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r296: expose splicing related options to CLI
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+17
-10
@@ -1,4 +1,4 @@
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.TH minimap2 1 "12 August 2017" "minimap2-2.0-r290-dirty" "Bioinformatics tools"
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.TH minimap2 1 "13 August 2017" "minimap2-2.0-r296-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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@@ -205,6 +205,18 @@ the contiguity of the alignment at the cost of poor alignment in the middle
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Minimal peak DP alignment score to output [40]. The peak score is computed from
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the final CIGAR. It is the score of the max scoring segment in the alignment
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and may be different from the total alignment score.
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.TP
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.BI -u \ CHAR
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How to find canonical splicing sites GT-AG -
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.BR f :
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transcript strand;
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.BR b :
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both strands;
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.BR n :
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no attempt to match GT-AG [n]
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.TP
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.BI --cost-non-gt-ag \ INT
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Cost of non-canonical splicing sites [0].
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.SS Input/output options
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.TP 10
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.B -Q
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@@ -302,11 +314,10 @@ is that this preset is not using HPC minimizers.
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.B splice
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Long-read spliced alignment
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.RB ( -k15
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.B -w5 --splice -g2000 -G200k -A1 -B2 -O2,32 -E1,0
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.BR -z200 ).
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As of now, minimap2 only finds approximate exon boundaries. The true boundaries
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are usually within 10bp around the reported positions. In the splice mode,
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1) long deletions are taken as introns and represented as the
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.B -w5 --splice -g2000 -G200k -A1 -B2 -O2,32 -E1,0 -z200 -ub --cost-non-gt-ag
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.BR 4 ).
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In the splice mode, 1) long deletions are taken as introns and represented as
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the
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.RB ` N '
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CIGAR operator; 2) long insertions are disabled; 3) deletion and insertion gap
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costs are different during chaining; 4) the computation of the
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@@ -387,10 +398,6 @@ Minimap2 does not work well with Illumina short reads as of now.
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*
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Minimap2 requires SSE2 instructions to compile. It is possible to add
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non-SSE2 support, but it would make minimap2 slower by several times.
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.TP
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*
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In the splice mode, minimap2 is unable to find the precise exon boundaries.
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The true bounraries are usually within 10bp around the reported locations.
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.SH SEE ALSO
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.PP
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miniasm(1), minimap(1), bwa(1).
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