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Update tool/resource_list.yaml (#378)
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Co-authored-by: bedroesb <[email protected]>
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github-actions[bot] and bedroesb authored Dec 16, 2024
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Showing 1 changed file with 11 additions and 3 deletions.
14 changes: 11 additions & 3 deletions _data/tool_and_resource_list.yml
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registry:
biotools: gtex
fairsharing: 293c15
tess: GTEx
url: https://gtexportal.org/
- description: HISAT2 is a fast and sensitive alignment program for mapping next-generation sequencing reads (whole-genome, transcriptome, and exome sequencing data) to a population of human genomes (as well as to a single reference genome).
id: hisat2
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name: MAFFT
registry:
biotools: MAFFT
tess: MAFFT
url: https://github.com/GSLBiotech/mafft
- description: Manta calls structural variants (SVs) and indels from mapped paired-end sequencing reads.
id: manta
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name: The Cancer Genome Atlas (TCGA)
registry:
fairsharing: m8wewa
tess: TCGA
tess: The Cancer Genome Atlas (TCGA)
url: https://www.cancer.gov/about-nci/organization/ccg/research/structural-genomics/tcga
- description: The Data Use Ontology (DUO) describes data use requirements and limitations. DUO allows to semantically tag datasets with restriction about their usage, making them discoverable automatically based on the authorization level of users, or intended usage. This resource is based on the OBO Foundry principles, and developed using the W3C Web Ontology Language. It is used in production by the European Genome-phenome Archive (EGA) at EMBL-EBI and CRG as well as the Broad Institute for the Data Use Oversight System (DUOS).
id: the-data-use-ontology
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registry:
biotools: ucsc_genome_browser
fairsharing: s22qdj
tess: UCSC Genome Browser
url: https://genome.ucsc.edu/
- description: Variant calling and somatic mutation/CNV detection for next-generation sequencing data
id: varscan
name: VarScan
registry:
biotools: varscan
tess: VarScan
url: https://github.com/dkoboldt/varscan
- description: VEP (Variant Effect Predictor) predicts the functional effects of genomic variants.
id: vep
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name: Bcftools
registry:
biotools: bcftools
tess: Bcftools
url: https://samtools.github.io/bcftools/bcftools.html
- description: Qualimap is a quality control tool that assesses the quality of the sequencing data at different stages of the analysis pipeline, including read mapping, coverage, and expression analysis.
id: qualimap
name: Qualimap
registry:
biotools: qualimap
tess: Qualimap
url: http://qualimap.conesalab.org/
- description: GATK is a widely used tool for variant calling and genotyping from NGS data.
id: gatk
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registry:
biotools: ols
fairsharing: Mkl9RR
tess: Ontology Lookup Service
tess: Ontology Lookup Service (OLS)
url: https://www.ebi.ac.uk/ols/index
- description: A comprehensive repository of biomedical ontologies
id: bioportal
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name: RAxML
registry:
biotools: raxml
tess: RAxML
url: https://github.com/stamatak/standard-RAxML
- description: IQ-TREE is designed to efficiently handle large phylogenomic datasets, utilize multicore and distributed parallel computing for faster analysis, and automatically resume interrupted analyses through checkpointing.
id: iqtree
name: IQtree
registry:
biotools: iqtree
tess: IQtree
url: https://github.com/iqtree/iqtree2
- description: MrBayes is a program for Bayesian inference and model choice across a wide range of phylogenetic and evolutionary models. MrBayes uses Markov chain Monte Carlo (MCMC) methods to estimate the posterior distribution of model parameters.
id: mrbayes
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name: SNippy
registry:
biotools: snippy
tess: SNippy
url: https://github.com/tseemann/snippy
- description: Convert ThermoFinningan RAW mass spectrometry files to the mzXML format.
id: readw
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name: MEGAHIT
registry:
biotools: megahit
tess: MEGAHIT
url: https://github.com/voutcn/megahit
- description: A taxonomic classification system using exact k-mer matches to achieve high accuracy and fast classification speeds.
id: kraken2
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