added two bowtie2 numbers for comparison
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@ -543,16 +543,17 @@ in minimap2 in future.
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To evaluate the accuracy of minimap2 on real data, we aligned human reads
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To evaluate the accuracy of minimap2 on real data, we aligned human reads
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(AC:ERR1341796) with BWA-MEM and minimap2, and called SNPs and small INDELs
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(AC:ERR1341796) with BWA-MEM and minimap2, and called SNPs and small INDELs
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with GATK HaplotypeCaller v3.5~\citep{Depristo:2011vn}. This run was sequenced
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with GATK HaplotypeCaller v3.5~\citep{Depristo:2011vn}. This run was sequenced
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from experimentally mixed CHM1 and CHM13 cell lines. Both them are homozygous
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from experimentally mixed CHM1 and CHM13 cell lines. Both of them are homozygous
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across the whole genome and have been \emph{de novo} assembled with SMRT reads
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across the whole genome and have been \emph{de novo} assembled with SMRT reads
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to high quality. This allowed us to construct an independent truth variant
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to high quality. This allowed us to construct an independent truth variant
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data set
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data set
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(\href{https://github.com/lh3/CHM-eval}{https://github.com/lh3/CHM-eval}) for
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(\href{https://github.com/lh3/CHM-eval}{https://github.com/lh3/CHM-eval}) for
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ERR1341796. In this evaluation, minimap2 has higher SNP false negative rate
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ERR1341796. In this evaluation, minimap2 has higher SNP false negative rate
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(FNR; 2.5\% of minimap2 vs 2.2\% of BWA-MEM), but fewer false positive SNPs per
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(FNR; 2.5\% of minimap2 vs 2.2\% of BWA-MEM), but fewer false positive SNPs per
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million bases (FPPM; 3.0 vs 3.9), lower INDEL FNR (7.3\% vs 7.5\%) and similar
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million bases (FPPM; 3.0 vs 3.9), lower 2--50bp INDEL FNR (7.3\% vs 7.5\%) and
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INDEL FPPM (both 1.0). The difference between the two mappers is much smaller
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similar INDEL FPPM (both 1.0). In comparison, Bowtie2 has a SNP FNR of 4.7\%
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than between BWA-MEM and Bowtie2.
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and INDEL FNR of 10.4\%. Minimap2 is broadly similar to BWA-MEM in the context
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of small variant calling.
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\section{Conclusion}
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\section{Conclusion}
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