動画検索
関連広告
検索結果
intro
install tools using conda
download sequence reads using wget
download the reference genome using your browser
download the reference genome using python
trim the raw reads using sickle
index the reference genome using bwa index command
genome mapping using bwa
convert the sam file to bam file using samtools
sort the bam file using samtools
map and sort using a one liner command
get the mapping statistics using samtools
get the converage information for bases and calculate genotype likelyhoods
call variants using bcftools
post-vcf analysis using bcftools
intro and pc requirement
download the example data
index the VCF file
get the list of chromosomes
save the chromosome list to an output file.
count the variants per chromosome
include chromosomes to count
exclude chromosomes
automate the counting process
create a bash script to count all variants per chromosome