Tools   Select Another Resource Report Type

https://github.com/ABCD-STUDY/redcap-importer

Software that automates the process of retrieving and converting data to the format of a RedCap table and allows selection of directories and files for import.

Proper citation: redcap-importer (RRID:SCR_016032) Copy   

•   Source: SciCrunch Registry

https://github.com/ABCD-STUDY/ABCDreport

Software application as a simple system to review study progress. Used in ABCD study.

Proper citation: ABCDreport (RRID:SCR_016030) Copy   

•   Source: SciCrunch Registry

http://www.sanger.ac.uk/science/tools/seqtools

Software for multiple sequence alignment viewing, editing and phylogeny. It includes a set of user-configurable modes to color residues used to create high-quality reference alignments.

Proper citation: Belvu (RRID:SCR_015989) Copy   

•   Source: SciCrunch Registry

https://github.com/sanger-pathogens/Bio-Tradis

Analysis software for the output from TraDIS (Transposon Directed Insertion Sequencing) analyses of dense transposon mutant libraries. The Bio-Tradis analysis pipeline is implemented as an extensible Perl library which can either be used as is, or as a basis for the development of more advanced analysis tools.

Proper citation: Bio-tradis (RRID:SCR_015993) Copy   

•   Source: SciCrunch Registry

http://m6asnp.renlab.org

Web server implemented in JAVA and PHP for annotating genetic variants by m6A function. It predicts and annotates N6-methyladenosine (m6A) alterations from genetic variants data such as germline SNPs or cancer somatic mutations. It employs two accurate prediction models for human and mouse using Random Forest algorithm. It conducts a statistical analysis for all the predicted m6A alterations. Provides statistical diagrams and a genome browser to visualize the topology characteristics of predicted m6A alterations.

Proper citation: m6ASNP: Annotation of genetic variants by m6A function (RRID:SCR_016048) Copy   

•   Source: SciCrunch Registry

https://imagen-europe.com/

Research project examining how biological, psychological, and environmental factors during adolescence may influence brain development and mental health. Using brain imaging and genetics, the project will help develop prevention strategies and improved therapies for mental health disorders in the future., THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025.

Proper citation: IMAGEN (RRID:SCR_016045) Copy   

•   Source: SciCrunch Registry

http://www.vicbioinformatics.com/software.barrnap.shtml

THIS RESOURCE IS NO LONGER IN SERVICE. Documented on February 28,2023. Software to predict the location of ribosomal RNA genes in genomes. It supports bacteria, archaea, mitochondria, and eukaryotes. It takes FASTA DNA sequence as input, writes GFF3 as output, and supports multithreading., THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025.

Proper citation: Barrnap (RRID:SCR_015995) Copy   

•   Source: SciCrunch Registry

http://ced.co.uk/products/power3

Data acquisition interface from Cambridge Electronic Design Limited. Works with Spike2 to provide continuous acquisition tasks. Records waveform data, digital and marker information, and can generate waveform and digital outputs simultaneously for real-time, multi-tasking experiment control.

Proper citation: CED: Power1401 (RRID:SCR_016040) Copy   

•   Source: SciCrunch Registry

http://itolab.med.kyushu-u.ac.jp/BMap/index.html

Software that maps whole-genome and targeted bisulfite sequence reads to reference genomes. It is especially useful for reads obtained using post-bisulfite adaptor tagging (PBAT)., THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025.

Proper citation: BMap (RRID:SCR_016044) Copy   

•   Source: SciCrunch Registry

https://www.nitrc.org/projects/normalizefov

FSoftware for field-of-view normalization to minimize mismatch in different subjects' images. It aids that streamline analysis of large-scale brain MRI datasets.

Proper citation: NeuroImage Field-of-View Normalization Tool (RRID:SCR_015957) Copy   

•   Source: SciCrunch Registry

https://github.com/ABCD-STUDY/FIONASITE

Software for uploading data to FIONA and capturing MR images and k-space data from medical image systems. It provides a web-interface to automate the data review (image viewer), integrate with the centralized electronic data record for assigning anonymized id's, and forward the data to the central archive.

Proper citation: FIONASITE (RRID:SCR_016012) Copy   

•   Source: SciCrunch Registry

https://github.com/ABCD-STUDY/Minimally-Processed-Image-Sharing

Software to share ABCD minimally processed data. It uploads minimally-processed MRI data to the NDA ( Non-Disclosure Agreement) ABCD (Adolescent Brain Cognitive Development) repository.

Proper citation: Minimally-Processed-Image-Sharing (RRID:SCR_016016) Copy   

•   Source: SciCrunch Registry

https://github.com/ABCD-STUDY/enroll

Software which provides a framework for the secure storage of Personal Identifyable Information (PII) for a multi-site longitudinal project centrally. Used in Adolescent Brain Cognitive Development (ABCD) Study.

Proper citation: enroll (RRID:SCR_016011) Copy   

•   Source: SciCrunch Registry

http://standage.github.io/AEGeAn

Software toolkit for the analysis and evaluation of genome annotations. The toolkit includes a variety of analysis programs, e.g. for comparing distinct sets of gene structure annotations (ParsEval), computation of gene loci (LocusPocus) and more.

Proper citation: Aegean (RRID:SCR_015965) Copy   

•   Source: SciCrunch Registry

http://www.aevol.fr/

Simulation software for experimental evolution of microorganisms. Aevol is a digital genetics model for the study of structural variations of the genome (e.g. number of genes, synteny, proportion of coding sequences).

Proper citation: Aevol (RRID:SCR_015966) Copy   

•   Source: SciCrunch Registry

https://github.com/EvolBioInf/andi

Software tool for rapidly computing and estimating evolutionary distance between closely related genomes. Because andi does not compute full alignments it scales even up to thousands of bacterial genomes.

Proper citation: andi (RRID:SCR_015971) Copy   

•   Source: SciCrunch Registry

https://github.com/ABCD-STUDY/tick-tock

Software for research study observation that visualizes study related events per day. Any event generating function sends a 'tick' event to this application which will be visible on this applications web-interface.

Proper citation: tick-tock (RRID:SCR_016023) Copy   

•   Source: SciCrunch Registry

https://bioinf.eva.mpg.de/anfo/

Software for short read alignment and mapping of sequencing reads where the DNA sequence is somehow modified and/or there is more divergence between sample and reference than what fast mappers will handle.

Proper citation: Anfo (RRID:SCR_015972) Copy   

•   Source: SciCrunch Registry

https://github.com/ABCD-STUDY/FIONA-protocol-compliance

Software that contains multiple sequential lines of MATLAB commands and function calls for numerical computing for ABCD study protocol compliance.

Proper citation: FIONA-protocol-compliance (RRID:SCR_016027) Copy   

•   Source: SciCrunch Registry

https://github.com/ABCD-STUDY/Fast-Track-Image-Sharing

Software for sharing the ABCD (Adolescent Brain Cognitive Development) study data on the National Data Archive (NDA).

Proper citation: Fast-Track-Image-Sharing (RRID:SCR_016021) Copy   

•   Source: SciCrunch Registry