Curator Dashboard

Software tool for imputation of viral whole genome sequences from partially sequenced samples. Software tool for imputation of whole-genome SARS-CoV-2 sequences.

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• SciCrunch
• 5 years ago - submitted by Francisco M. Ortuño Guzmán

Institute is entirely devoted to psycholinguistics – the study of how we produce and understand language, and how we acquire these skills as first or second language learners. The only institution in the world entirely dedicated to psycholinguistics, and is also one of only three among total of 90 within the Max Planck Society to be located outside Germany.

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• RRID-Legacy
• 5 years ago - submitted by Edyta Vieth

Software annotation tool for audio and video recordings. Annotation can be sentence, word or gloss, comment, translation or description of any feature observed in media. Annotations can be created on multiple layers. Tiers can be hierarchically interconnected. Annotation can either be time-aligned to media or it can refer to other existing annotations. Content of annotations consists of Unicode text and annotation documents are stored in XML format (EAF).

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• RRID-Legacy
• 5 years ago - by Anonymous

Data portal as part of Human BioMolecular Atlas Program. Data available on HuBMAP Portal is open access data to be used for research of human biology. Certain data types with potential for re-identification are available in restricted access either directly through this portal by login-dependent permissions or through dbGAP. All data users are expected to respect privacy and confidentiality of donors who provided samples. Data are not to be used to re-identify donors or their family members without further approval from HuBMAP. Data for single-cell, three-dimensional maps of various human tissues. Data include discrete, complex organs (kidney, ureter, bladder, lung, breast, small intestine and colon); distributed organ systems (vasculature); systems comprising dynamic or motile cell types with distinct microenvironments (lymphatic organs: spleen, thymus, and lymph nodes).

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• dkNET
• 5 years ago - submitted by Ko-Wei Lin

Platform for supporting systematic drug–target identification and prioritisation.Provides users with queryable knowledgebase and user interface to aid systematic target identification and prioritisation for drug discovery based upon underlying evidence.

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• dkNET
• 5 years ago - submitted by Ko-Wei Lin

Portal offers features to help discover associations between genes, variants, and traits including Browse and rank gene and variant associations identified by Locus-to-Gene (L2G) scoring pipeline, Uncover credible sets for variant and trait associations based on mapping analyses pipeline, Explore and compare studies from UK Biobank, FinnGen, and GWAS Catalog using multi-trait comparison tool eQTL Catalogue.

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• dkNET
• 5 years ago - submitted by Ko-Wei Lin

Catalog provides uniformly processed gene expression and splicing QTLs from all available public studies on human. Expression and splicing QTLs recomputed from public datasets.

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• dkNET
• 5 years ago - submitted by Ko-Wei Lin

Software pacakge that uses Levenshtein Distance to calculate differences between sequences for string matching.

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• RRID-Legacy
• 5 years ago - by Anonymous

Software Python package to tackle curse of imbalanced datasets in machine learning.Offers number of re-sampling techniques commonly used in datasets showing strong between class imbalance.

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• RRID-Legacy
• 5 years ago - by Anonymous

Software tool as gradient boosting framework that uses tree based learning algorithms. Designed to be distributed and efficient with advantages:Faster training speed and higher efficiency;Lower memory usage;Better accuracy;Support of parallel, distributed, and GPU learning;Capable of handling large scale data.

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• RRID-Legacy
• 5 years ago - by Anonymous

Software tool as wrapper feature selection method which combines both Boruta feature selection algorithm with shapley values.

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• RRID-Legacy
• 5 years ago - by Anonymous

Open source, low code machine learning library in Python that allows you to go from preparing your data to deploying your model within minutes in your choice of notebook environment.

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• RRID-Legacy
• 5 years ago - by Anonymous

Software package for gradient boosting on decision trees library. Used for ranking, classification, regression and other ML tasks.

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• RRID-Legacy
• 5 years ago - by Anonymous

System used for detection of chemiluminescence, fluorescence, colorimetry,densitometry, gel documentation. It has been replaced by ChemiDoc Imager. BioRad continues to provide support for customers with ChemiDoc Touch Systems.

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• RRID-Legacy
• 5 years ago - by Anonymous

Software pipeline to process and analyse RNAseq data. Contains files needed to process and analyse RNAseq data.

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• RRID-Legacy
• 5 years ago - submitted by Mario de Bono

Software tool for PRAGUI pipeline exploratory analysis.

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• RRID-Legacy
• 5 years ago - submitted by Mario de Bono

Portal created to help openly explore and share NF datasets, analysis tools, resources, and publications related to neurofibromatosis and schwannomatosis.Public data repository that stores and shares data generated by multiple collaborative research programs focused on neurofibromatosis diseases.

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• RRID-Legacy
• 5 years ago - submitted by Robert Allaway

Software suite of interoperable software tools designed for global community of public health practitioners and researchers. Provides easy data entry form and database construction, customized data entry experience, and data analysis with epidemiologic statistics, maps, and graphs for public health professionals who may lack information technology background.Statistical software for epidemiology developed by Centers for Disease Control and Prevention in Atlanta, Georgia. Available for Microsoft Windows, Android and iOS, along with web and cloud version.

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• RRID-Legacy
• 5 years ago - by Anonymous

Nonprofit organization with mission to work with companies and governments to build open, trustworthy data ecosystem. They work with range of organisations, governments, public bodies and civil society to create world where data works for everyone.

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• RRID-Legacy
• 5 years ago - by Anonymous

Software tool as fast principal component analysis of large scale genome wide data. FlashPCA performs fast principal component analysis (PCA) of single nucleotide polymorphism (SNP) data. FlashPCA2 used for principal component analysis of biobank scale genotype datasets.

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• RRID-Legacy
• 5 years ago - by Anonymous