added the pipeline script
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40c4a6ffe1
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9dbf152e31
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@ -195,14 +195,14 @@ for (var e = 0; e < exons.length; ++e) {
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}
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// drop mismapped contigs
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var dropped = [];
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for (var c = 0; c < ca.length; ++c) {
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var min = 0x7fffffff, cc = ca[c];
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for (var g = 0; g < ga.length; ++g) {
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var gg = ga[g];
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min = min < sc[gg][cc]? min : sc[gg][cc];
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for (var k = 0; k < ca.length; ++k) {
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var min = 0x7fffffff, c = ca[k];
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for (var i = 0; i < ga.length; ++i) {
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var g = ga[i];
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min = min < sc[g][c]? min : sc[g][c];
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}
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dropped[cc] = min > drop_thres? true : false;
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if (dropped[cc]) warn("Dropped contig " +clist[cc]+ " due to high divergence to all genes (minNM=" +min+ ")");
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dropped[c] = min > drop_thres? true : false;
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if (dropped[c]) warn("Dropped contig " +clist[c]+ " due to high divergence to all genes (minNM=" +min+ ")");
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}
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// fill the pair array
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var min_nm = 0xffff;
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@ -211,7 +211,7 @@ for (var e = 0; e < exons.length; ++e) {
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for (var j = i; j < ga.length; ++j) {
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var gj = ga[j], g2 = sc[gj], m = 0;
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for (var k = 0; k < ca.length; ++k) {
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c = ca[k];
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var c = ca[k];
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if (!dropped[c])
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m += g1[c] < g2[c]? g1[c] : g2[c];
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}
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@ -0,0 +1,19 @@
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#!/bin/bash
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if [ $# -lt 2 ]; then
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echo "Usage: $0 <prefix> <gene>"
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exit 1
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fi
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root=`dirname $0`
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pre=$1.$2
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len=`$root/seqtk comp $pre.fq | awk '{++x;y+=$2}END{printf("%.0f\n", y/x)}'`
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$root/fermi2.pl unitig -t2 -l$len -p $pre.utg $pre.fq > $pre.utg.mak
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make -f $pre.utg.mak
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$root/bwa mem -B1 -O1 -E1 $root/HLA-ALT.fa $pre.utg.mag.gz | grep -v ^@ | sort -k3,3 -k4,4n | bgzip > $pre.utg.alt.gz
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$root/tabix -Bpsam $pre.utg.alt.gz $root/HLA-approx.anno | cut -f1 | sort | uniq | $root/seqtk subseq $pre.utg.mag.gz - | gzip -1 > $pre.utg.fq.gz
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rm $pre.utg.{flt,ec,raw,pre}.* $pre.utg.mag* $pre.utg.mak $pre.utg.alt.gz
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$root/bwa index -p $pre.utg $pre.utg.fq.gz
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$root/bwa mem -aD.1 -t2 $pre.utg $root/hla.fa | egrep "^(@|$2)" > $pre.utg.sam
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rm $pre.utg.{ann,amb,bwt,sa,pac}
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