https://github.com/bioconductor/biocasiapacific2015
Workshop and other material for BiocAsiaPacific activities in Tokyo, September 7-9 2015
Science Score: 13.0%
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Low similarity (10.4%) to scientific vocabulary
Repository
Workshop and other material for BiocAsiaPacific activities in Tokyo, September 7-9 2015
Basic Info
- Host: GitHub
- Owner: Bioconductor
- Language: R
- Default Branch: devel
- Size: 45.5 MB
Statistics
- Stars: 1
- Watchers: 7
- Forks: 0
- Open Issues: 0
- Releases: 0
Metadata Files
README.md
Course Google-doc
Last-minute instructions are available on the course google doc, active before and during the course.
To start using an AMI, visit https://courses.bioconductor.org/ .
Abstract
DNA sequence analysis generates large volumes of data that present challenging bioinformatic and statistical problems. This tutorial introduces established and new Bioconductor packages and workflows for analyzing sequence data. The Bioconductor project (http://bioconductor.org) is a widely used collection of nearly 1000 R packages for high-throughput genomic analysis. Approaches for efficiently manipulating sequences and alignments and other common work flows will be covered along with the unique statistical challenges associated with 'RNAseq', variant annotation and other experiments. The emphasis is on exploratory analysis, and the analysis of designed experiments. The workshop will touch on the Biostrings, ShortRead, GenomicRanges, DESeq2, VariantAnnotation, and other packages, with short exercises to illustrate the functionality of each package.
Goals
Gain overall familiarity with Bioconductor packages for high-throughput sequence analysis, including Bioconductor vignettes and classes.
Obtain experience running bioinformatic workflows for data quality assessment, RNA-seq differential expression, and manipulating variant call format files.
Appreciate the importance of ranges and range-based manipulation for modern genomic analysis
Learn 'best practices' for working with large data
Outline (tentative!)
Time | Topic ----------------- | ---------------------------------------------------------------------------- 10:00am - 10:15am | Welcome & Overview (Course Overview & AMI set-up) 10:20am - 11:00am | Introduction: Analysis and Comprehension of High Throughput Genomic Data 11:05am - 12:00pm | Sequences, Alignments, and Large Data 12:00pm - 1:00pm | Lunch, Divercity (15 mins walk from AIST) 1:00pm - 2:00pm | RNA-Seq Known-gene Differential Expression 2:05pm - 3:00pm | Gene, Genome, and Variant Annotation 3:00pm - 3:30pm | Coffee break, Espresso Americano (Telecom Center, 5 mins walk from AIST) 3:30pm - 4:00pm | Topic ??? / Bring your own data 4:05pm - 4:15pm | Feedback
Prerequisites
The workshop assumes an intermediate level of familiarity with R, and basic understanding of biological and technological aspects of high-throughput sequence analysis. Participants should come prepared with a modern wireless-enabled laptop and web browser installed.
Installation
Follow these steps:
- Install R version 3.2.2 from https://cran.r-studio.com
Install the Bioconductor installer
source("https://bioconductor.org/biocLite.R")Install the course package and depedencies
biocLite("devtools") biocLite("Bioconductor/BiocAsiaPacific2015", dependencies=TRUE)
Intended Audience:
This workshop is for professional bioinformaticians and statisticians intending to use R/Bioconductor for analysis and comprehension of high-throughput sequence data.
Reference
Huber et al. (2015) Orchestrating high-throughput genomic analysis with Bioconductor. Nature Methods. Jan 29;12(2):115-21.
Owner
- Name: Bioconductor
- Login: Bioconductor
- Kind: organization
- Website: https://bioconductor.org
- Repositories: 156
- Profile: https://github.com/Bioconductor
Software for the analysis and comprehension of high-throughput genomic data
GitHub Events
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Last Year
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Last synced: about 1 year ago
All Time
- Total issues: 0
- Total pull requests: 1
- Average time to close issues: N/A
- Average time to close pull requests: 4 months
- Total issue authors: 0
- Total pull request authors: 1
- Average comments per issue: 0
- Average comments per pull request: 0.0
- Merged pull requests: 1
- Bot issues: 0
- Bot pull requests: 0
Past Year
- Issues: 0
- Pull requests: 0
- Average time to close issues: N/A
- Average time to close pull requests: N/A
- Issue authors: 0
- Pull request authors: 0
- Average comments per issue: 0
- Average comments per pull request: 0
- Merged pull requests: 0
- Bot issues: 0
- Bot pull requests: 0
Top Authors
Issue Authors
Pull Request Authors
- katrinleinweber (1)
Top Labels
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Dependencies
- BiocInstaller * imports
- AnnotationHub * suggests
- BSgenome.Hsapiens.UCSC.hg19 * suggests
- BiocParallel * suggests
- BiocStyle * suggests
- Biostrings * suggests
- DESeq2 * suggests
- GenomicAlignments * suggests
- GenomicFiles * suggests
- GenomicRanges * suggests
- Gviz * suggests
- Homo.sapiens * suggests
- IRanges * suggests
- RNAseqData.HNRNPC.bam.chr14 * suggests
- Rsamtools * suggests
- TxDb.Hsapiens.UCSC.hg19.knownGene * suggests
- VariantAnnotation * suggests
- airway * suggests
- biomaRt * suggests
- ggplot2 * suggests
- knitr * suggests
- org.Hs.eg.db * suggests
- rtracklayer * suggests
- shiny * suggests
- BiasedUrn * imports