Rare Disease Pathway and Network Analysis
The European Joint Project on Rare Diseases (EJP-RD) and the Helis Academy organized a workshop with training for pathway and network analysis.
Keywords: Pathway analysis, Biological networks, Network analysis, Pathways
Resource type: Tutorial
Rare Disease Pathway and Network Analysis
https://laurendupuis.github.io/EJP-RD_Helis_Academy/
https://tess.elixir-europe.org/materials/rare-disease-pathway-and-network-analysis
The European Joint Project on Rare Diseases (EJP-RD) and the Helis Academy organized a workshop with training for pathway and network analysis.
Lauren Dupuis
Martina Kutmon
Friederike Ehrhart
Denise Slenter
Pathway analysis, Biological networks, Network analysis, Pathways
Life Science Researchers
Single cell RNA-seq data analysis using Chipster
This course introduces single cell RNA-seq data analysis. It covers the processing of transcript counts from quality control and filtering to dimensional reduction, clustering, and differential expression analysis. You will also learn how to do integrated analysis of two samples. We use Seurat v3...
Keywords: scRNA-seq
Resource type: Slides, Training materials
Single cell RNA-seq data analysis using Chipster
https://www.csc.fi/web/training/-/single-cell-chipster-2019
https://tess.elixir-europe.org/materials/single-cell-rna-seq-data-analysis-using-chipster
This course introduces single cell RNA-seq data analysis. It covers the processing of transcript counts from quality control and filtering to dimensional reduction, clustering, and differential expression analysis. You will also learn how to do integrated analysis of two samples. We use Seurat v3 tools embedded in the user-friendly Chipster software.
Eija Korpelainen
Maria Lehtivaara
scRNA-seq
Biologists
bioinformaticians
How to use the statistics module of ArrayAnalysis.org for statistics analysis of microarray data
This tutorial how to statistically analyze microarray data with ArrayAnalysis.org website.
Keywords: ArrayAnalysis.org, microarray
How to use the statistics module of ArrayAnalysis.org for statistics analysis of microarray data
https://enanomapper.github.io/tutorials/Statistics/readme.html
https://tess.elixir-europe.org/materials/how-to-use-the-statistics-module-of-arrayanalysis-org-for-statistics-analysis-of-microarray-data
This tutorial how to statistically analyze microarray data with ArrayAnalysis.org website.
Anwesha Bohler
Egon Willighagen
Friederike Ehrhart
Lars Eijssen
Linda Rieswijk
Penny Nymark
ArrayAnalysis.org, microarray
post-docs
Analysis of RNA-Seq using the DESeq2 package
Bioconductor provides tools for the analysis and comprehension of high-throughput genomic data.
Bioconductor uses the R statistical programming language, and is open source and open development.
It has two releases each year, 1560 software packages, and an...
Scientific topics: RNA-Seq
Analysis of RNA-Seq using the DESeq2 package
https://bioconductor.org2014/BioC2014/RNA-Seq-Analysis-Lab.pdf
https://tess.elixir-europe.org/materials/analysis-of-rna-seq-using-the-deseq2-package
Bioconductor provides tools for the analysis and comprehension of high-throughput genomic data.
Bioconductor uses the R statistical programming language, and is open source and open development.
It has two releases each year, 1560 software packages, and an active user community.
Bioconductor is also available as an AMI (Amazon Machine Image) and a series of Docker images.
Michael Love
RNA-Seq
Lecture: RNA-Seq data analysis and differential expression part II
Bioconductor provides tools for the analysis and comprehension of high-throughput genomic data.
Bioconductor uses the R statistical programming language, and is open source and open development.
It has two releases each year, 1560 software packages, and an...
Scientific topics: RNA-Seq
Lecture: RNA-Seq data analysis and differential expression part II
https://bioconductor.org2015/CSAMA2015/lect/L06-rna-stats-love.pdf
https://tess.elixir-europe.org/materials/lecture-rna-seq-data-analysis-and-differential-expression-part-ii
Bioconductor provides tools for the analysis and comprehension of high-throughput genomic data.
Bioconductor uses the R statistical programming language, and is open source and open development.
It has two releases each year, 1560 software packages, and an active user community.
Bioconductor is also available as an AMI (Amazon Machine Image) and a series of Docker images.
Michael Love
RNA-Seq
Low-level exploratory data analysis and methods development for RNA-seq
Bioconductor provides tools for the analysis and comprehension of high-throughput genomic data.
Bioconductor uses the R statistical programming language, and is open source and open development.
It has two releases each year, 1560 software packages, and an...
Scientific topics: RNA-Seq
Low-level exploratory data analysis and methods development for RNA-seq
https://bioconductor.org2016/BioC2016/ConcurrentWorkshops3/Love/bioc2016eda.html
https://tess.elixir-europe.org/materials/low-level-exploratory-data-analysis-and-methods-development-for-rna-seq
Bioconductor provides tools for the analysis and comprehension of high-throughput genomic data.
Bioconductor uses the R statistical programming language, and is open source and open development.
It has two releases each year, 1560 software packages, and an active user community.
Bioconductor is also available as an AMI (Amazon Machine Image) and a series of Docker images.
Michael Love
RNA-Seq
Gene-sets and correlation
Bioconductor provides tools for the analysis and comprehension of high-throughput genomic data.
Bioconductor uses the R statistical programming language, and is open source and open development.
It has two releases each year, 1560 software packages, and an...
Operations: Gene-set enrichment analysis
Gene-sets and correlation
https://bioconductor.org2016/CSAMA/lect-17-gene-set-enrichment/gene_set_correlations.pdf
https://tess.elixir-europe.org/materials/gene-sets-and-correlation
Bioconductor provides tools for the analysis and comprehension of high-throughput genomic data.
Bioconductor uses the R statistical programming language, and is open source and open development.
It has two releases each year, 1560 software packages, and an active user community.
Bioconductor is also available as an AMI (Amazon Machine Image) and a series of Docker images.
Michael Love
Robust statistics
Bioconductor provides tools for the analysis and comprehension of high-throughput genomic data.
Bioconductor uses the R statistical programming language, and is open source and open development.
It has two releases each year, 1560 software packages, and an...
Scientific topics: Statistics and probability
Robust statistics
https://bioconductor.org2016/CSAMA/lect-11-robust/robust.pdf
https://tess.elixir-europe.org/materials/robust-statistics
Bioconductor provides tools for the analysis and comprehension of high-throughput genomic data.
Bioconductor uses the R statistical programming language, and is open source and open development.
It has two releases each year, 1560 software packages, and an active user community.
Bioconductor is also available as an AMI (Amazon Machine Image) and a series of Docker images.
Michael Love
Statistics and probability
RNA-seq data analysis and differential expression
Bioconductor provides tools for the analysis and comprehension of high-throughput genomic data.
Bioconductor uses the R statistical programming language, and is open source and open development.
It has two releases each year, 1560 software packages, and an...
RNA-seq data analysis and differential expression
https://bioconductor.org2016/CSAMA/lect-06-rnaseq-analysis/rnaseq.pdf
https://tess.elixir-europe.org/materials/rna-seq-data-analysis-and-differential-expression
Bioconductor provides tools for the analysis and comprehension of high-throughput genomic data.
Bioconductor uses the R statistical programming language, and is open source and open development.
It has two releases each year, 1560 software packages, and an active user community.
Bioconductor is also available as an AMI (Amazon Machine Image) and a series of Docker images.
Michael Love
RNAseq
ELIXIR eLearning definitions
Materials from the asynchronous learning course "ELIXIR eLearning definitions"
Keywords: eLearning, training, EeLP
Resource type: course materials, Training materials, Documentation
ELIXIR eLearning definitions
https://elixir.mf.uni-lj.si/course/view.php?id=10
https://tess.elixir-europe.org/materials/elixir-elearning-definitions
Materials from the asynchronous learning course "ELIXIR eLearning definitions"
Brane Leskosek
Jure Dimec
Eija Korpelainen
Teresa Attwood
Sarah Morgan
Nicola Mulder
Celia van Gelder
Patricia Palagi
Brane Leskosek
Jure Dimec
Eija Korpelainen
Teresa Attwood
Sarah Morgan
Nicola Mulder
Celia van Gelder
Patricia Palagi
eLearning, training, EeLP
Researchers
teachers
Trainers
RNA-seq data analysis using Chipster
Materials from the ELIXIR tutorial “RNA-seq data analysis using Chipster”, Jan 31, 2017
Scientific topics: Transcriptomics, Genomics
Keywords: transcriptomics, RNA-Seq, eLearning, EeLP
Resource type: course materials, Training materials, Slides, Video
RNA-seq data analysis using Chipster
https://elixir.mf.uni-lj.si/course/view.php?id=9
https://tess.elixir-europe.org/materials/rna-seq-data-analysis-using-chipster
Materials from the ELIXIR tutorial “RNA-seq data analysis using Chipster”, Jan 31, 2017
Eija Korpelainen
Maria Lehtivaara
Eija Korpelainen
Maria Lehtivaara
Transcriptomics
Genomics
transcriptomics, RNA-Seq, eLearning, EeLP
Researchers
ELIXIR EXCELERATE Train the Trainer
This set of course material was designed in the context of the ELIXIR EXCELERATE Train the Trainer programme. It covers four sessions:
* Learning principles and how they apply to training and teaching
* Teaching techniques that can be used to enhance learner engagement and participation
*...
Keywords: Train the trainer, Pedagogy, Course development, Course design
Resource type: Training materials
ELIXIR EXCELERATE Train the Trainer
https://github.com/TrainTheTrainer/ELIXIR-EXCELERATE-TtT
https://tess.elixir-europe.org/materials/elixir-excelerate-train-the-trainer
This set of course material was designed in the context of the ELIXIR EXCELERATE Train the Trainer programme. It covers four sessions:
* Learning principles and how they apply to training and teaching
* Teaching techniques that can be used to enhance learner engagement and participation
* Lesson, course, and materials design
* Assessment and feedback in training and teaching
Allegra Via
Patricia Palagi
Pedro Fernandes
Sarah Morgan
Train the trainer, Pedagogy, Course development, Course design
Trainers
Training instructors
Training Designers
teachers
Single cell RNA-seq data analysis with Chipster
This course introduces single cell RNA-seq data analysis methods, tools and file formats. It covers the preprocessing steps of DropSeq data from raw reads to a digital gene expression matrix (DGE), and how to find sub-populations of cells using clustering with the Seurat tools. You will also...
Scientific topics: RNA-Seq
Keywords: RNA-Seq, Single Cell technologies, scRNA-seq
Resource type: course materials, Video
Single cell RNA-seq data analysis with Chipster
https://chipster.csc.fi/manual/courses.html#single-cell
https://tess.elixir-europe.org/materials/single-cell-rna-seq-data-analysis-with-chipster-6cc8f0fb-1c92-444b-ab19-b04fe6454430
This course introduces single cell RNA-seq data analysis methods, tools and file formats. It covers the preprocessing steps of DropSeq data from raw reads to a digital gene expression matrix (DGE), and how to find sub-populations of cells using clustering with the Seurat tools. You will also learn how to compare two samples and detect conserved cluster markers and differentially expressed genes in them. The user-friendly Chipster software is used in the exercises, so no Unix or R experience is required and the course is thus suitable for everybody.
Eija Korpelainen
Maria Lehtivaara
Eija Korpelainen
RNA-Seq
RNA-Seq, Single Cell technologies, scRNA-seq
Biologists
bioinformaticians
InterMine user tutorial
A tutorial for end users of InterMine
Keywords: Data querying, Data analysis, Data download, FAIR
Resource type: Tutorial
InterMine user tutorial
https://figshare.com/articles/InterMine_training_slides/4737313
https://tess.elixir-europe.org/materials/intermine-user-tutorial
A tutorial for end users of InterMine
Rachel Lyne
Yo Yehudi
Julie Sullivan
Data querying, Data analysis, Data download, FAIR
Life Science Researchers
Bioinformaticians
InterMine user manual
Documentation for end users on how to search for data, run simple and complex queries, analyse results and download data from any instance of InterMine.
Keywords: Data querying, data visualization, Data download, FAIR
Resource type: Documentation
InterMine user manual
http://flymine.readthedocs.io/en/latest
https://tess.elixir-europe.org/materials/intermine-user-manual
Documentation for end users on how to search for data, run simple and complex queries, analyse results and download data from any instance of InterMine.
Rachel Lyne
Julie Sullivan
Gos Micklem
Sergio Contrino
Yo Yehudi
Daniela Butano
Justin Clark-Casey
Data querying, data visualization, Data download, FAIR
Life Science Researchers
Bioinformaticians
InterMine operator manual
Documentation on how to install, configure and operate an InterMine instance.
Keywords: Data integration, Data analysis, Data publishing, FAIR
Resource type: Documentation
InterMine operator manual
http://intermine.readthedocs.io/en/latest
https://tess.elixir-europe.org/materials/intermine-operator-manual
Documentation on how to install, configure and operate an InterMine instance.
Julie Sullivan
Gos Micklem
Yo Yehudi
Sergio Contrino
Rachel Lyne
Daniela Butano
Justin Clark-Casey
Kevin Herald Reierskog
Data integration, Data analysis, Data publishing, FAIR
Bioinformaticians
software engineers
Informatics on High-Throughput Sequencing Data 2018 Module 6-De Novo Assmebly
Course covers the bioinformatics tools available for managing and interpreting high-throughput sequencing data, where the focus is on Illumina reads although information is applicable to all sequencer reads.
Informatics on High-Throughput Sequencing Data 2018 Module 6-De Novo Assmebly
https://bioinformaticsdotca.github.io/htseq_2018
https://tess.elixir-europe.org/materials/informatics-on-high-throughput-sequencing-data-2018-module-6-de-novo-assmebly
Course covers the bioinformatics tools available for managing and interpreting high-throughput sequencing data, where the focus is on Illumina reads although information is applicable to all sequencer reads.
Jared Simpson
Researchers
Post-Doctoral Fellows
Biologists, Genomicists, Computer Scientists
Graduate students
Informatics on High-Throughput Sequencing Data 2018 Module 1-Introduction to High-Throughput Sequencing
Course covers the bioinformatics tools available for managing and interpreting high-throughput sequencing data, where the focus is on Illumina reads although information is applicable to all sequencer reads.
Informatics on High-Throughput Sequencing Data 2018 Module 1-Introduction to High-Throughput Sequencing
https://bioinformaticsdotca.github.io/htseq_2018
https://tess.elixir-europe.org/materials/informatics-on-high-throughput-sequencing-data-2018-module-1-introduction-to-high-throughput-sequencing
Course covers the bioinformatics tools available for managing and interpreting high-throughput sequencing data, where the focus is on Illumina reads although information is applicable to all sequencer reads.
Jared Simpson
Researchers
Graduate students
Post-Doctoral Fellows
Biologists, Genomicists, Computer Scientists
Bioinformatics for Cancer Genomics 2018 Module 5-Genome Assembly
Course covers the key bioinformatics concepts and tools required to analyze cancer genomic data sets and access and work with data sets in the cloud.
Bioinformatics for Cancer Genomics 2018 Module 5-Genome Assembly
https://bioinformaticsdotca.github.io/bicg_2018
https://tess.elixir-europe.org/materials/bioinformatics-for-cancer-genomics-2018-module-5-genome-assembly
Course covers the key bioinformatics concepts and tools required to analyze cancer genomic data sets and access and work with data sets in the cloud.
Jared Simpson
Researchers
Graduate students
Biologists, Genomicists, Computer Scientists
Post-Doctoral Fellows
Bioinformatics for Cancer Genomics 2018 Module 4-Genome Alignment
Course covers the key bioinformatics concepts and tools required to analyze cancer genomic data sets and access and work with data sets in the cloud.
Bioinformatics for Cancer Genomics 2018 Module 4-Genome Alignment
https://bioinformaticsdotca.github.io/bicg_2018
https://tess.elixir-europe.org/materials/bioinformatics-for-cancer-genomics-2018-module-4-genome-alignment
Course covers the key bioinformatics concepts and tools required to analyze cancer genomic data sets and access and work with data sets in the cloud.
Jared Simpson
Researchers
Graduate students
Biologists, Genomicists, Computer Scientists
Post-Doctoral Fellows
How to install and load the Identifier Mapping Service with data needed for gene-to-variant and variant-to-gene
Tutorial describing how a BridgeDb Identifier Mapping Database (IMS) service can be started and used for gene-variant mapping.
Scientific topics: Genetic variation, Genomics
Resource type: Tutorial
How to install and load the Identifier Mapping Service with data needed for gene-to-variant and variant-to-gene
https://bigcat-um.github.io/BridgeDbVariantDatabase/Local_BridgeDb_IMS_installation.html
https://tess.elixir-europe.org/materials/how-to-install-and-load-the-identifier-mapping-service-with-data-needed-for-gene-to-variant-and-variant-to-gene
Tutorial describing how a BridgeDb Identifier Mapping Database (IMS) service can be started and used for gene-variant mapping.
Friederike Ehrhart
Jonathan Mélius
Egon Willighagen
Genetic variation
Genomics
Biologists
Bioinformatics for Cancer Genomics 2017 Module 3-Genome Alignment and Assembly
Course covers the bioinformatics tools required to analyze genomic data sets.
Bioinformatics for Cancer Genomics 2017 Module 3-Genome Alignment and Assembly
https://bioinformaticsdotca.github.io//bicg_2017
https://tess.elixir-europe.org/materials/bioinformatics-for-cancer-genomics-2017-module-3-genome-alignment-and-assembly
Course covers the bioinformatics tools required to analyze genomic data sets.
Jared Simpson
Researchers
Graduate students
Biologists, Genomicists, Computer Scientists
Post-Doctoral Fellows
Informatics on High-Throughput Sequencing Data 2017 Module 6-De Novo Assembly
Course covers the bioinformatics tools available for managing and interpreting high-throughput sequencing data with a focus on Illumina reads.
Informatics on High-Throughput Sequencing Data 2017 Module 6-De Novo Assembly
https://bioinformaticsdotca.github.io/htseq_2017
https://tess.elixir-europe.org/materials/informatics-on-high-throughput-sequencing-data-2017-module-6-de-novo-assembly
Course covers the bioinformatics tools available for managing and interpreting high-throughput sequencing data with a focus on Illumina reads.
Jared Simpson
Researchers
Graduate Students
Post-Doctoral Fellows
Biologists, Genomicists, Computer Scientists
Informatics on High-Throughput Sequencing Data 2017 Module 1-Introduction to High-Throughput Sequencing
Course covers the bioinformatics tools available for managing and interpreting high-throughput sequencing data with a focus on Illumina reads.
Informatics on High-Throughput Sequencing Data 2017 Module 1-Introduction to High-Throughput Sequencing
https://bioinformaticsdotca.github.io/htseq_2017
https://tess.elixir-europe.org/materials/informatics-on-high-throughput-sequencing-data-module-1-introduction-to-high-throughput-sequencing
Course covers the bioinformatics tools available for managing and interpreting high-throughput sequencing data with a focus on Illumina reads.
Jared Simpson
Researchers
Graduate students
Biologists, Genomicists, Computer Scientists
Post-Doctoral Fellows
High-Throughput Biology 2017 Module 6-De Novo Assembly
Course covers the key bioinformatics concepts and tools required to analyze DNA- and RNA- sequence reads using a reference genome.
High-Throughput Biology 2017 Module 6-De Novo Assembly
https://bioinformaticsdotca.github.io/high-throughput_biology_2017
https://tess.elixir-europe.org/materials/high-throughput-biology-2017-module-6-de-novo-assembly
Course covers the key bioinformatics concepts and tools required to analyze DNA- and RNA- sequence reads using a reference genome.
Jared Simpson
Researchers
Graduate students
Biologists, Genomicists, Computer Scientists
Post-Doctoral Fellows
High-Throughput Biology 2017 Module 1-Introduction to High-Throughput Sequencing
Course covers the key bioinformatics concepts and tools required to analyze DNA- and RNA- sequence reads using a reference genome.
High-Throughput Biology 2017 Module 1-Introduction to High-Throughput Sequencing
https://bioinformaticsdotca.github.io/high-throughput_biology_2017
https://tess.elixir-europe.org/materials/high-throughput-biology-2017-module-1-introduction-to-high-throughput-sequencing
Course covers the key bioinformatics concepts and tools required to analyze DNA- and RNA- sequence reads using a reference genome.
Jared Simpson
Graduate students
Post-Doctoral Fellows
Researchers
Biologists, Genomicists, Computer Scientists
Data Manipulation - Collections: Multisample Analysis
A collection of microtutorials explaining data manipulation within Galaxy
Data Manipulation - Collections: Multisample Analysis
http://galaxyproject.github.io/training-material/topics/galaxy-data-manipulation/tutorials/processing-many-samples-at-once/tutorial.html
https://tess.elixir-europe.org/materials/data-manipulation-collections-multisample-analysis
A collection of microtutorials explaining data manipulation within Galaxy
nekrut
pajanne
Data Manipulation - Collections: Using dataset collection
A collection of microtutorials explaining data manipulation within Galaxy
Questions of the tutorial:
- How to manipulate large numbers of datasets at once?
Objectives of the tutorial:
- Understand and master dataset collections
Data Manipulation - Collections: Using dataset collection
http://galaxyproject.github.io/training-material/topics/galaxy-data-manipulation/tutorials/collections/tutorial.html
https://tess.elixir-europe.org/materials/data-manipulation-collections-using-dataset-collection
A collection of microtutorials explaining data manipulation within Galaxy
Questions of the tutorial:
- How to manipulate large numbers of datasets at once?
Objectives of the tutorial:
- Understand and master dataset collections
nekrut
User Interface and Features - Histories: Understanding Galaxy history system
A collection of microtutorials explaining various features of the Galaxy user interface
Questions of the tutorial:
- How do Galaxy histories work?
Objectives of the tutorial:
- Gain understanding on navigating and manipulating histories
User Interface and Features - Histories: Understanding Galaxy history system
http://galaxyproject.github.io/training-material/topics/galaxy-ui/tutorials/history/tutorial.html
https://tess.elixir-europe.org/materials/user-interface-and-features-histories-understanding-galaxy-history-system
A collection of microtutorials explaining various features of the Galaxy user interface
Questions of the tutorial:
- How do Galaxy histories work?
Objectives of the tutorial:
- Gain understanding on navigating and manipulating histories
nekrut
Assembly - Making sense of a newly assembled genome
DNA sequence data has become an indispensable tool for Molecular Biology & Evolutionary Biology. Study in these fields now require a genome sequence to work from. We call this a 'Reference Sequence.' We need to build a reference for each species. We do this by Genome Assembly. De novo Genome...
Assembly - Making sense of a newly assembled genome
http://galaxyproject.github.io/training-material/topics/assembly/tutorials/ecoli_comparison/tutorial.html
https://tess.elixir-europe.org/materials/assembly-making-sense-of-a-newly-assembled-genome
DNA sequence data has become an indispensable tool for Molecular Biology & Evolutionary Biology. Study in these fields now require a genome sequence to work from. We call this a 'Reference Sequence.' We need to build a reference for each species. We do this by Genome Assembly. De novo Genome Assembly is the process of reconstructing the original DNA sequence from the fragment reads alone.
Questions of the tutorial:
- I just assembled a genome. How does it compare with already sequenced genomes?
- How do I find rearranged, inserted, or deleted regions?
Objectives of the tutorial:
- Identification of the most closely related genome to my new assembly
- Perform sequence comparison to locate rearrangements
- Identify genes located in deletions
nekrut
delphine-l