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v0.2.7

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Version 0.2.7

v0.2.6

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- Fixed: reads wrongly sometimes wrongly spanned two chromosomes (issues

philres#23)
- Match score reduced and low quality split + short inv detection
enabeld for -x ont

v0.2.5

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- Fix for long MD strings (segfault)

- Fix for LMP extension at chromosome borders (segfault)
- Dynamic linking is now default

v0.2.4

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- now reads from stdin if -q is skipped

- fixes for increasing stability
- updates and fixes for mapping ultra-long nanopore reads
(https://github.com/nickloman/massive-nanopore-silliness)
- Parameter --bam-fix added. Currently, BAM does not support reads with
> 64k cigar elements. When --bam-fix is set all reads with >64k Cigar
elements will be reported as unmapped to maintain compatibility with BAM

v0.2.3

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- Min residues check added to short read processing

- Parameter "--skip-write" added: If specified, ngmlr won't write the
reference index to disk
- Fix for non-deterministic MAPQ (Issue philres#13)
- Filtering changed to fix issue philres#12
- Primariy alignment flag fixed (issue philres#11)
- Set max length for read names to 500

v0.2.2

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- Compatibilty with (mini)conda

- SeqAn removed
- Switched from c++14 to c++11
- Option to switch off static build in CMake (-DSTATIC=OFF)

v0.2.1

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- Fixes for circular reference genomes

- Memory corruption fixed
- Filter for random short alignments added
- Dynamic programming approach for choosing best combination of mapped
segments (thanks to @bqminh)
- Alignment computation speedup with SSE instructions (thanks to
@smolkmo)
- Mapping quality computation updates
- Several memory leaks fixed
- Small duplication detection improved
- `--min-residues/-R` changed set to 25% (default). All reads that have
less than 25% mapped are reported as unmapped per default
- `--max-segments` added. Max number of segments reported for a single
read

v0.1.6

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- Docker image for building ngmlr added

- Gap decay parameter added
- Memory corruption fixed

0.1.5

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*) MD tag fixed

0.1.4

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Early beta release

0