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Name
Modified
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compleasm gene-completeness (HiFi)
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5 items
Merqury QV (HiFi)
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23 items
Flye assembly (ONT --nano-hq)
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6 items
hifiasm (HG002 chr20)
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22 items
Reference QV — ONT polished vs MG1655
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3 items
Contig-to-chromosome alignment — HiFi vs CHM13 chr20
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3 items
NanoPlot QC (ONT)
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4 items
Racon polish (ONT)
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9 items
compleasm gene-completeness (ONT polished)
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5 items
NanoFilt filter (ONT)
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4 items
Uploads
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2 items
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Apr 29, 2026 at 04:14
Apr 28, 2026
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Assemble genomes from long reads — both human-scale PacBio HiFi and bacterial-scale Oxford Nanopore — and benchmark the result properly. Drop in HiFi reads (HG002 chr20 in this demo) or ONT R10.4.1 reads (E. coli K-12 here), and the pipeline returns a contig-level assembly, a polished consensus where appropriate, and the QC numbers that actually tell you whether to trust it. Built for reference-grade assembly projects, T2T-style finishing efforts, microbial completion work, and anyone tired of getting a FASTA with no error estimate attached to it.
Which platform, what was your QV, how complete is the gene set — those are the questions, and the pipeline answers all three. HiFi data goes through hifiasm in its primary configuration. ONT data runs through Flye (--nano-hq) and is then polished by Racon over two rounds, re-aligning the raw reads to refine the consensus. Merqury delivers a reference-free quality value (QV) from k-mer concordance with the reads, and compleasm reports gene-level completeness using miniprot — faster and more honest on long-read assemblies than the older BUSCO pipeline. The output is a contigs FASTA, an assembly graph, a QV number you can quote, and a completeness percentage with the lineage labeled.
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This is the actual computational pipeline behind this project, not a mock-up or a screenshot. Every stage, parameter, log, and output shown here was produced by a real run.
- The graph is the workflow. Each node is a stage; arrows are data dependencies.
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