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update README
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@@ -22,7 +22,7 @@ outputs consist of:
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somatic mutations and recurrent sequencing errors.
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2. Haplotype-resolved processed unitig graph without small bubbles
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(*prefix*.p\_utg.gfa). Small bubbles might be caused by somatic mutations or noise in data,
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which are not the real haplotype information
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which are not the real haplotype information.
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3. Primary assembly [contig][unitig] graph (*prefix*.p\_ctg.gfa). This graph collapses different
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haplotypes.
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4. Alternate assembly contig graph (*prefix*.a\_ctg.gfa). This graph consists of all assemblies that
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@@ -40,8 +40,7 @@ For trio assembly, the input of hifiasm is the PacBio Hifi reads in fasta/fastq
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In addition, hifiasm also outputs three binary files that save all overlap inforamtion
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(*prefix*.ec.bin, *prefix*.ovlp.reverse.bin, *prefix*.ovlp.source.bin). With these files, hifiasm can avoid the time-consuming all-to-all overlap calculation step, and do the assembly
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In addition, hifiasm also outputs three binary files that save all overlap information (*prefix*.ec.bin, *prefix*.ovlp.reverse.bin, *prefix*.ovlp.source.bin). With these files, hifiasm can avoid the time-consuming all-to-all overlap calculation step, and do the assembly
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directly and quickly. This might be helpful when you want to get an optimized
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assembly by multiple rounds of experiments with different parameters.
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