diff --git a/minimap2.html b/minimap2.html
index e521044..a30e08f 100644
--- a/minimap2.html
+++ b/minimap2.html
@@ -216,20 +216,27 @@ ignore minimizers occuring more than
-xsr mode, which sets the threshold for a second round of seeding.
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-|
-map-pb |
-PacBio/Oxford Nanopore read to reference mapping
-(-Hk19) |
-|
+ |
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map-ont |
-Slightly more sensitive for Oxford Nanopore to reference mapping
-(-k15). For PacBio reads, HPC minimizers consistently leads to faster performance and
-more sensitive results in comparison to normal minimizers. For Oxford Nanopore
-data, normal minimizers are better, though not much. The effectiveness of HPC
-is determined by the sequencing error mode.
+Align noisy long reads of ~10% error rate to a reference genome. This is the
+default mode.
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-|
+ |
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+map-hifi |
+Align PacBio high-fidelity (HiFi) reads to a reference genome
+(-k19 -w19 -U50,500 -g10k -A1 -B4 -O6,26 -E2,1 -s200). |
+|
+map-pb |
+Align older PacBio continuous long (CLR) reads to a reference genome
+(-Hk19). |
+|
asm5 |
Long assembly to reference mapping
-(-k19 -w19 -A1 -B19 -O39,81 -E3,1 -s200 -z200 -N50 --min-occ-floor=100). Typically, the alignment will not extend to regions with 5% or higher sequence
+(-k19 -w19 -U50,500 --rmq -r100k -g10k -A1 -B19 -O39,81 -E3,1 -s200 -z200 -N50). Typically, the alignment will not extend to regions with 5% or higher sequence
divergence. Only use this preset if the average divergence is far below 5%.
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-|
+ |
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asm10 |
Long assembly to reference mapping
-(-k19 -w19 -A1 -B9 -O16,41 -E2,1 -s200 -z200 -N50 --min-occ-floor=100). Up to 10% sequence divergence.
+(-k19 -w19 -U50,500 --rmq -r100k -g10k -A1 -B9 -O16,41 -E2,1 -s200 -z200 -N50). Up to 10% sequence divergence.
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-|
+ |
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asm20 |
Long assembly to reference mapping
-(-k19 -w10 -A1 -B4 -O6,26 -E2,1 -s200 -z200 -N50 --min-occ-floor=100). Up to 20% sequence divergence.
+(-k19 -w10 -U50,500 --rmq -r100k -g10k -A1 -B4 -O6,26 -E2,1 -s200 -z200 -N50). Up to 20% sequence divergence.
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-|
-ava-pb |
-PacBio all-vs-all overlap mapping
-(-Hk19 -Xw5 -m100 -g10000 --max-chain-skip 25). |
-|
-ava-ont |
-Oxford Nanopore all-vs-all overlap mapping
-(-k15 -Xw5 -m100 -g10000 -r2000 --max-chain-skip 25). Similarly, the major difference from
-ava-pb is that this preset is not using HPC minimizers.
- |
-|
+ |
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splice |
Long-read spliced alignment
-(-k15 -w5 --splice -g2000 -G200k -A1 -B2 -O2,32 -E1,0 -C9 -z200 -ub --junc-bonus=9 --splice-flank=yes). In the splice mode, 1) long deletions are taken as introns and represented as
+(-k15 -w5 --splice -g2k -G200k -A1 -B2 -O2,32 -E1,0 -C9 -z200 -ub --junc-bonus=9 --cap-sw-mem=0 --splice-flank=yes). In the splice mode, 1) long deletions are taken as introns and represented as
the
N CIGAR operator; 2) long insertions are disabled; 3) deletion and insertion gap
costs are different during chaining; 4) the computation of the
ms tag ignores introns to demote hits to pseudogenes.
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-|
-splice:hq |
| |
+ |
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+splice:hq |
Long-read splice alignment for PacBio CCS reads
(-xsplice -C5 -O6,24 -B4). |
-|
+ |
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sr |
Short single-end reads without splicing
(-k21 -w11 --sr --frag=yes -A2 -B8 -O12,32 -E2,1 -r50 -p.5 -N20 -f1000,5000 -n2 -m20 -s40 -g200 -2K50m --heap-sort=yes --secondary=no). |
+|
+ava-pb |
+PacBio CLR all-vs-all overlap mapping
+(-Hk19 -Xw5 -e0 -m100). |
+|
+ava-ont |
+Oxford Nanopore all-vs-all overlap mapping
+(-k15 -Xw5 -e0 -m100 -r2k). |
|