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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 99 showing 1961 ~ 1980 out of 2,279 results
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  • RRID:SCR_024335

    This resource has 10+ mentions.

https://odelaneau.github.io/shapeit4/

Software tool for estimation of haplotypes aka phasing for SNP array and high coverage sequencing data. The version 4 is refactored and improved version of SHAPEIT algorithm with multiple key additional features.

Proper citation: shapeit4 (RRID:SCR_024335) Copy   


  • RRID:SCR_023995

    This resource has 100+ mentions.

https://card.mcmaster.ca/

Comprehensive antibiotic resistance database. Bioinformatic database of resistance genes, their products and associated phenotypes.

Proper citation: CARD (RRID:SCR_023995) Copy   


  • RRID:SCR_024326

    This resource has 1+ mentions.

https://www.cs.cmu.edu/~ckingsf/software/sailfish/

Software tool that implements novel, alignment free algorithm for estimation of isoform abundances directly from set of reference sequences and RNA-seq reads.

Proper citation: sailfish (RRID:SCR_024326) Copy   


  • RRID:SCR_024206

    This resource has 1+ mentions.

https://github.com/fenderglass/Ragout/

Software tool for chromosome level scaffolding using multiple references. Given initial assembly fragments and one or multiple related references it produces chromosome scale assembly.

Proper citation: ragout (RRID:SCR_024206) Copy   


  • RRID:SCR_024066

    This resource has 1+ mentions.

https://metacpan.org/dist/Bio-SamTools

Software Perl interface to SamTools library for DNA sequencing.

Proper citation: Bio-SamTools (RRID:SCR_024066) Copy   


  • RRID:SCR_024341

    This resource has 1+ mentions.

https://github.com/ncbi/SKESA

Software de-novo sequence read assembler for microbial genomes.Designed to create breaks at repeat regions in the genome. This leads to excellent sequence quality without significantly compromising contiguity.SKESA contigs could be connected into GFA graph using GFA connector.

Proper citation: skesa (RRID:SCR_024341) Copy   


  • RRID:SCR_024342

    This resource has 10+ mentions.

https://github.com/phac-nml/sistr_cmd

SISTR command-line tool. Open web accessible tool for rapidly typing and subtyping draft salmonella genome assemblies.

Proper citation: sistr (RRID:SCR_024342) Copy   


  • RRID:SCR_024068

https://metacpan.org/dist/Bio-SCF

Software Perl extension for reading and writting SCF sequence files.This module provides Perl interface to SCF DNA sequencing files. It has both tied hash and an object-oriented interfaces. It provides the ability to read fields from SCF files and limited ability to modify them and write them back.

Proper citation: Bio-SCF (RRID:SCR_024068) Copy   


  • RRID:SCR_024184

https://github.com/COMBINE-lab/pufferfish

Software tool implementing novel indexing data structure for compacted de Bruijn graph and colored compacted de Bruijn graph.

Proper citation: pufferfish (RRID:SCR_024184) Copy   


  • RRID:SCR_024320

https://github.com/davidsoergel/rtax/

Software tool for rapid and accurate taxonomic classification of short paired-end sequence reads from the 16S ribosomal RNA gene.

Proper citation: rtax (RRID:SCR_024320) Copy   


  • RRID:SCR_024321

https://github.com/narunlifescience/runcircos-gui

GUI tool to run circos

Proper citation: runcircos-gui (RRID:SCR_024321) Copy   


  • RRID:SCR_024201

https://autodock.scripps.edu/resources/raccoon/

Software graphical interface for preparing AutoDock virtual screenings.Automates some of the most common operations performed when preparing virtual screening.

Proper citation: raccoon (RRID:SCR_024201) Copy   


  • RRID:SCR_023984

https://camitk.imag.fr/

Software Computer Assisted Medical Intervention Tool Kit helps researchers and clinicians to easily and rapidly collaborate in order to prototype CAMI applications, that feature medical images, surgical navigation and biomechanical simulations.Open source, cross-platform generic tool, written in C++, which can handle medical images, surgical navigations and biomechanical simulations.

Proper citation: CamiTK (RRID:SCR_023984) Copy   


  • RRID:SCR_024316

https://github.com/aberer/RogueNaRok

Software tool as versatile and scalable algorithm for rogue taxon identification. Also includes implementations of the maximum agreement subtree, leaf stability index and taxonomic instability index.

Proper citation: roguenarok (RRID:SCR_024316) Copy   


  • RRID:SCR_024318

http://faculty.washington.edu/tathornt/software/ROADTRIPS2/

Software C program that performs single SNP, case control association testing in samples with partially or completely unknown population and pedigree structure.

Proper citation: roadtrips (RRID:SCR_024318) Copy   


  • RRID:SCR_024372

https://github.com/brentp/vcfanno

Software tool for flexible annotation of genetic variants.Extracts and summarizes attributes from multiple annotation files and integrates annotations within INFO column of the original VCF file.

Proper citation: vcfanno (RRID:SCR_024372) Copy   


  • RRID:SCR_024091

    This resource has 1+ mentions.

https://github.com/walaj/SeqLib

Software C++ htslib/bwa-mem/fermi interface for interrogating sequence data

Proper citation: SeqLib (RRID:SCR_024091) Copy   


  • RRID:SCR_024371

    This resource has 100+ mentions.

https://bitbucket.org/genomicepidemiology/virulencefinder

Software tool for detection of E. coli virulence genes. Used to identify viruelnce genes in total or partial sequenced isolates of bacteria. E. coli, Enterococcus, S. aureus and Listeria are available.for detection of E. coli virulence genes.

Proper citation: VirulenceFinder (RRID:SCR_024371) Copy   


  • RRID:SCR_024351

http://www.bioinformatics.org/strap/

Software tool as Intuitive Editor for annotated multiple Sequence and Structure Alignments.

Proper citation: strap-base (RRID:SCR_024351) Copy   


  • RRID:SCR_024195

    This resource has 10+ mentions.

https://github.com/nanoporetech/qcat

Software Python command-line tool for demultiplexing Oxford Nanopore reads from FASTQ files.

Proper citation: qcat (RRID:SCR_024195) Copy   



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