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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 87 showing 1721 ~ 1740 out of 2,279 results
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  • RRID:SCR_018551

    This resource has 1000+ mentions.

https://github.com/voutcn/megahit

Software tool as Next Generation Sequencing assembler. Optimized for metagenomes, but also works well on generic single genome assembly (small or mammalian size) and single cell assembly. Can assemble genome sequences from metagenomic datasets of hundreds of Giga base-pairs in time and memory efficient manner on single server.

Proper citation: MEGAHIT (RRID:SCR_018551) Copy   


  • RRID:SCR_018965

    This resource has 10+ mentions.

http://ccb.jhu.edu/software/stringtie/gff.shtml

Open source software tool to manipulate files in GFF format. Used to convert, sort, filter, transform, or cluster genomic features.

Proper citation: gffread (RRID:SCR_018965) Copy   


  • RRID:SCR_018966

    This resource has 10+ mentions.

https://github.com/nanoporetech/pychopper

Software tool to identify, orient and trim full length Nanopore cDNA reads. Able to rescue fused reads.

Proper citation: Pychopper (RRID:SCR_018966) Copy   


  • RRID:SCR_017633

    This resource has 10+ mentions.

https://github.com/BGI-Qingdao/TGS-GapCloser

Software tool that uses long reads to enhance genome assembly. Fast and accurate gap closing software tool that uses low coverage of error-prone long reads generated by third generation sequence techniques (Pacbio, Oxford Nanopore, etc.) or preassembled contigs for large genomes.

Proper citation: TGS-GapCloser (RRID:SCR_017633) Copy   


  • RRID:SCR_018929

    This resource has 10+ mentions.

https://github.com/brentp/mosdepth

Software command line tool for rapidly calculating genome wide sequencing coverage. Measures depth from BAM or CRAM files at either each nucleotide position in genome or for sets of genomic regions. Used for fast BAM/CRAM depth calculation for WGS, exome, or targeted sequencing quick coverage calculation for genomes and exomes.

Proper citation: mosdepth (RRID:SCR_018929) Copy   


  • RRID:SCR_017560

    This resource has 1+ mentions.

https://github.com/AnacletoLAB/parSMURF

Open source software package as high performance computing imbalance aware machine learning tool for genome wide detection of pathogenic variants.

Proper citation: parSMURF (RRID:SCR_017560) Copy   


  • RRID:SCR_018663

    This resource has 1+ mentions.

https://github.com/hms-dbmi/EHRtemporalVariability

Software R package for delineating temporal dataset shifts in electronic health records. Functions to delineate temporal dataset shifts in electronic health records through projection and visualization of dissimilarities among data temporal batches.Enables exploration and identification of dataset shifts, contributing to broadly examine and repurpose large, longitudinal datasets. Used to help ensure reliable data reuse to biomedical data users.

Proper citation: EHRtemporalVariability (RRID:SCR_018663) Copy   


  • RRID:SCR_019259

    This resource has 1+ mentions.

https://github.com/nch-igm/rna-stability

Software tool as parallel processing framework for large scale generation of secondary RNA structures and folding statistics for transcriptome of any species.

Proper citation: rna-stability (RRID:SCR_019259) Copy   


  • RRID:SCR_019233

    This resource has 1+ mentions.

https://radar-base.org/index.php/home/about-us/

Open source mobile health platform for collecting, monitoring, and analyzing data using sensors, wearables, and mobile devices. Enables study design and set up, active and passive remote data collection, secure data transmission via Wifi and/or Bluetooth and scalable solutions for data storage, management and access. Allows study participants to share their health data with clinicians and researchers in secure way.

Proper citation: RADAR-base (RRID:SCR_019233) Copy   


  • RRID:SCR_023996

https://github.com/Washington-University/CiftiLib

Software C++ Library for reading and writing CIFTI-2 and CIFTI-1 files.

Proper citation: CiftiLib (RRID:SCR_023996) Copy   


  • RRID:SCR_024065

    This resource has 1+ mentions.

https://github.com/rvaser/bioparser/

Software C++ library for parsing several formats in bioinformatics. C++ header only parsing library for several bioinformatics formats (FASTA/Q, MHAP/PAF/SAM), with support for zlib compressed files.

Proper citation: Bioparser (RRID:SCR_024065) Copy   


  • RRID:SCR_024062

    This resource has 1+ mentions.

https://github.com/biod/BioD

Software memory efficient bioinformatics library written in D programming language whose aim is to provide platform for developing high performance computational biology applications using the D programming language through automatic parallelization of tasks where possible and by avoiding unnecessary memory allocations.

Proper citation: BioD (RRID:SCR_024062) Copy   


  • RRID:SCR_023981

    This resource has 1+ mentions.

https://github.com/IRCAD-IHU/camp

Software multi-purpose reflection library developped by Technogerma Systems France and then by Tegesoft. Provides extra layer of flexibility to programs, and allows them to fully expose their data structures at runtime.

Proper citation: CAMP (RRID:SCR_023981) Copy   


  • RRID:SCR_024030

https://github.com/ggonnella/gfapy

Software library for handling sequence graphs in Python.

Proper citation: GfaPy (RRID:SCR_024030) Copy   


  • RRID:SCR_023976

http://www.bali-phy.org

Software application as simultaneous Bayesian inference of alignment and phylogeny. Used to estimate multiple sequence alignments and evolutionary trees from DNA, amino acid, or codon sequences. to explore the joint space of alignment and phylogeny given molecular sequence data. BAli-Phy version 3 is model based co-estimation of alignment and phylogeny. Version 3 is substantially faster for large trees, and implements covarion models, additional codon models and other new models. Implements ancestral state reconstruction, allows prior selection for all model parameters, and can also analyze multiple genes simultaneously.

Proper citation: BAli-Phy (RRID:SCR_023976) Copy   


  • RRID:SCR_024043

https://ismrmrd.github.io/apidocs/1.5.0/

Prerequisite for sharing magnetic resonance imaging reconstruction algorithms and code is a common raw data format. This repository describes such common raw data format, which attempts to capture the data fields that are required to describe the magnetic resonance experiment with enough detail to reconstruct images. The repository also contains a C/C++ library for working with the format.

Proper citation: ISMRMRD (RRID:SCR_024043) Copy   


  • RRID:SCR_023985

    This resource has 1+ mentions.

https://cdk.github.io/

Open Source software modular Java libraries for cheminformatics.

Proper citation: CDK (RRID:SCR_023985) Copy   


  • RRID:SCR_024039

https://github.com/gramos/imagetooth

Software library to generate images for odontograms.Allows to choose between png or jpg images.

Proper citation: ImageTooth (RRID:SCR_024039) Copy   


  • RRID:SCR_024090

https://github.com/rdpstaff/TaxonomyTree

Software library used by other RDP tools.TaxonomyTree building and traversal utility classes.

Proper citation: TaxonomyTree (RRID:SCR_024090) Copy   


  • RRID:SCR_024092

https://metacpan.org/dist/Sort-Key-Top

Functions available from this module select the top n elements from a list using several common orderings and custom key extraction procedures.

Proper citation: Sort-Key-Top (RRID:SCR_024092) Copy   



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