minia 3.2.6-1 source package in Ubuntu
Changelog
minia (3.2.6-1) unstable; urgency=medium [ Steffen Moeller ] * New upstream version * debhelper-compat 13 (routine-update) * Adjusted build dependencies to patched version of gatb 1.4.2 * d/rules - improved clean * d/watch - using regular releases again (up from 3.2.1 to 3.2.4) [ Vagrant Cascadian ] * Do not embed kernel version in binary to enable reproducible builds Closes: #998420 [ Andreas Tille ] * Fix watchfile to detect new versions on github * New upstream version * Standards-Version: 4.6.0 (routine-update) -- Andreas Tille <email address hidden> Fri, 12 Nov 2021 09:35:16 +0100
Upload details
- Uploaded by:
- Debian Med
- Uploaded to:
- Sid
- Original maintainer:
- Debian Med
- Architectures:
- any
- Section:
- misc
- Urgency:
- Medium Urgency
See full publishing history Publishing
Series | Published | Component | Section | |
---|---|---|---|---|
Jammy | release | universe | misc |
Downloads
File | Size | SHA-256 Checksum |
---|---|---|
minia_3.2.6-1.dsc | 2.1 KiB | f2484088c7364ae673ad16bb6cf0ddeb6e5c91438b13c956ef54a78aa44b6fab |
minia_3.2.6.orig.tar.gz | 1.0 MiB | a201c5b479092617259cb1d5e0f0045b80c106e8e2aa9afe4834b4d3dd39ce78 |
minia_3.2.6-1.debian.tar.xz | 16.8 KiB | 0d77477018ef45cfd12244cbf9d6070a12dbf7bd16f3ec033acc6cd2bf3e68ab |
Available diffs
No changes file available.
Binary packages built by this source
- minia: short-read biological sequence assembler
What was referred to as "next-generation" DNA sequencing up to
the year 2020 delivered only "short" reads up to ~600 base pairs
in length that would then have to be puzzled by random overlaps
in their sequence towards a complete genome. This is the genome
assembly. And there are many biological pitfalls on long stretches
of low complexity regions and copy number variations and other
sorts of redundancies that render this difficult.
.
This package provides a short-read DNA sequence assembler based on a
de Bruijn graph, capable of assembling a human genome on a desktop
computer in a day.
.
The output of Minia is a set of contigs, i.e. stretches of gap-free
linear overlaps of short reads. In the best possible case this is
a whole chromosome.
.
Minia produces results of similar contiguity and accuracy to other
de Bruijn assemblers (e.g. Velvet).
- minia-dbgsym: debug symbols for minia