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improved manuscript
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@@ -58,7 +58,7 @@ in v2.19 through v2.22 to improve mapping results.
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\section{Methods}
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\subsection{Rescuing high-occurrence $k$-mers}
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Minimap2 keeps all $k$-mer minimizers during indexing. Its original
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Minimap2 keeps all $k$-mer minimizers~\citep{Roberts:2004fv} during indexing. Its original
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implementation only selected low-occurrence minimizers during mapping. The
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cutoff is a few hundred for mapping long reads against a human genome. If a
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read habors only a few or even no low-occurrence minimizers, it will fail
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@@ -77,12 +77,14 @@ time by a few percent on real data.
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\subsection{Aligning through longer INDELs}
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The original minimap2 may fail to align long INDELs due to its chaining
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heuristics. Briefly, minimap2 applies dynamic programming (DP) to chain
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minimizer anchors. This is a quadratic algorithm, which is slow for chaining
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minimizer anchors. This is a quadratic algorithm, slow for chaining
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contigs. For acceptable performance, the original minimap2 uses a 500bp band by
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default. If there is an INDEL longer than 500bp and the two chains around the INDEL
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default, which means a gap longer than 500bp will stop chaining.
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To align through longer gaps, older minimap2 implemented a long-join heurstic as follows.
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If there is an INDEL longer than 500bp and the two chains around the INDEL
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have no overlaps on either the query or the reference sequence, minimap2 may
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join the two short chains later at a later step. We call it the
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long-join heuristic. This heuristic may fail around VNTRs because short chains
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join the two short chains later.
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This heuristic may fail around VNTRs because short chains
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often have overlaps in VNTRs. More subtly, minimap2 may escape the inner DP
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loop early, again for performance, if the chaining result is not improved for
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50 iterations. When there is a copy number change in a long segmental
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@@ -90,13 +92,13 @@ duplication, the early escape may break around the event even if users
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specify a large band.
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In minigraph~\citep{Li:2020aa}, we developed a new chaining algorithm that
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finds short INDELs with DP-based chaining and goes through long INDELs with a
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finds up to 1kb INDELs with DP-based chaining and goes through longer INDELs with a
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subquadratic algorithm~\citep{DBLP:conf/wabi/AbouelhodaO03}. We ported the same
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algorithm to minimap2 for contig mapping. For long-read mapping, the minigraph
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algorithm is slower. Minimap2 v2.22 now still uses the DP-based algorithm to
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algorithm is slower. Minimap2 v2.22 still uses the DP-based algorithm to
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find short chains and then invokes the minigraph algorithm to rechain anchors in
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these short chains. The rechaining step achieves the same goal as long-join
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but is more reliable as it can resolve overlaps between short chains. The old
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but is more reliable because it can resolve overlaps between short chains. The old
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long-join heuristic has since been removed.
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\subsection{Properly mapping long reads with SVs}
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@@ -108,23 +110,23 @@ algorithm.
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In our view, this problem is rooted in impropriate scoring: affine-gap penalty
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over-penalizes a long INDEL that was often evolutionarily created in one event.
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We should not penalize a SV linearly in its length. Minimap2 v2.22 rescores
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We should not penalize a SV by a function linear in the SV length. Minimap2 v2.22 instead rescores
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an alignment with the following scoring function. Suppose an alignment consists
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of $M$ matching bases, $N$ substitutions and $G$ gap opens, we empirically
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score the alignment with
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$$
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M-\frac{N+G}{2d}-\sum_{i=1}^G\log_2(1+g_i)
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S=M-\frac{N+G}{2d}-\sum_{i=1}^G\log_2(1+g_i)
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$$
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where $g_i\ge1$ is the length of the $i$-th gap and
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$$
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d=\max\left\{\frac{N+G}{M+N+G},0.02\right\}
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$$
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Here $d$ approximates per-base sequence divergence with the smallest value set
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It approximates per-base sequence divergence except with the smallest value set
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to 2\%. As an analogy to affine-gap scoring, the matching score in our scheme
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is 1, the mismatch and gap open penalties are both $1/2d$ and the gap extension
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penalty is a logarithm function of the gap length. Our scoring gives a long SV
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a much milder penalty. In terms of time complexity, scoring an alignment is
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linear in the length of the alignment. Time spent on rescoring is negligible in
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linear in the length of the alignment. The time spent on rescoring is negligible in
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practice.
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%If we assume sequences evolve under a duplication-mutation model, we may have a
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@@ -159,11 +161,11 @@ $[$real-sv-1k$]$ \% false discovery rate & 2.7 & {\bf 2.4} & 2.7 & N/A \\
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10 or higher were evaluated by ``paftools.js mapeval''. The mapping error rate
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is measured in the phred scale: if the error rate is $e$, $-10\log_{10}e$ is
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reported in the table. In $[$winno-cmp$]$, 1.39 million CHM13 HiFi reads from
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SRR11292121 were mapped against CHM13. 99.3\% of them were mapped by Winnowmap2
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SRR11292121 were mapped against the same CHM13 assembly. 99.3\% of them were mapped by Winnowmap2
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at mapping quality 10 or higher and were taken as ground truth to evaluate
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minimap2 and lra with ``paftools.js pafcmp''. $[$sim-sv$]$ simulated 1,000
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50bp to 1000bp INDELs from chr8 in CHM13 using SURVIVOR~\citep{Jeffares:2017aa} and simulated Nanopore
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reads at 30 folds with the same pbsim2 command line. SVs were called with
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reads at 30-fold coverage with the same pbsim2 command line. SVs were called with
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``sniffles -q 10''~\citep{Sedlazeck:2018ab} and compared to the simulated truth with ``SURVIVOR eval
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call.vcf truth.bed 50''. In $[$real-sv-1k$]$, small and long variants were
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called by dipcall-0.3~\citep{Li:2018aa} for HG002 assemblies (AC: GCA\_018852605.1 and
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@@ -178,25 +180,27 @@ quality 10 or higher (mapQ10). However, it may occasionally assign a high mappin
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quality to a read with multiple identical best alignments. This reduced its
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mapping accuracy.
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In lack of groud truth for real data, so we took Winnowmap2 mapping as ground
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truth to evaluate other mappers (winno-cmp). Out of 1,378,092 reads with mapQ10
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In lack of groud truth for real data, we took Winnowmap2 mapping as ground
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truth to evaluate other mappers (winno-cmp in Table~\ref{tab:1}). Out of 1,378,092 reads with mapQ10
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alignments by Winnowmap2, minimap2 v2.22 could map all of them. 118 reads, less
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than 0.01\% of all reads, were mapped differently by v2.22. 51 of them have
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multiple identical best alignments. We believe these are more likely to be
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Winnowmap2 errors. Most of the remaining 67 (=118-51) reads have multiple
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highly similar but not identical alignments. We are not sure what are real
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mapping errors.
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highly similar but not identical alignments. We are not sure how many are real
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mapping errors. Minimap2 v2.18 is less consistent with Winnowmap2. Most of the
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differences are located in highly repetitive regions.
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The two benchmarks above only evaluate read mappings without variations.
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The two benchmarks above only evaluate read mappings when there are no variations between the reads and the reference.
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To measure the mapping accuracy in the presence of SVs (sim-sv), we reproduced
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the results by~\citep{Jain2020.11.01.363887}. Minimap2 v2.22 is as good as
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Winnowmap2 now. Note that we were setting the Sniffles mapping quality
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threshold to 10 in consistent with the benchmarks above. If we used the
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default threshold 20, v2.22 would miss additional 0.5\% SVs, suggesting
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minimap2 v2.22 could map variant reads correctly but with conservative mapping
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quality. This observation is more about the interaction between mappers and
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callers. Furthermore, the simulation here only considers a simple scenario in
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evolution. Non-allelic gene conversions, which happen often in segmental
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default threshold 20, v2.22 would miss additional five SVs (accounting for
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0.5\% of simulated SVs). For four out of these missing five SVs, minimap2 v2.22
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mapped more variant reads than Winnowmap2. Sniffles did not call these SVs
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because minimap2 tended to give them conservative mapping quality. It is worth
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noting that the simulation here only considers a simple scenario in evolution.
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Non-allelic gene conversions, which happen often in segmental
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duplications~\citep{Harpak:2017aa}, would obscure the optimal mapping
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strategies. How much such simple SV simulation informs real-world SV calling
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remains a question.
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@@ -205,8 +209,8 @@ To see if minimap2 v2.22 could improve long INDEL alignment, we ran dipcall on
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contig-to-reference alignments and focused on INDELs longer than 1kb
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(real-sv-1k). v2.22 is more sensitive at comparable specificity, confirming its
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advantage in more contiguous alignment. lra is supposed to handle long INDELs
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better, too. However, we could not get lra to work well with dipcall, so did
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not report the numbers.
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well, too. However, we could not get dipcall to work well with lra,
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so did not report the numbers.
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Minimap2 spends most computing time on base alignment. As recent improvements
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in v2.22 incur little additional computing and do not change the base alignment
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@@ -215,7 +219,7 @@ consistently faster than Winnowmap2 by several times. Sometimes simple
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heuristics can be as effective as more sophisticated yet slower solutions.
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\section*{Acknowledgements}
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We thank Arang Rhie and Chirag Jain for providing motivating examples where
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We thank Arang Rhie and Chirag Jain for providing motivating examples for which
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older minimap2 underperforms.
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\paragraph{Funding\textcolon} This work is funded by NHGRI grant R01HG010040.
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