This lecture will unite the last lecture’s content on genomic analysis with our previous coding in R. The packages we’ll use this week are from Bioconductor, a collection of software specifically designed for genomic analysis in R.
Genome variant analysis (Background)
Genomic Data (hands-on tutorials)
We will be working through some tutorials directly on your laptop using R Studio.
## start R session ##
R
## run this command within R session ##
source("../../software/genomic_data.R")
Rsamtools: querying BAM filesVariantAnnotation: reading VCF filesGenomicRanges: manipulating genomic dataplyranges: fast & easy tool for mannipulating GRangeslecture16) containing the following three RMarkdown tutorials:
Extensions (on left panel) > Type in search bar: "R Extension" > Select R Extension for Visual Studio Code by Yuki Uedapandocpandoc.pandoc outside of VScode by downloading the installer here: https://pandoc.org/installing.htmllecture16 directory. The files should have the following filenames:
BRCA.genome_wide_snp_6_broad_Level_3_scna.segBRCA_IDC_cfDNA.bamBRCA_IDC_cfDNA.bam.baiGIAB_highconf_v.3.3.2.vcf.gz (if this file was automatically uncompressed on your computer, resulting in a file named GIAB_highconf_v.3.3.2.vcf, look in your Trash folder to find the original file ending in gz)GIAB_highconf_v.3.3.2.vcf.gz.tbi