Releases
v3.15.0
Features
Issue key
Summary
NIR-574
Update OMIM
NIR-569
Update ClinVar
NIR-540
Add command-line arguments to the Downloader for changing S3 URLs and manifest filenames
NIR-520
Add support for identifying in-frame gene fusions
NIR-495
Port bidirectional allele trimmer fix for breakend locations when using legacy VID mode
NIR-494
Port legacy VID fixes from 3.6.x
NIR-480
Add support for INV3/INV5 tags with respect to gene fusions
NIR-477
Add support for FusionCatcher data sources
NIR-474
Add support for COSMIC gene fusions
NIR-459
Update HGVS g. notation for MT variants to use m. notation
NIR-324
Allow masked reference bases in PAR regions (chrY)
NIR-257
Update Nirvana to use gnomAD 3.1 for GRCh38
NIR-250
Update the BlockCompression library
NIR-193
Add support for detecting out of disk space issues in Downloader
Bugs fixed
Issue key
Summary
NIR-548
Nirvana incorrectly recomposes an deletion and assigns a negative genotype
NIR-398
Mito Heteroplasmy not using trimmed and left-aligned alt alleles for annotation
NIR-214
Nirvana doesn't support regular gzip VCF file
NIR-213
Downloader unintentionally removes genomic reference file
Unresolved bugs
Issue key
Summary
NIR-602
SAUtils CustomVar won't allow missing values for Score columns
NIR-582
Jasix incorrectly closes the JSON header when combining query with header
NIR-504
SingleAnnotation behaves differently in Lambda vs REST API
NIR-220
Nirvana doesn't use the transcript sequence to report the reference amino acids in HGVS p. notations
NIR-219
Nirvana reports ambiguous protein level annotations for CUG start codon variants
NIR-218
Duplicates may be marked as insertions in HGVS
NIR-217
Nirvana produces HGVS insertions notations that are more than one bp apart
NIR-215
Nirvana incorrectly determines gnomAD low complexity regions at translocation breakend boundaries
NIR-212
Annotation lambdas run out of disk space when large amounts of CA are submitted
NIR-91
Nirvana should fully right align duplications in HGVS c. notation
NIR-87
Nirvana should detect duplications in HGVS by looking at the transcript sequence.
NIR-86
Nirvana incorrectly handles insertions where RNA-edit insertions already occur
NIR-75
Nirvana doesn't handle 3' UTR intron HGVS c. notation properly
NIR-57
Nirvana produces bizarre HGVS p. notation (NP_001137434.1:p.(Val701_?_fsTer?))
NIR-56
CDS position goes beyond the CDS sequence length (NM_001300952.1)
NIR-55
Nirvana produces a strange CDS position range for NM_001346067.1
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