Difference between revisions of "RV-TDT Exercise"

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(RV-TDT exercise)
 
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==RV-TDT exercise==
 
==RV-TDT exercise==
 +
 
  vtools init rvtdt
 
  vtools init rvtdt
 
  vtools import --format vcf data/data.vcf --build hg19
 
  vtools import --format vcf data/data.vcf --build hg19
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  vtools select func_variant -o chr pos refGene.name2 maf --header > vat_export.anno
 
  vtools select func_variant -o chr pos refGene.name2 maf --header > vat_export.anno
 
  # Mendelian error and recode
 
  # Mendelian error and recode
  plink --noweb --tfile vat_export --recode12 --me 1 1 --set-me-missing --out "recode12_noME"
+
  plink --noweb --tfile vat_export --me 1 1 --set-me-missing --make-bed --out "noME"
 +
plink --bfile noME --recode12 --out "recode12_noME"
 
  sort -n -k1 -k6 -k2 recode12_noME.ped | sed 's/ /\t/g' | cut -f1,3,4,5 --complement > linkage.ped
 
  sort -n -k1 -k6 -k2 recode12_noME.ped | sed 's/ /\t/g' | cut -f1,3,4,5 --complement > linkage.ped
 
  cut -f2 recode12_noME.map | awk 'BEGIN{OFS="\t";} {print "M",$0}' | sed '1i\I\tid\nA\tDisease' > linkage.dat
 
  cut -f2 recode12_noME.map | awk 'BEGIN{OFS="\t";} {print "M",$0}' | sed '1i\I\tid\nA\tDisease' > linkage.dat

Latest revision as of 17:42, 24 January 2019

RV-TDT exercise

vtools init rvtdt
vtools import --format vcf data/data.vcf --build hg19
vtools phenotype --from_file data/phen.txt
# variant selection
vtools execute ANNOVAR  geneanno
vtools select variant "variant.region_type like '%splicing%'or variant.mut_type like 'nonsynonymous%' or variant.mut_type like 'frameshift%' or variant.mut_type like 'stop%'" -t func_variant
# tped file
vtools export func_variant --format tped --samples 'phenotype is not null'  > vat_raw.tped
sort -k4 -n vat_raw.tped | awk 'BEGIN{OFS="\t";prev="None";copy=1} {$2=$1"_"$4; $3=0; if($2==prev) {$2=$2"_"copy; copy=copy+1} else {prev=$2; copy=1}; print $0}' > vat_export.tped
# tfam file
vtools phenotype --out family sample_name pid mid sex phenotype > vat_export.tfam
# anno file
vtools use refGene-hg19_20130904
vtools update func_variant --set 'maf=0.001' 
vtools select func_variant -o chr pos refGene.name2 maf --header > vat_export.anno
# Mendelian error and recode
plink --noweb --tfile vat_export --me 1 1 --set-me-missing --make-bed --out "noME"
plink --bfile noME --recode12 --out "recode12_noME"
sort -n -k1 -k6 -k2 recode12_noME.ped | sed 's/ /\t/g' | cut -f1,3,4,5 --complement > linkage.ped
cut -f2 recode12_noME.map | awk 'BEGIN{OFS="\t";} {print "M",$0}' | sed '1i\I\tid\nA\tDisease' > linkage.dat
java -Xmx10000m -jar java/linkage2beagle.jar linkage.dat linkage.ped > pre_beagle.bgl
python script/pre_phase.py -i pre_beagle.bgl -a pre_beagle_withMissing.bgl
java -Xmx10000m -jar java/beagle.jar missing=0 trios=pre_beagle.bgl out=bgl_phased verbose=false redundant=true
gunzip bgl_phased.pre_beagle.bgl.phased.gz
python script/post_phase.py -a vat_export.anno -b bgl_phased.pre_beagle.bgl.phased -o genes/
for g in `ls genes | grep tped | cut -d"." -f1 | head -20` 
do 
    echo "runing rvTDT on gene "${g}
    rvTDT exercise_proj -G ./genes/${g}.tped -P ./data/rvtdt.phen -M ./genes/${g}.map --adapt 500 --alpha 0.00001 --permut 2000 --lower_cutoff 0 --upper_cutoff 100 --minVariants 3 --maxMissRatio 1 
done 
# Answer
vtools show tables
ls genes/ | grep tped | wc
cat exercise_proj_pval/*.pval | grep -v "^#" | sort -k2
cat exercise_proj_pval/*.pval | grep -v "^#" | sort -k3
# clean
rm -r exercise_proj* genes/* bgl* linkage* recode12* pre_beagle* vat_export.*