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README.md

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@@ -76,19 +76,20 @@ impg query -p alignments.paf -r chr1:1000-2000 -x -m 3
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# Filter by minimum gap-compressed identity
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impg query -p alignments.paf -r chr1:1000-2000 --min-identity 0.9
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# Output formats (auto/bed/bedpe/paf/gfa/maf)
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# Output formats (auto/bed/bedpe/paf/gfa/maf/fasta)
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impg query -p alignments.paf -r chr1:1000-2000 -o bed
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impg query -p alignments.paf -r chr1:1000-2000 -o bedpe
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impg query -p alignments.paf -b regions.bed -o paf
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impg query -p alignments.paf -b chr1:1000-2000 -o paf
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# GFA/MAF/FASTA output requires sequence files (--sequence-files or --sequence-list)
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# gfa/maf/fasta output requires sequence files (--sequence-files or --sequence-list)
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impg query -p alignments.paf -r chr1:1000-2000 -o gfa --sequence-files ref.fa genomes.fa
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impg query -p alignments.paf -r chr1:1000-2000 -o maf --sequence-list fastas.txt
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impg query -p alignments.paf -r chr1:1000-2000 -o fasta --sequence-files *.fa
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# Works with AGC archives too
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impg query -p alignments.paf -r chr1:1000-2000 -o gfa --sequence-files genomes.agc
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# FASTA output with reverse complement for reverse strand sequences
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# fasta output with reverse complement for reverse strand sequences
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impg query -p alignments.paf -r chr1:1000-2000 -o fasta --sequence-files *.fa --reverse-complement
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# Merge nearby regions (default: 0)

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