この方法は個人使用のみを目的としています。!
# 进入conda环境
conda activate genome_feature
# 安装
conda install -c bioconda quast
quast.pyを実行します
mkdir quast && cd quast
# NOTICE: Genes are not predicted by default. Use --gene-finding or --glimmer option to enable it.
# WARNING: GeneMark tool can't be started because of license limitations!
# so 选择--glimmer
quast.py ../3.15188_genome.fasta --fungus --glimmer -t 8 -o 3.15188
QUASTの結果
# 结果文件
report.txt summary table
report.tsv tab-separated version, for parsing, or for spreadsheets (Google Docs, Excel, etc)
report.tex Latex version
report.pdf PDF version, includes all tables and plots for some statistics
report.html everything in an interactive HTML file
icarus.html Icarus main menu with links to interactive viewers
contigs_reports [only if a reference genome is provided]
misassemblies_report detailed report on misassemblies
unaligned_report detailed report on unaligned and partially unaligned contigs
k_mer_stats [only if --k-mer-stats is specified]
kmers_report detailed report on k-mer-based metrics
reads_stats [only if reads are provided]
reads_report detailed report on mapped reads statistics
総合的な結果については、report.html Web ページを参照してください。写真とデータが含まれており、report.txt が主要なデータです。
# 得到如下重要内容
# contigs 16
Largest contig 4508325
Total length 34000033
GC (%) 48.49
N50 3074509
N90 1550349
auN 2916380.1
L50 5
L90 12
バッチ実行
# pep70
for i in `cat /media/aa/DATA/SZQ2/bj/functional_annotation/70list.txt`
do
echo "quast.py /media/aa/DATA/SZQ2/bj/a.preparing_data/genome_unmasked_fasta_data/$i.genome.fasta --fungus --glimmer -t 8 -o $i"
done > command.quast.list
ParaFly -c command.quast.list -CPU 48
# pepmy
for i in `cat /media/aa/DATA/SZQ2/bj/functional_annotation/pepmylist.txt`
do
echo "quast.py /media/aa/DATA/SZQ2/bj/a.preparing_data/genome_unmasked_fasta_data/$i.genome.fasta --fungus --glimmer -t 8 -o $i"
done > command.quast2.list
ParaFly -c command.quast2.list -CPU 48