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SciCrunch Registry is a curated repository of scientific resources, with a focus on biomedical resources, including tools, databases, and core facilities - visit SciCrunch to register your resource.

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On page 414 showing 8261 ~ 8280 out of 27,341 results
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https://www.ars-grin.gov/npgs/

Cooperative effort by U.S. state and federal government and private organizations to preserve the genetic diversity of plants. The NPGS aids scientists and the need for genetic diversity by acquiring, preserving, evaluating, documenting and distributing crop germplasm. The NPGS is managed by the Agricultural Research Service (ARS), the in-house research agency of the United States Department of Agriculture (USDA). Funding for the NPGS comes primarily through appropriations from the U.S. Congress.

Proper citation: National Plant Germplasm System (NPGS) (RRID:SCR_016785) Copy   


  • RRID:SCR_016305

    This resource has 1+ mentions.

http://www.vilber.de/en/products/analysis-software/capt-software/

Software for molecular weight, quantification of bands, colony counting and distance calculation in Vilber Lourmat gel documentation imaging systems. Used in molecular biology laboratories.

Proper citation: CAPT (RRID:SCR_016305) Copy   


http://www.bioinformatics.org/xacg/wiki/

Molecular computing based on XNA-built alphabets.

Proper citation: Xenonucleic Acid Computing Group Wiki Template (RRID:SCR_016905) Copy   


  • RRID:SCR_016597

https://www.niaid.nih.gov/about/cyber-infrastructure-computational-biology-contacts

Office of Cyber Infrastructure and Computational Biology of NIAID.

Proper citation: OCICB (RRID:SCR_016597) Copy   


  • RRID:SCR_016991

    This resource has 10+ mentions.

http://www.biosoft.com/w/assayzap.htm

Software tool as universal assay calculator for RIA, ELISA, IRMA, colorimetric or any other type of assay by Biosoft. Maintains record for each assay, and enables standard curve and QCs to be compared and adjusted. Can process data from 96 and 384-well plate readers in any order.

Proper citation: AssayZap (RRID:SCR_016991) Copy   


  • RRID:SCR_015666

    This resource has 1+ mentions.

http://doa.nubic.northwestern.edu/pages/search.php

Project portal for a collaborative database aiming to provide a comprehensive annotation to human genome.It uses the computable, controlled vocabulary of Disease Ontology (DO) and NCBI Gene Reference Into Function (GeneRIF).

Proper citation: DOAF (RRID:SCR_015666) Copy   


https://www.ncbi.nlm.nih.gov/UniGene/help.cgi?item=DDD

Software tool for comparing EST profiles in order to identify genes with significantly different expression levels.

Proper citation: Digital Differential Display (DDD) (RRID:SCR_016638) Copy   


  • RRID:SCR_015707

    This resource has 1+ mentions.

https://github.com/eead-csic-compbio/split_pairs

Software for processing NGS sequence reads in FASTQ and FASTA formats. split_pairs.pl is suited particularly for the task of sorting pair end reads and for modifying their headers with Perl-style regular expressions.

Proper citation: split_pairs.pl (RRID:SCR_015707) Copy   


  • RRID:SCR_015790

    This resource has 10+ mentions.

http://www.gelifesciences.co.kr/wp-content/uploads/2016/08/IN-Cell-Developer-Toolbox-v1.9.pdf

Image analysis software for developing new cellular assay analysis routines. This software provides a selection of advanced segmentation, pre-processing and post-postprocessing tools.

Proper citation: INCell Developer Toolbox (RRID:SCR_015790) Copy   


https://www.ruhr-uni-bochum.de/mpc/software/ProCon/index.html.en

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.

Proper citation: ProCon - PROteomics CONversion (RRID:SCR_016363) Copy   


  • RRID:SCR_016966

    This resource has 100+ mentions.

https://github.com/wdecoster/nanofilt

Software tool written in Python to perform its filtering based on mean read quality and GC content and read length. Used for filtering and trimming of long read sequencing data.

Proper citation: NanoFilt (RRID:SCR_016966) Copy   


http://monogenicdiabetes.uchicago.edu/mody-registry-2/

Research project that aims to learn more about the number of people who have monogenic diabetes, why and how it happens, and how best to treat it. Any adult or child with a known genetic cause of diabetes may join the MODY Registry.

Proper citation: Monogenic Diabetes Registry (RRID:SCR_015883) Copy   


  • RRID:SCR_017025

    This resource has 1+ mentions.

https://github.com/mandricigor/ScaffMatch

Software tool as scaffolding algorithm based on maximum weight matching able to produce high quality scaffolds from next generation sequencing data (reads and contigs). Able to handle reads with both short and long insert sizes.

Proper citation: ScaffMatch (RRID:SCR_017025) Copy   


  • RRID:SCR_016331

    This resource has 100+ mentions.

https://www.brainproducts.com/productdetails.php?id=21

Software for multifunctional recording designed to provide Brain Products GmbH- Solutions for Neurophysiological Research amplifier with a platform for recording setup and execution.

Proper citation: BrainVision Recorder (RRID:SCR_016331) Copy   


  • RRID:SCR_017024

    This resource has 1+ mentions.

https://www.adinstruments.com/products/dmt-normalization

Software tool for calculating optimal pretension conditions for microvascular or any small tubular tissue research. DMT Normalization Add-On, provided by ADInstruments, is included as part of LabChart Pro or can be purchased separately.

Proper citation: DMT Normalization (RRID:SCR_017024) Copy   


http://www.ngsp.org

Project that aims to standardize Hemoglobin A1c test results to those of the Diabetes Control and Complications Trial (DCCT) and United Kingdom Prospective Diabetes Study (UKPDS) which established the direct relationships between HbA1c levels and outcome risks in patients with diabetes.

Proper citation: National Glycohemoglobin Standardization Program (RRID:SCR_015885) Copy   


  • RRID:SCR_017303

    This resource has 1+ mentions.

https://bitbucket.org/nicofmay/basta-bayesian-structured-coalescent-approximation/src/master/

Software package as Bayesian method to infer migration from genetic data. Implemented in BEAST2 that combines accuracy of methods based on structured coalescent with computational efficiency required to handle more than few populations.

Proper citation: BASTA (RRID:SCR_017303) Copy   


  • RRID:SCR_016978

    This resource has 1+ mentions.

https://geomagic-studio.software.informer.com/12.0/

Software tool to convert 3D scans into parametric models. Transforms 3D scan data into highly accurate surface, polygon and native CAD models. Used for reverse engineering, product design, rapid prototyping and analysis.

Proper citation: GEOMAGIC Studio (RRID:SCR_016978) Copy   


  • RRID:SCR_015897

    This resource has 100+ mentions.

https://github.com/dvera/albacore

Data processing basecaller for the Oxford Nanopore sequencer that identifies DNA sequences directly from raw data. It enhances accuracy of the single-read sequence data, contributing to high consensus accuracy for nanopore sequence data.

Proper citation: Albacore (RRID:SCR_015897) Copy   


https://www.nsrusa.org

Organization that provides instructions for and research on the Natural Stress Relief (NSR) meditation method.

Proper citation: Natural Stress Relief (RRID:SCR_015898) Copy   



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