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Ham Suçlama Geçmiş

高置信位点的整合

一、流程

二、模块

1. 选择被所有callset支持的SNVs和Indels

http://choppy.3steps.cn/renluyao/HCC_Select_HF_mutations.git

2.从VCF文件和bam文件中提取SNVs和Indel信息

4. Extract SNPs and Indels information

(1) Separate the SNVs and Indels

vcftools --gzvcf sample.filtered.normed.vcf.gz --remove-indels --recode --recode-INFO-all --out sample.filtered.normed.snv

vcftools --gzvcf sample.filtered.normed.vcf.gz --keep-only-indels  --recode --recode-INFO-all --out sample.filtered.normed.indel

rtg bgzip sample.filtered.normed.snv.vcf
rtg index sample.filtered.normed.snv.vcf.gz

rtg bgzip sample.filtered.normed.indel.vcf
rtg index sample.filtered.normed.indel.vcf.gz

(2) Separate training and testing vcf files

rtg vcffilter -i sample.filtered.normed.snv.vcf.gz -o sample.filtered.normed.snv.train.vcf.gz --include-vcf=all.filtered.vcf.gz

rtg vcffilter -i sample.filtered.normed.snv.vcf.gz -o sample.filtered.normed.snv.test.vcf.gz --exclude-vcf=all.filtered.vcf.gz

rtg vcffilter -i sample.filtered.normed.indel.vcf.gz -o sample.filtered.normed.indel.train.vcf.gz --include-vcf=all.filtered.vcf.gz

rtg vcffilter -i sample.filtered.normed.indel.vcf.gz -o sample.filtered.normed.indel.test.vcf.gz --exclude-vcf=all.filtered.vcf.gz

(3) Extract the information from VCF file

gzip -d sample.filtered.normed.snv.train.vcf.gz
gzip -d sample.filtered.normed.snv.test.vcf.gz
gzip -d sample.filtered.normed.indel.train.vcf.gz
gzip -d sample.filtered.normed.indel.test.vcf.gz

python extract_vcf_information.py -i sample.filtered.normed.snv.train.vcf -o sample.filtered.normed.snv.train.txt
python extract_vcf_information.py -i sample.filtered.normed.snv.test.vcf -o sample.filtered.normed.snv.test.txt
python extract_vcf_information.py -i sample.filtered.normed.indel.train.vcf -o sample.filtered.normed.indel.train.txt
python extract_vcf_information.py -i sample.filtered.normed.indel.train.vcf -o sample.filtered.normed.indel.train.txt

（4）Extract the information from bam-readcount

## get bed
# snv
cat sample.filtered.normed.snv.train.vcf | sed '/^#/d' | awk '{print $1"\t"$2"\t"$2"\t"$4"\t"$5}' > sample.filtered.normed.snv.train.bed

cat sample.filtered.normed.snv.test.vcf | sed '/^#/d' | awk '{print $1"\t"$2"\t"$2"\t"$4"\t"$5}' > sample.filtered.normed.snv.test.bed
#indel
python bed_for_bamReadcount.py -i sample.filtered.normed.indel.train.vcf -o sample.filtered.normed.indel.train

python bed_for_bamReadcount.py -i sample.filtered.normed.indel.test.vcf -o sample.filtered.normed.indel.test

## bam-readcount
#snv
bam-readcount -f reference.fa -l sample.filtered.normed.snv.train.bed sample.bam -b 20> sample.filtered.normed.snv.train.readcount

bam-readcount -f reference.fa -l sample.filtered.normed.snv.test.bed sample.bam -b 20 > sample.filtered.normed.snv.test.readcount

#indel
bam-readcount -f reference.fa -l sample.filtered.normed.indel.train.bed sample.bam -i -b 20 > sample.filtered.normed.indel.train.readcount

bam-readcount -f reference.fa -l sample.filtered.normed.indel.test.bed sample.bam -i -b 20 > sample.filtered.normed.indel.test.readcount

(5) Parse bam-readcount information and combine with vcf information

# add alt in to bam-readcount
awk 'NR==FNR{a[$1,$2]=$5;next} ($1,$2) in a{print $0, a[$1,$2]}' OFS="\t" sample.filtered.normed.indel.train.bed sample.filtered.normed.indel.train.readcount > sample.filtered.normed.indel.train.bamReadcount

awk 'NR==FNR{a[$1,$2]=$5;next} ($1,$2) in a{print $0, a[$1,$2]}' OFS="\t" sample.filtered.normed.indel.test.bed sample.filtered.normed.indel.test.readcount > sample.filtered.normed.indel.test.bamReadcount

awk 'NR==FNR{a[$1,$2]=$5;next} ($1,$2) in a{print $0, a[$1,$2]}'  OFS="\t" sample.filtered.normed.snv.train.bed sample.filtered.normed.snv.train.readcount > sample.filtered.normed.snv.train.bamReadcount

awk 'NR==FNR{a[$1,$2]=$5;next} ($1,$2) in a{print $0, a[$1,$2]}'  OFS="\t" sample.filtered.normed.snv.test.bed sample.filtered.normed.snv.test.readcount > sample.filtered.normed.snv.test.bamReadcount