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Showing 20 out of 28,805 Resources on page 318

PanglaoDB

Database for exploration of single cell RNA sequencing experiments from mouse and human. Collects and integrate data from multiple studies and present them through unified framework.

  • Resource
  • RRID
  • 4 years ago - by Anonymous

richR

Software package to provide functions richGO, richKEGG,and enrich to do functional enrichment analysis. Used for function enrichment analysis and network construction.

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  • RRID
  • 4 years ago - by Anonymous

Coselens

Software R package to detect gene level differential selection between two groups of samples.Used for calculation of excess of non synonymous mutations between two groups.

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  • ADC
  • 4 years ago - by Anonymous

ConnecTF

Software platform to integrate transcription factor gene interactions and validate regulatory networks. Gene regulatory network validation.

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  • RRID
  • 4 years ago - by Anonymous

VirtualPlant

Software platform to support systems biology research. Integrates genomic data and provides visualization and analysis tools for exploration of genomic data. Provides tools to generate biological hypotheses.

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  • RRID
  • 4 years ago - by Anonymous

ggforce

Software R package providing missing functionality to ggplot2 through extension system introduced with ggplot2 v2.0.0.

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  • RRID
  • 4 years ago - by Anonymous

janitor

Software R package to format data, frame column names, provide quick counts of variable combinations and isolate duplicate records, format tabulation results.

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  • RRID
  • 4 years ago - by Anonymous

Deep cryo-EM Map Enhancer

Software Python package to perform post-processing of cryo-EM maps. Deep learning model trained on pairs of experimental volumes and atomic model corrected volumes that is able to obtain post-processed maps using as input raw volumes, preferably half maps.

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  • RRID
  • 4 years ago - by Anonymous

learnMSA

Software tool as multiple sequence alignment formulated as statistical machine learning problem, where optimal profile hidden Markov model for potentially very large family of protein sequences is searched and alignment is decoded.

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  • RRID
  • 4 years ago - by Anonymous

sei

Web server for systematically predicting sequence regulatory activities and applying sequence information to human genetics data. Provides global map from any sequence to regulatory activities, as represented by sequence classes, and each sequence class integrates predictions for chromatin profiles like transcription factor, histone marks, and chromatin accessibility profiles across wide range of cell types.

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

pMAT

Open source software suite for analysis of fiber photometry data.

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  • RRID
  • 4 years ago - submitted by Jensen Palmer

NCBI Datasets

Platform to let you gather data from across NCBI databases. Allows to find and download gene, transcript, protein and genome sequences, annotation and metadata.

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

Olympus: BX53 Upright Microscope

LED illuminator for BX53 is equivalent to or better than 100 W halogen lamp, delivering brightness appropriate for teaching or contrast methods. Can be customized for different observation methods, such as phase contrast and fluorescence, with modular components.

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  • RRID
  • 4 years ago - submitted by yaoxing dou

zmax_edf_merge_converter

Software tool for comprehensive conversion of folder with Hypnodyne zmax EDF files into merged European Data Format.

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  • RRID
  • 4 years ago - submitted by Frederik D. Weber

LINCS Data Portal 2.0

Primary access point for compendium of LINCS data with substantial changes in data architecture and APIs, completely redesigned user interface, and enhanced curated metadata annotations to support more advanced, intuitive and deeper querying, exploration and analysis capabilities. LINCS datasets are accessible at data point level enabling users to directly access and download any subset of signatures across entire library independent from originating source, project or assay. Newly designed query interface enables global metadata search with autosuggest across all annotations associated with perturbations, model systems, and signatures.

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  • RRID
  • 4 years ago - submitted by Caty Chung

Penn State College of Medicine Metabolic Phenotyping Core Facility

Supports research that requires comprehensive assessment of energy balance and body composition in experimental rodents by providing necessary equipment and expertise. Services include training in the use of equipment, consultation on experiment design, and help with data analysis. Instrumentation includes Bruker TD-NMR LF100 Minispec and TSE Phenomaster System with Integrated Stellar Telemetry.

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  • RRID
  • 4 years ago - submitted by Scot Kimball

SwissDock

Web service to predict molecular interactions that may occur between target protein and small molecule. Protein small molecule docking web service based on EADock DSS.

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  • SciCrunch
  • 4 years ago - by Anonymous

Intego

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.

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  • RRID
  • 4 years ago - by Anonymous

OrthoANIu

Software tool for calculating average nucleotide identity.

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  • RRID
  • 4 years ago - by Anonymous

BiG-SCAPE

Software tool that calculates distances between BGCs in order to map BGC diversity onto sequence similarity networks, which are then processed for automated reconstruction of Gene Cluster Families, groups of gene clusters that encode biosynthesis of highly similar or identical molecules.

  • Resource
  • RRID
  • 4 years ago - by Anonymous