Tools   Select Another Resource Report Type

http://meme-suite.org/tools/dreme

Software tool to discover short, ungapped motifs (recurring, fixed-length patterns) that are relatively enriched in sequences compared with shuffled sequences or control sequences (sample output from sequences).

Proper citation: DREME (RRID:SCR_016860) Copy   

•   Source: SciCrunch Registry

https://pregnancycolab.tghn.org/collect/

Collaborative database for pregnancy and placental research studies worldwide by Global Pregnancy Collaboration CoLab . Database for collecting data for pregnancy studies in preeclampsia and other fields. Database has web based data entry platform with study specific user access. Data can also be entered offline using formatted spreadsheet template that can be uploaded to database in bulk or stored locally. Data is property of investigator but with permission can be combined into larger studies across centers and countries. Collaboration is enabled but not required.

Proper citation: COLLECT database (RRID:SCR_018366) Copy   

•   Source: SciCrunch Registry

http://software.broadinstitute.org/gsea/msigdb/index.jsp

Collection of annotated gene sets for use with Gene Set Enrichment Analysis (GSEA) software.

Proper citation: Molecular Signatures Database (RRID:SCR_016863) Copy   

•   Source: SciCrunch Registry

https://www.hsrd.research.va.gov/for_researchers/cyber_seminars/archives/video_archive.cfm?SessionID=3814

Shared knowledgebase of VA EHR-based phenotype algorithms, definitions and data curation metadata.

Proper citation: VA Phenomics Library (RRID:SCR_019107) Copy   

•   Source: SciCrunch Registry

https://github.com/aertslab/SCENIC

Software R package as single cell regulatory network inference and clustering. Used for simultaneous gene regulatory network reconstruction and cell state identification from single cell RNA-seq data.

Proper citation: SCENIC (RRID:SCR_017247) Copy   

•   Source: SciCrunch Registry

https://it.uib.no/en/Safe

Platform for Secure Access to Research Data and E-Infrastructure based on European Standards for Health Case information. Used for secure processing of sensitive personal data in research in health and care sector.

Proper citation: Secure Access to Research Data and E-Infrastructure (RRID:SCR_017246) Copy   

•   Source: SciCrunch Registry

https://sciex.com/products/software/lipidview-software

Software tool for molecular characterization and quantification of lipid species from electrospray mass spectrometry data. Enables lipid profiling by searching parent and fragment ion masses against lipid fragment database and reports numerical and graphical output for various lipid molecular species, lipid classes, fatty acids, and long chain bases.

Proper citation: LipidView Software (RRID:SCR_017003) Copy   

•   Source: SciCrunch Registry

https://gitlab.com/KHanghoj/DamMet

Software tool as a full probabilistic model for mapping ancient methylomes using sequencing data underlying an ancient specimen.

Proper citation: DamMet (RRID:SCR_016959) Copy   

•   Source: SciCrunch Registry

https://osf.io/rmqaw/

Open source resources to execute stop signal task and analyze resulting data. Simulation code is provided, and can be used in planning stage for investigation of response inhibition and impuls control.

Proper citation: stop-signal task resources (RRID:SCR_017137) Copy   

•   Source: SciCrunch Registry

https://github.com/bids-standard/bids-validator

Software validation tool that checks submitted folder structure for compliance to BIDS data standard. Validates Brain Imaging Data Structure.

Proper citation: BIDS Validator (RRID:SCR_017255) Copy   

•   Source: SciCrunch Registry

https://hub.docker.com/r/mziemann/tallyup/

Docker image that is used to process all of the data present in the Digital Expression Explorer 2 dataset. It can be freely used by anyone to process data on NCBI SRA or process their own RNA-seq fastq files. Used for bulk reprocessing of public RNA-seq data from SRA. The pipeline tallies the reads assigned to each gene or transcript.

Proper citation: Digital Expression Explorer 2 Docker Image (RRID:SCR_016931) Copy   

•   Source: SciCrunch Registry

http://ophid.utoronto.ca/mirDIP/

microRNA data integration portal to find microRNAs that target a gene, or genes targeted by a microRNA, in Homo sapiens. Software to integrate prediction databases to elucidate accurate microRNA:target relationships. Used for human microRNA prediction studies.

Proper citation: mirDIP (RRID:SCR_016770) Copy   

•   Source: SciCrunch Registry

https://www.schrodinger.com/maestro

Software tool for all purpose molecular modeling environment. Maestro is the portal to all of Schrödinger's computational technology. Helps researchers organize and analyze data.

Proper citation: Maestro (RRID:SCR_016748) Copy   

•   Source: SciCrunch Registry

http://cab.spbu.ru/software/rnaquast/

Software tool for evaluating RNA-Seq assembly quality and benchmarking transcriptome assemblers using reference genome and gene database. Capable to estimate gene database coverage by raw reads and de novo quality assessment using third party software.

Proper citation: rnaQUAST (RRID:SCR_016994) Copy   

•   Source: SciCrunch Registry

http://www.nitrc.org/projects/brainlife_io/

Platform for publishing reproducible code and datasets and providing access to national supercomputers, private clouds, and institutional high-performance computer systems to promote open software and data sharing to advance understanding of the human brain.

Proper citation: brainlife.io (RRID:SCR_016513) Copy   

•   Source: SciCrunch Registry

https://github.com/ropenscilabs/datastorr

Software package for simple data retrieval and versioning.

Proper citation: datastorr (RRID:SCR_017040) Copy   

•   Source: SciCrunch Registry

https://openknowledgemaps.org/

Software tool as an open source knowledge mapping software that increases the visibility of research findings for science and society. Visual interface to the world's scientific knowledge.

Proper citation: Open Knowledge Maps (RRID:SCR_016470) Copy   

•   Source: SciCrunch Registry

https://www.ncbi.nlm.nih.gov/genbank/wgs/

Project for assemblies of incomplete genomes or incomplete chromosomes of prokaryotes or eukaryotes that are being sequenced by a whole genome shotgun strategy. WGS projects may be annotated, but annotation is not required. The nucleotide and protein data from all WGS projects go into the BLAST database.

Proper citation: Whole Genome Shotgun (WGS) Project (RRID:SCR_016637) Copy   

•   Source: SciCrunch Registry

https://www.ncbi.nlm.nih.gov/genbank/tbl2asn2/

Software tool as a command-line program that automates the creation of sequence records for submission to GenBank. Records need no additional manual editing before submission.

Proper citation: tbl2asn (RRID:SCR_016636) Copy   

•   Source: SciCrunch Registry

http://www.reproducibleimaging.org

Center to help neuroimaging researchers to find and share data in FAIR fashion, to describe their data and analysis workflows in replicable fashion, to manage their computational resource options so that outcomes of neuroimaging research are more reproducible.

Proper citation: ReproNim: A Center for Reproducible Neuroimaging Computation (RRID:SCR_016001) Copy   

•   Source: SciCrunch Registry