r1237: documented -x splice:sr

This commit is contained in:
Heng Li
2025-03-30 21:47:47 -04:00
parent 4b8b4418df
commit f536b69b81
3 changed files with 15 additions and 2 deletions
+11 -1
View File
@@ -1,4 +1,4 @@
.TH minimap2 1 "12 March 2024" "minimap2-2.28 (r1209)" "Bioinformatics tools"
.TH minimap2 1 "30 March 2025" "minimap2-2.28-dirty (r1237)" "Bioinformatics tools"
.SH NAME
.PP
minimap2 - mapping and alignment between collections of DNA sequences
@@ -416,6 +416,10 @@ Score bonus when alignment extends to the end of the query sequence [0].
.BI --score-N \ INT
Score of a mismatch involving ambiguous bases [1].
.TP
.BI --pe-ind-chain
For paired-end short reads, perform chaining for each end independently.
By default, minimap2 chains the two ends together.
.TP
.BR --splice-flank = yes | no
Assume the next base to a
.B GT
@@ -682,6 +686,12 @@ Spliced alignment for accurate long RNA-seq reads such as PacBio iso-seq
.B -C5 -O6,24
.BR -B4 ).
.TP
.B splice:sr
Spliced alignment for short RNA-seq reads
.RB ( -xsplice:hq
.B --frag=yes --end-bonus=10 -2K50m --heap-sort=yes --pe-ind-chain
.BR --secondary=no ).
.TP
.B sr
Short-read alignment without splicing
.RB ( -k21