The bug is primarily related to salmon (bulk mode)Describe the bug
Version Info: This is the most recent version of salmon.
# salmon (alignment-based) v0.14.1
# [ program ] => salmon
# [ command ] => quant
# [ libType ] => { U }
# [ alignments ] => { Analysis/Quantification/OJ33.sam }
# [ targets ] => { Analysis/Pinfish/corrected_transcriptome_polished_collapsed.fas }
# [ output ] => { Analysis/Quantification/OJ33 }
# [ noErrorModel ] => { }
# [ writeUnmappedNames ] => { }
Logs will be written to Analysis/Quantification/OJ33/logs
[2019-08-13 11:13:43.563] [jointLog] [info] Fragment incompatibility prior below threshold. Incompatible fragments will be ignored.
Library format { type:single end, relative orientation:none, strandedness:unstranded }
[2019-08-13 11:13:43.563] [jointLog] [info] numQuantThreads = 4
parseThreads = 4
Checking that provided alignment files have consistent headers . . . done
Populating targets from aln = "Analysis/Quantification/OJ33.sam", fasta = "Analysis/Pinfish/corrected_transcriptome_polished_collapsed.fas" . . .done
[2019-08-13 11:13:46.239] [jointLog] [info] replaced 1 non-ACGT nucleotides with random nucleotides
processed 2000000 reads in current roundSegmentation fault (core dumped)
To Reproduce
Which version of salmon was used?
salmon 0.14.1
How was salmon installed (compiled, downloaded executable, through bioconda)?
downloaded executable
Which reference was used?
custom, transcriptom derived from nanopore long-reads using Pinfish pipeline
Which read files were used?
SAM file returned by minimap2 (nanopore long reads)
Which which program options were used?salmon quant -l U -a Analysis/Quantification/OJ33.sam -t Analysis/Pinfish/corrected_transcriptome_polished_collapsed.fas -o Analysis/Quantification/OJ33 --noErrorModel --writeUnmappedNames > Analysis/Quantification/OJ33.logDesktop (please complete the following information):
x86_64 GNU/Linux
The bug is primarily related to salmon (bulk mode) Describe the bug
To Reproduce
Which version of salmon was used? salmon 0.14.1 How was salmon installed (compiled, downloaded executable, through bioconda)? downloaded executable Which reference was used? custom, transcriptom derived from nanopore long-reads using Pinfish pipeline Which read files were used? SAM file returned by minimap2 (nanopore long reads) Which which program options were used?
salmon quant -l U -a Analysis/Quantification/OJ33.sam -t Analysis/Pinfish/corrected_transcriptome_polished_collapsed.fas -o Analysis/Quantification/OJ33 --noErrorModel --writeUnmappedNames > Analysis/Quantification/OJ33.log
Desktop (please complete the following information): x86_64 GNU/Linux