to identify and categorize plant TF/TR/CR genes from genome-scale protein and nucleic acid sequences by systematically analyzing InterProScan domain patterns in protein sequences., THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025.

Proper citation: PlantTFcat (RRID:SCR_010898) Copy   


  • RRID:SCR_010749

    This resource has 100+ mentions.

http://www.imgt.org/IMGT_vquest/share/textes/

Data analysis service for the standardized analysis of the immunoglobulin (IG) and T cell receptor (TR) rearranged nucleotide sequences. It identifies the variable (V), diversity (D) and joining (J) genes and alleles by alignment with the germline IG and TR gene and allele sequences of the IMGT reference directory. New functionalities were added through a complete rewrite in Java. IMGT/V-QUEST analyses batches of sequences (up to 50) in a single run. IMGT/V-QUEST describes the V-REGION mutations and identifies the hot spot positions in the closest germline V gene. IMGT/V-QUEST can detect insertions and deletions in the submitted sequences by reference to the IMGT unique numbering. IMGT/V-QUEST integrates IMGT/JunctionAnalysis for a detailed analysis of the V-J and V-D-J junctions, and IMGT/Automat for a full V-J- and V-D-J-REGION annotation. IMGT/V-QUEST displays, in ''Detailed view'', the results and alignments for each submitted sequence individually and, in ''Synthesis view'', the alignments of the sequences that, in a given run, express the same V gene and allele.

Proper citation: IMGT/V-QUEST (RRID:SCR_010749) Copy   


  • RRID:SCR_010901

    This resource has 1+ mentions.

http://treetfdb.bmep.riken.jp/index.pl

A public database that provides the complete transcription factor (TF) repertoires of 6 genome sequenced tree species: papaya (Carica papaya), jatoropha (Jatropha curcas), cassava (Manihot esculenta), poplar (Populus trichocarpa), castor bean (Ricinus communis) and grape vine (Vitis vinifera). from annotated genes on each genome.

Proper citation: TreeTFDB (RRID:SCR_010901) Copy   


  • RRID:SCR_010878

    This resource has 1+ mentions.

http://cmotifs.tchlab.org/

Data analysis service providing a motif discovery platform developed to help biologists to find novel as well as known motifs in their peak datasets from transcription factor (TF) binding experiments such as ChIP-seq and ChIP-chip.

Proper citation: CompleteMOTIFs (RRID:SCR_010878) Copy   


  • RRID:SCR_011818

    This resource has 1000+ mentions.

http://tcoffee.crg.cat/apps/tcoffee/do:regular

A multiple sequence alignment server which can align Protein, DNA and RNA sequences.

Proper citation: T-Coffee (RRID:SCR_011818) Copy   


  • RRID:SCR_011933

    This resource has 10+ mentions.

http://www.cbs.dtu.dk/services/HMMgene/

Data analysis service for prediction of vertebrate and C. elegans genes.

Proper citation: HMMgene (RRID:SCR_011933) Copy   


  • RRID:SCR_011813

    This resource has 100+ mentions.

http://probcons.stanford.edu/

Efficient protein multiple sequence alignment program, which has demonstrated a statistically significant improvement in accuracy compared to several leading alignment tools.

Proper citation: ProbCons (RRID:SCR_011813) Copy   


  • RRID:SCR_012117

    This resource has 100+ mentions.

http://genevenn.sourceforge.net/

A web application creating Venn diagrams from two or three gene lists.

Proper citation: GeneVenn (RRID:SCR_012117) Copy   


  • RRID:SCR_012755

http://blog.openhelix.eu/

Blog where you will find a genomics resources news portal with daily postings about genomics resources, genomics news and research, science and more.

Proper citation: OpenHelix Blog (RRID:SCR_012755) Copy   


  • RRID:SCR_012876

    This resource has 1+ mentions.

http://www.r-bloggers.com/

A central hub of content collected from bloggers who write about R (in English).

Proper citation: R-Bloggers.com (RRID:SCR_012876) Copy   


  • RRID:SCR_010975

    This resource has 1+ mentions.

https://bmcbioinformatics.biomedcentral.com/articles/10.1186/1471-2105-8-S1-S21

A microarray platform that uses the Illumina and Affymetrix GeneChip microarray technology for genome and transcriptome analyses and a web-based database that consists exclusively of high quality Affymetrix data from immunological experiments hosted by a public, non-profit consortium of three scientific public institutions aimed to develop, integrate and disseminate Functional Genomics.

Proper citation: Genopolis (RRID:SCR_010975) Copy   


  • RRID:SCR_011822

    This resource has 5000+ mentions.

http://blast.ncbi.nlm.nih.gov/Blast.cgi?PROGRAM=tblastn&PAGE_TYPE=BlastSearch&LINK_LOC=blasthome

Tool to search translated nucleotide databases using a protein query.

Proper citation: TBLASTN (RRID:SCR_011822) Copy   



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