hisatgenotype_locus.py --aligner-list hisat2.graph --base hla --locus-list A --num-editdist 2 --assembly -1 ILMN/NA12892.extracted.1.fq.gz -2 ILMN/NA12892.extracted.2.fq.gz

   for i in `ls -l CP_80/LP*1.fq.gz | awk '{print $NF}' | cut -d'/' -f2 | cut -d'.' -f1`; do echo $i; ./hisatgenotype_locus.py --locus-list A --num-editdist 2 --assembly --reads CP_80/$i.extracted.1.fq.gz,CP_80/$i.extracted.2.fq.gz --assembly-base assembly_graph_$i 2> $i.tmp; done

   hisatgenotype_locus_samples.py -p 3 -v --max-sample 400 --region-list hla.A --read-dir CP_400 --out-dir test_A > cp_400_A.txt
   hisatgenotype_scripts/compare_HLA_Omixon.py cp_400_A.txt ../CAAPA/omixon_caapa_hla.txt

   hisatgenotype_locus.py --aligner-list hisat2.graph --locus-list A --num-editdist 2 --assembly -1 CP_80/LP6005106-DNA_H02.extracted.fq.1.gz -2 CP_80/LP6005106-DNA_H02.extracted.fq.2.gz --display-alleles A*23:17,A*02:02:01:01

   hisatgenotype_extract_reads.py --base-fname genotype_genome --reference-type genome --read-dir ILMN_12062016 --out-dir ILMN

   hisat2 --no-hd -x genotype_genome -c CAGCTGGGATGTGGAGTGGTGTGAGGAGTGGCCACAGGGGAGCAGAGGAGGTGGCAGAAGCCGGAGGTAAAGGTGTCTTAAA


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