File Info

Filename
.command.out
Full Path
s3://natera-rnd-pltf-dev-nextflow-scratch-01/work/fe/7a9bad36e86c7fc45dde82b7023494/.command.out
Size
4.8 KB
Attempt
[2026-06-08T08:34:50] Launching Arriba 2.4.0
[2026-06-08T08:34:50] Loading assembly from 'ref_genome.fa' 
[2026-06-08T08:35:03] Loading annotation from 'ref_annot.gtf' 
[2026-06-08T08:35:07] Reading chimeric alignments from '659_Dd-T1-TRNA-1_B23MHV2LT4_1.Aligned.sortedByCoord.out.bam' (total=11376061)
[2026-06-08T08:42:50] Marking multi-mapping alignments (marked=6812124)
[2026-06-08T08:42:55] Detecting strandedness (reverse)
[2026-06-08T08:42:55] Assigning strands to alignments 
[2026-06-08T08:42:58] Annotating alignments 
[2026-06-08T08:43:35] Filtering duplicates (remaining=8212375)
[2026-06-08T08:43:43] Filtering mates which do not map to interesting contigs (1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 X Y AC_* NC_*) (remaining=7795856)
[2026-06-08T08:43:46] Filtering mates which only map to viral contigs (AC_* NC_*) (remaining=7795856)
[2026-06-08T08:43:48] Filtering viral contigs with expression lower than the top 5 (remaining=7795856)
[2026-06-08T08:43:54] Filtering viral contigs with less than 5% coverage (remaining=7795856)
[2026-06-08T08:43:57] Estimating fragment length (mate gap mean=-83.931, mate gap stddev=33.6544, read length mean=136.118)
[2026-06-08T08:43:57] Filtering read-through fragments with a distance <=10000bp (remaining=7397737)
[2026-06-08T08:43:59] Filtering inconsistently clipped mates (remaining=7304286)
[2026-06-08T08:44:02] Filtering breakpoints adjacent to homopolymers >=6nt (remaining=7124760)
[2026-06-08T08:44:08] Filtering fragments with small insert size (remaining=7123695)
[2026-06-08T08:44:10] Filtering alignments with long gaps (remaining=7123693)
[2026-06-08T08:44:13] Filtering fragments with both mates in the same gene (remaining=7122203)
[2026-06-08T08:44:16] Filtering fusions arising from hairpin structures (remaining=6724715)
[2026-06-08T08:44:19] Filtering reads with a mismatch p-value <=0.01 (remaining=3487503)
[2026-06-08T08:44:38] Filtering reads with low entropy (k-mer content >=60%) (remaining=1377485)
[2026-06-08T08:44:53] Finding fusions and counting supporting reads (total=973282)
[2026-06-08T08:45:14] Merging adjacent fusion breakpoints (remaining=965210)
[2026-06-08T08:45:16] Filtering multi-mapping fusions by alignment score and read support (remaining=657774)
[2026-06-08T08:45:51] Estimating expected number of fusions by random chance (e-value) 
[2026-06-08T08:45:59] Filtering fusions with both breakpoints in adjacent non-coding/intergenic regions (remaining=654958)
[2026-06-08T08:46:00] Filtering intragenic fusions with both breakpoints in exonic regions (remaining=387248)
[2026-06-08T08:46:01] Filtering fusions with <2 supporting reads (remaining=54921)
[2026-06-08T08:46:02] Filtering fusions with an e-value >=0.3 (remaining=19717)
[2026-06-08T08:46:03] Searching for internal tandem duplications <=100bp with >=10 supporting reads and >=7% allele fraction (remaining=19778)
[2026-06-08T08:46:07] Filtering fusions with both breakpoints in intronic/intergenic regions (remaining=19596)
[2026-06-08T08:46:08] Searching for known fusions in 'known_fusions_hg38_GRCh38_v2.4.0.tsv.gz' (remaining=19625)
[2026-06-08T08:46:10] Filtering in vitro-generated fusions between genes with an expression above the 99.8% quantile (remaining=11773)
[2026-06-08T08:46:16] Searching for fusions with spliced split reads (remaining=11826)
[2026-06-08T08:46:21] Selecting best breakpoints from genes with multiple breakpoints (remaining=5527)
[2026-06-08T08:46:23] Filtering read-through fusions with breakpoints near the gene boundary (remaining=5473)
[2026-06-08T08:46:24] Searching for fusions with >=4 spliced events (remaining=6722)
[2026-06-08T08:46:26] Filtering blacklisted fusions in 'blacklist_hg38_GRCh38_v2.4.0.tsv.gz' (remaining=2442)
[2026-06-08T08:46:47] Filtering fusions with anchors <=23nt (remaining=1639)
[2026-06-08T08:46:47] Filtering end-to-end fusions with low support (remaining=1601)
[2026-06-08T08:46:48] Filtering fusions with no coverage around the breakpoints (remaining=1574)
[2026-06-08T08:46:49] Indexing gene sequences 
[2026-06-08T08:46:55] Filtering genes with >=30% identity (remaining=475)
[2026-06-08T08:46:59] Re-aligning chimeric reads to filter fusions with >=80% mis-mappers (remaining=223)
[2026-06-08T08:47:04] Selecting best breakpoints from genes with multiple breakpoints (remaining=194)
[2026-06-08T08:47:06] Searching for additional isoforms (remaining=251)
[2026-06-08T08:47:07] Assigning confidence scores to events 
[2026-06-08T08:47:11] Loading protein domains from 'protein_domains_hg38_GRCh38_v2.4.0.gff3'
[2026-06-08T08:47:11] Writing fusions to file '659_Dd-T1-TRNA-1_B23MHV2LT4_1.arriba.fusions.tsv' 
[2026-06-08T08:47:14] Writing discarded fusions to file '659_Dd-T1-TRNA-1_B23MHV2LT4_1.arriba.fusions.discarded.tsv'
[2026-06-08T08:47:49] Freeing resources
[2026-06-08T08:48:07] Done (elapsed time=00:13:17, CPU time=00:13:16, peak memory=16.1gb)