Variant Analysis — Editorial Board Home

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Editorial Board

orcid logoBérénice Batut avatar Bérénice BatutAnton Nekrutenko avatar Anton Nekrutenkoorcid logoWolfgang Maier avatar Wolfgang Maierorcid logoBjörn Grüning avatar Björn Grüning

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Topic Materials

Material Contributions v2 help Pre-requisites help Follow up trainings Data on Zenodo Notebook Server Compatibility
Introduction to Variant analysis
Calling variants in diploid systems
Calling variants in non-diploid systems
Calling very rare variants
Microbial Variant Calling
Mapping and molecular identification of phenotype-causing mutations
Avian influenza viral strain analysis from gene segment sequencing data
From NCBI's Sequence Read Archive (SRA) to Galaxy: SARS-CoV-2 variant analysis
M. tuberculosis Variant Analysis
Mutation calling, viral genome reconstruction and lineage/clade assignment from SARS-CoV-2 sequencing data
Pox virus genome analysis from tiled-amplicon sequencing data
Exome sequencing data analysis for diagnosing a genetic disease
Identification of somatic and germline variants from tumor and normal sample pairs
Somatic Variant Discovery from WES Data Using Control-FREEC
Trio Analysis using Synthetic Datasets from RD-Connect GPAP
Querying the University of Bradford GDC Beacon Database for Copy Number Variants (CNVs)
Working with Beacon V2: A Comprehensive Guide to Creating, Uploading, and Searching for Variants with Beacons

Topic Workflows

Material Workflow Updated Version Tests Reports Comments
Calling variants in diploid systems Diploid Dec 21, 2024 3
Calling variants in non-diploid systems Calling variants in non-diploid systems Dec 21, 2024 2
Calling very rare variants Du Novo GTN Tutorial - Make Consensus Sequences Dec 21, 2024 3
Calling very rare variants Du Novo GTN Tutorial - Variant Calling Dec 21, 2024 3
Microbial Variant Calling Microbial Variant Calling Dec 21, 2024 4
Mapping and molecular identification of phenotype-causing mutations Mapping And Molecular Identification Of Phenotype Causing Mutations Dec 21, 2024 3
From NCBI's Sequence Read Archive (SRA) to Galaxy: SARS-CoV-2 variant analysis Simple COVID-19 - PE Variation Dec 21, 2024 1
M. tuberculosis Variant Analysis TB Variant Analysis v1.0 Dec 21, 2024 7
Pox virus genome analysis from tiled-amplicon sequencing data pox-virus-tiled-amplicon-ref-masking Dec 21, 2024 2
Exome sequencing data analysis for diagnosing a genetic disease Exome Seq Training Pre-Mapped W Cached Ref Dec 21, 2024 5
Exome sequencing data analysis for diagnosing a genetic disease Exome Seq Training Full W Cached Ref Dec 21, 2024 5
Identification of somatic and germline variants from tumor and normal sample pairs Identification of somatic and germline variants from tumor and normal sample pairs tutorial Dec 21, 2024 1
Somatic Variant Discovery from WES Data Using Control-FREEC Somatic-Variant-Discovery-from-WES-Data-Using-Control-FREEC Dec 21, 2024 1
Trio Analysis using Synthetic Datasets from RD-Connect GPAP Trio Analysis Tutorial Dec 21, 2024 5

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TODO once this is merged: https://github.com/galaxyproject/training-material/pull/4963

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