Release minimap2-2.4 (r555)

This commit is contained in:
Heng Li
2017-11-06 12:54:02 -05:00
parent 1617b87ee1
commit 21a46ba652
6 changed files with 46 additions and 9 deletions
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@@ -1,3 +1,41 @@
Release 2.4-r555 (6 November 2017)
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As is planned, this release focuses on fine tuning the base algorithm. Notable
changes include
* Changed the mapping quality scale to match the scale of BWA-MEM. This makes
minimap2 and BWA-MEM achieve similar sensitivity-specificity balance on real
short-read data.
* Improved the accuracy of splice alignment by modeling one additional base
close to the GT-AG signal. This model is used by default with `-x splice`.
For SIRV control data, however, it is recommended to add `--splice-flank=no`
to disable this feature as the SIRV splice signals are slightly different.
* Tuned the parameters for Nanopore Direct RNA reads. The recommended command
line is `-axsplice -k14 -uf` (#46).
* Fixed a segmentation fault when aligning PacBio reads (#47 and #48). This
bug is very rare but it affects all versions of minimap2. It is also
recommended to re-index reference genomes created with `map-pb`. For human,
two minimizers in an old index are wrong.
* Changed option `-L` in sync with the final decision of hts-specs: a fake
CIGAR takes the form of `<readLen>S<refLen>N`. Note that `-L` only enables
future tools to recognize long CIGARs. It is not possible for older tools to
work with such alignments in BAM (#43 and #51).
* Fixed a tiny issue whereby minimap2 may waste 8 bytes per candidate
alignment.
The minimap2 technical note hosted at arXiv has also been updated to reflect
recent changes.
(2.4: 6 November 2017, r555)
Release 2.3-r531 (22 October 2017)
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@@ -26,7 +64,7 @@ This release come with many improvements and bug fixes:
This release has implemented all the major features I planned five months ago,
with the addition of spliced long-read alignment. The next couple of releases
will focus on fine tuning of base algorithms.
will focus on fine tuning of the base algorithms.
(2.3: 22 October 2017, r531)