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r190: default -k to 15; added -x map-ont
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+47
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@@ -1,4 +1,4 @@
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.TH minimap2 1 "18 July 2017" "minimap2-2.0-r180-dirty" "Bioinformatics tools"
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.TH minimap2 1 "19 July 2017" "minimap2-2.0-r190-dirty" "Bioinformatics tools"
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.SH NAME
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.PP
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minimap2 - mapping and alignment between collections of DNA sequences
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@@ -74,7 +74,7 @@ SAM format.
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.SS Indexing options
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.TP 10
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.BI -k \ INT
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Minimizer k-mer length [17]
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Minimizer k-mer length [15]
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.TP
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.BI -w \ INT
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Minimizer window size [2/3 of k-mer length]. A minimizer is the smallest k-mer
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@@ -164,35 +164,6 @@ secondary alignments [5]. This option has no effect when
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.B -X
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is applied.
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.TP
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.BI -x \ STR
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Preset []. This option applies multiple options at the same time. It should be
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applied before other options because options applied later will overwrite the
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values set by
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.BR -x .
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Available
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.I STR
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are:
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.RS
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.TP 8
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.B ava-pb
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PacBio all-vs-all overlap mapping (-Hk19 -w5 -Xp0 -m100 -K500m -g10000 --max-chain-skip 25)
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.TP 8
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.B ava-ont
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Oxford Nanopore all-vs-all overlap mapping (-k15 -w5 -Xp0 -m100 -K500m -g10000 --max-chain-skip 25)
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.TP
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.B map10k
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PacBio/Oxford Nanopore read to reference mapping (-Hk19)
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.TP
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.B asm5
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Long assembly to reference mapping (-k19 -w19 -A1 -B19 -O39,81 -E3,1 -s200 -z200).
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Typically, the alignment will not extend to regions with 5% or higher sequence
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divergence. Only use this preset if the average divergence is far below 5%.
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.TP
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.B asm10
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Long assembly to reference mapping (-k19 -w19 -A1 -B9 -O16,41 -E2,1 -s200 -z200). Up
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to 10% sequence divergence.
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.RE
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.TP
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.BI --max-chain-skip \ INT
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A heuristics that stops chaining early [50]. Minimap2 uses dynamic programming
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for chaining. The time complexity is quadratic in the number of seeds. This
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@@ -265,6 +236,51 @@ use
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.TP
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.B -V
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Print version number to stdout
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.SS Preset options
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.TP 10
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.BI -x \ STR
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Preset []. This option applies multiple options at the same time. It should be
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applied before other options because options applied later will overwrite the
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values set by
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.BR -x .
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Available
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.I STR
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are:
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.RS
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.TP 8
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.B map-pb
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PacBio/Oxford Nanopore read to reference mapping (-Hk19)
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.TP
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.B map10k
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The same as
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.B map-pb
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(-Hk19)
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.TP
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.B map-ont
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Slightly more sensitive for Oxford Nanopore to reference mapping (-k15). For
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PacBio reads, HPC minimizers consistently leads to faster performance and more
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sensitive results in comparison to normal minimizers. For Oxford Nanopore data,
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normal minimizers are better, though not much. The effectiveness of HPC is
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determined by the sequencing error mode.
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.TP
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.B asm5
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Long assembly to reference mapping (-k19 -w19 -A1 -B19 -O39,81 -E3,1 -s200 -z200).
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Typically, the alignment will not extend to regions with 5% or higher sequence
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divergence. Only use this preset if the average divergence is far below 5%.
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.TP
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.B asm10
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Long assembly to reference mapping (-k19 -w19 -A1 -B9 -O16,41 -E2,1 -s200 -z200). Up
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to 10% sequence divergence.
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.TP 8
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.B ava-pb
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PacBio all-vs-all overlap mapping (-Hk19 -w5 -Xp0 -m100 -K500m -g10000 --max-chain-skip 25)
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.TP 8
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.B ava-ont
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Oxford Nanopore all-vs-all overlap mapping (-k15 -w5 -Xp0 -m100 -K500m -g10000
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--max-chain-skip 25). Similarly, the major difference from
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.B ava-pb
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is that this preset is not using HPC minimizers.
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.RE
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.SS Miscellaneous options
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.TP 10
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.B --no-kalloc
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