Curator Dashboard

MiSeq FGx Forensic Genomics System is the first fully validated, next-generation sequencing (NGS) solution designed for forensic science. Dedicated library kits and analytical software take you from DNA-to-answer with streamlined efficiency.

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• SciCrunch
• 8 years ago - submitted by Isabella Froman

The NextSeq 550 System brings the power of a high-throughput sequencing system to your benchtop. With tunable output and high data quality, it provides the flexible power you need for whole-genome, transcriptome, and targeted resequencing.

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• SciCrunch
• 8 years ago - submitted by Isabella Froman

MiSeqDx System is FDA-regulated, CE-IVD-marked, NGS platform for in vitro diagnostic (IVD) testing. System offers both diagnostic and research modes.

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• SciCrunch
• 8 years ago - submitted by Isabella Froman

MiSeq System offers wide range of sequencing applications. Capable of automated paired end reads and up to 15 Gb per run, delivering over 600 bases of sequence data per read. The library prep kits are optimized for variety of applications, including targeted gene, small genome, and amplicon sequencing, 16S metagenomics.

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• SciCrunch
• 8 years ago - submitted by Isabella Froman

MiniSeq System to perform range of targeted DNA and RNA applications for low numbers of samples.

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• SciCrunch
• 8 years ago - submitted by Isabella Froman

Benchtop next-generation sequencer to sequence DNA and RNA.

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• SciCrunch
• 8 years ago - submitted by Anh Pham

Software for genomics and bioinformatics analysis. GenPipes includes several python pipelines that cover many genomics applications, such as RNASeq, ChIPSeq, DNASeq, WGBS, HiC, Metagenomics, PacBio assembly, etc.

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• SciCrunch
• 8 years ago - submitted by Rola Dali

Software that performs data analysis algorithms for QPCR data. The software is included with the purchase of the Agilent MxPro QPCR System., THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025.

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• RRID-Legacy
• 8 years ago - submitted by Timothy Errington

Software that detects kinase-specific phosphorylation sites. GPS provides a platform able to perform its prediction based on a group-based phosphorylation scoring algorithm. It allows users to query multiple protein sequences through a batch prediction mode.

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• RRID-Legacy
• 8 years ago - by Anonymous

Supplier of Frogs and Tadpoles for the scientific community.

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• SciCrunch
• 8 years ago - submitted by Philip Leo Pascual

Software toolkit for semantic integration of multi-modal brain data. It is used to collect, structure, connect, analyze and re-use brain data.

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• RRID-Legacy
• 8 years ago - by Anonymous

Software plugin for Fiji/ImageJ that performs retrospective image correction for optical microscopy. It is based on low rank and sparse decomposition, which corrects both shading in space and background bleaching in time.

• RRID-Legacy
• 8 years ago - submitted by Jia-Ren Lin

Center that is part of the NIH Library of Integrated Network-based Cellular Signatures (LINCS) Program. Its goals are to collect and disseminate data and analytical tools needed to understand how human cells respond to perturbation by drugs, the environment, and mutation.

• RRID-Legacy
• 8 years ago - submitted by Jia-Ren Lin

Database of death record information on file in state vital statistics offices. Working with these state offices, the National Center for Health Statistics (NCHS) established the NDI as a resource to aid epidemiologists and other health and medical investigators with their mortality ascertainment activities.

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• SciCrunch
• 8 years ago - submitted by Isabella Froman

Ultrafast and memory efficient tool for aligning sequencing reads to long reference sequences. Supports gapped, local, and paired end alignment modes. More suited to finding longer, gapped alignments in comparison with original Bowtie method.

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• RRID-Legacy
• 8 years ago - by Anonymous

Instrument that electronically monitors cells grown in tissue culture. It is a real-time, label-free, impedance-based method to study the activities of cells. Used for analysis in cell biological dynamics for cells that do not form tight monolayers such as cancer cell lines. The system supports communication to a PC, allowing data acquisition, analysis, and storage.

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• RRID-Legacy
• 8 years ago - by Anonymous

Python based tools to process, visualize and analyse high-throughput sequencing data, such as ChIP-seq, RNA-seq or MNase-seq. Implemented within Galaxy framework. Used to perform complete bioinformatic workflows ranging from quality controls and normalizations of aligned reads to integrative analyses, including clustering and visualization approaches.

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• RRID-Legacy
• 8 years ago - by Anonymous

Software application to perform systematic and collaborative curation of neuroscientific literature. Graphical User Interface (GUI) for the Python package NeuroAnnotation Toolbox (NAT). Used for the systematic annotation of relevant statements and model parameters to be traceable, reusable across projects, structured with controlled vocabularies.

• SciCrunch
• 8 years ago - submitted by Anita Bandrowski

Java based conversion tool for conversion of data from Proteomics files or a LIMS (Laboratory Information Management System) database into standard formats. Used to support wet-lab scientists in creating proteomics data files ready for upload into the public repositories.

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• SciCrunch
• 8 years ago - by Anonymous

Software as a scalable open-source service for platform-independent interactive visual analysis of biomedical data. It is a service and a library that work in tandem to equip existing platforms with visual analytical capabilities for explorative data analysis.

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• SciCrunch
• 8 years ago - submitted by Sascha Herzinger