[med-svn] [Git][med-team/dnarrange][upstream] New upstream version 1.5.3
Andreas Tille (@tille)
gitlab at salsa.debian.org
Tue Jul 19 13:18:53 BST 2022
Andreas Tille pushed to branch upstream at Debian Med / dnarrange
Commits:
978a034b by Andreas Tille at 2022-07-19T11:58:56+02:00
New upstream version 1.5.3
- - - - -
2 changed files:
- README.md
- setup.py
Changes:
=====================================
README.md
=====================================
@@ -109,12 +109,12 @@ and [MAFFT][] to be installed).
Then
re-[align](https://github.com/mcfrith/last-rna/blob/master/last-long-reads.md)
-the merged reads to the genome (it's recommended to do this without
-repeat-masking):
+the merged reads to the genome (maybe using e.g. `-m20` or `-m50` to
+make it more sensitive-but-slow):
lastdb -P8 -uNEAR mydb genome.fa
last-train -P8 mydb merged.fa > merged.par
- lastal -P8 -p merged.par mydb merged.fa | last-split > merged.maf
+ lastal -P8 -m20 --split -p merged.par mydb merged.fa > merged.maf
And draw pictures:
@@ -266,7 +266,7 @@ You can get the rearranged reads, without merging them, like this:
dnarrange-merge all-reads.fq groups.maf > some-reads.fq
This may be useful if you wish to re-align the rearranged reads to the
-genome more slowly-and-carefully (e.g. without repeat-masking).
+genome more slowly-and-carefully.
`dnarrange-merge` also has options that it passes to `lamassemble`:
you can see them with `dnarrange-merge --help`, and they're described
=====================================
setup.py
=====================================
@@ -1,6 +1,6 @@
import setuptools
-commitInfo = " (HEAD -> master, tag: 1.5.2)".strip("( )").split()
+commitInfo = " (HEAD -> master, tag: 1.5.3)".strip("( )").split()
version = commitInfo[commitInfo.index("tag:") + 1].rstrip(",")
setuptools.setup(
View it on GitLab: https://salsa.debian.org/med-team/dnarrange/-/commit/978a034b2890501a402d6e222b5dc5ba9b645727
--
View it on GitLab: https://salsa.debian.org/med-team/dnarrange/-/commit/978a034b2890501a402d6e222b5dc5ba9b645727
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