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http://www.detaibio.com/sms2/protein_gravy.html

Web protein hydrophilicity analysis tool.

Proper citation: protein hydrophilicity analysis tool (RRID:SCR_023015) Copy   

•   Source: SciCrunch Registry

http://www.intego.be

Computerized morbidity registration network in Belgium based on general practice data.Contains demographic, clinical, biomedical, and prescription data, registered with computer generated keywords in electronic health record.

Proper citation: Intego (RRID:SCR_022563) Copy   

•   Source: SciCrunch Registry

https://atlas.kpmp.org/

Atlas is set of interactive tools built to promote retrieval, exploration, discovery, and analysis of Kidney Precision Medicine Project data by greater research community. Datasets available in repository are combination of raw and processed data from KPMP participant biopsies and reference tissue samples.

Proper citation: Kidney Tissue Atlas (RRID:SCR_021626) Copy   

•   Source: SciCrunch Registry

https://www.scopus.com/

Abstract and indexing database with full text links that is produced by Elsevier Co. Combines expertly curated abstract and citation database with enriched data and linked scholarly literature across wide variety of disciplines.

Proper citation: Scopus (RRID:SCR_022559) Copy   

•   Source: SciCrunch Registry

https://docs.google.com/presentation/d/13KqqDOFLbhCPRsCqf4zETdcjhZECIXD_/edit#slide=id.p1

MJFF in partnership with Aligning Science Across Parkinson’s are in the process of establishing data platform, CRN Cloud, leveraging Verily Workbench to share data generated by researcher labs funded through ASAP Collaborative Research Network. The data types include mainly raw and processed single cell RNA-seq, single nucleus RNA-seq, and bulk RNA-seq from both PD and healthy control samples.

Proper citation: Collaborative Research Network Cloud (RRID:SCR_023923) Copy   

•   Source: SciCrunch Registry

https://ratgenes.org/C-gord/

Center maintains database containing all phenotypical data collected by Research Projects and Ancillary collaborators, as well as RNAseq and genotype data.Provides access to data generated by NIDA center for genetic studies of drug abuse in outbred rats and additional research projects that use N/NIH heterogeneous stock (HS) outbred rats and Center’s core services that support genotyping and analysis.Alignes data generated in HS rats with FAIR (Findable, Accessible, Interoperative, Reusable) data management principles.Provides structured access to data associated with research papers produced by research projects that use HS rats.

Proper citation: C-GORD (RRID:SCR_021866) Copy   

•   Source: SciCrunch Registry

https://adastra.autosome.ru/zanthar

Landscape of allele specific transcription factor binding in human genome. Creators conducted meta analysis of ChIP-Seq experiments and assembled database of allele specific binding events listing more than half million entries at nearly 270 thousand single nucleotide polymorphisms for several hundred human transcription factors and cell types.

Proper citation: Allelic Dosage corrected Allele Specific human Transcription factor binding sites (RRID:SCR_021863) Copy   

•   Source: SciCrunch Registry

https://tabula-sapiens-portal.ds.czbiohub.org/

Single cell transcriptomic atlas of multiple organs from individual human donors. Multiple organ, single cell transcriptomic atlas of humans. Molecular reference atlas for cell types of human body. Provides molecular definition of these cell types and reveals many other aspects of human biology, including how same gene can be spliced differently in different cell types, how shared cell types in different tissues can have subtle differences in their identities, and how clones of immune system can be shared across tissues.

Proper citation: Tabula Sapiens (RRID:SCR_022314) Copy   

•   Source: SciCrunch Registry

https://www.mongodb.com/

General purpose, document based, distributed database built for modern application developers and for the cloud. Offers Community and Enterprise version of database.MongoDB Community is source available and free to use edition of MongoDB. MongoDB Enterprise is available as part of MongoDB Enterprise Advanced subscription and includes comprehensive support for your MongoDB deployment. MongoDB Enterprise also adds enterprise-focused features such as LDAP and Kerberos support, on-disk encryption, and auditing.MongoDB also offers Atlas,hosted MongoDB Enterprise service option in cloud which requires no installation overhead and offers free tier to get started.

Proper citation: MongoDB (RRID:SCR_021224) Copy   

•   Source: SciCrunch Registry

https://www.grnpedia.org/trrust/

TRUSST is reference database of human transcriptional regulatory interactions.TRRUST v2 is manually curated expanded reference database of human and mouse transcriptional regulatory interactions.

Proper citation: Transcriptional Regulatory Relationships Unrevealed by Sentence based Text mining database (RRID:SCR_022554) Copy   

•   Source: SciCrunch Registry

https://www.grnpedia.org/trrust/Network_search_form.php

Reference database of human transcriptional regulatory interactions. Manually curated database of human and mouse transcriptional regulatory networks.

Proper citation: TTRUST (RRID:SCR_022490) Copy   

•   Source: SciCrunch Registry

https://www.fli.de/en/institutes/department-of-experimental-animal-facilities-and-biorisk-management-atb/bio-bank/#:~:text=Collection%20of%20Cell%20Lines%20in%20Veterinary%20Medicine%20(CCLV),the%20collection%20comprises%201%2C500%20lines.

Generates, characterises and collects cell lines which are of interest for veterinary research and diagnostics. Collection includes cell lines of farm animals such as cattle, pig, horse, sheep, goat and poultry and other mammals, birds, reptiles, fishes and insects (70 species).Authentication and quality-control tests (tests for contamination with mycoplasms, bacteria, BVDV) of the cultures are done routinely.Cell cultures are provided to scientists of the Friedrich-Loeffler-Institute and other non-commercial institutions worldwide after consultation of a scientific staff member of the CCLV.

Proper citation: Collection of Cell Lines in Veterinary Medicine (RRID:SCR_023182) Copy   

•   Source: SciCrunch Registry

http://isyslab.info/NeuroPep/

Comprehensive resource of neuropeptides, which holds non-redundant neuropeptide entries. Data collected from resources including MEDLINE abstracts, full papers, UniProt,database at www.neuropeptides.nl and Neuropedia. Contains detailed annotations for each entry, including source organisms, tissue specificity, families, names, post-translational modifications, 3D structures and literature references. Amino acid compositions, isoelectric points, molecular weight and other physicochemical properties of peptides are also provided. Search database with keywords such as sequence, name, family, etc.,User friendly web tools like browsing, sequence alignment and mapping are also integrated.Users can submit new entries online. Each new entry is validated before incorporating it.

Proper citation: NeuroPep (RRID:SCR_023102) Copy   

•   Source: SciCrunch Registry

http://www.timetree.org

Public knowledge base for information on evolutionary timescale of life. Data from thousands of published studies are assembled into searchable tree of life scaled to time.

Proper citation: TimeTree (RRID:SCR_021162) Copy   

•   Source: SciCrunch Registry

http://opig.stats.ox.ac.uk/webapps/newsabdab/sabdab/

Database containing all antibody structures available in the PDB, annotated and presented in consistent fashion.Each structure is annotated with number of properties including experimental details, antibody nomenclature (e.g. heavy-light pairings), curated affinity data and sequence annotations. You can use the database to inspect individual structures, create and download datasets for analysis, search the database for structures with similar sequences to your query, monitor the known structural repetoire of antibodies.

Proper citation: Structural Antibody Database (RRID:SCR_022096) Copy   

•   Source: SciCrunch Registry

http://exon.cshl.org/cgi-bin/atprobe/atprobe.pl

Arabidopsis thaliana promoter binding element database that focuses on specific binding elements on known genes, found with experimental methods.

Proper citation: AtProbe (RRID:SCR_005412) Copy   

•   Source: SciCrunch Registry

http://cgi-www.daimi.au.dk/cgi-chili/datfap/frontdoor.py

A database of transcription factors from 13 plant species, and PCR primers for around 90% of them.

Proper citation: DATFAP (RRID:SCR_005413) Copy   

•   Source: SciCrunch Registry

http://bioinfozen.uncc.edu/tfindit/

A database and web service for structural bioinformatics studies of transcription factor (TF)-DNA interactions. Various datasets can be generated based on one or more search options specified by users.

Proper citation: TFinDIT (RRID:SCR_005411) Copy   

•   Source: SciCrunch Registry

http://www.phenologs.org/

Database for identifying orthologous phenotypes (phenologs). Mapping between genotype and phenotype is often non-obvious, complicating prediction of genes underlying specific phenotypes. This problem can be addressed through comparative analyses of phenotypes. We define phenologs based upon overlapping sets of orthologous genes associated with each phenotype. Comparisons of >189,000 human, mouse, yeast, and worm gene-phenotype associations reveal many significant phenologs, including novel non-obvious human disease models. For example, phenologs suggest a yeast model for mammalian angiogenesis defects and an invertebrate model for vertebrate neural tube birth defects. Phenologs thus create a rich framework for comparing mutational phenotypes, identify adaptive reuse of gene systems, and suggest new disease genes. To search for phenologs, go to the basic search page and enter a list of genes in the box provided, using Entrez gene identifiers for mouse/human genes, locus ids for yeast (e.g., YHR200W), or sequence names for worm (e.g., B0205.3). It is expected that this list of genes will all be associated with a particular system, trait, mutational phenotype, or disease. The search will return all identified model organism/human mutational phenotypes that show any overlap with the input set of the genes, ranked according to their hypergeometric probability scores. Clicking on a particular phenolog will result in a list of genes associated with the phenotype, from which potential new candidate genes can identified. Currently known phenotypes in the database are available from the link labeled ''Find phenotypes'', where the associated gene can be submitted as queries, or alternately, can be searched directly from the link provided.

Proper citation: Phenologs (RRID:SCR_005529) Copy   

•   Source: SciCrunch Registry

http://blog.ketyov.com/

Bradley Voytek''''s blog is where he tries out new ideas. He will often be wrong, but that''''s the point. He is a Neuroscientist studying human cognition, neuroplasticity, and brain computer interfacing. Into really geeky stuff. World zombie neuroscience expert. Also runs brainSCANr.com with his wife, Jessica.

Proper citation: Oscillatory Thoughts (RRID:SCR_005481) Copy   

•   Source: SciCrunch Registry