Open markram4 opened 3 months ago
Copy and paste the exact command you tried to run flair collapse -g /cluster/pixstor/slotkinr-lab/mkramer/annotations/arabidopsis/At_v2/At_array.v2.RUBY.fa -q ruby_round1_merge.non_pA_all_corrected.bed -r /cluster/pixstor/slotkinr-lab/mkramer/projects/target_capture/ruby_round1/data/4_cutadapt_trim_5p_3p_adapters/5p/ruby_round1_merged.trimmed.3p.trimmed.5p.fastq --gtf /cluster/pixstor/slotkinr-lab/mkramer/annotations/arabidopsis/At_v2/At_array.v2.Arabidopsis_thaliana.TAIR10.56.targetChr.all.flair.gtf --output /cluster/pixstor/slotkinr-lab/mkramer/projects/target_capture/ruby_round1/data/6_minimap/2_map_to_capture/output/mapped_to_targets/flair/02_collapse/ruby_round1_merge.non_pA_all_corrected --generate_map --trust_ends --no_gtf_end_adjustment --max_ends 10000 --threads 8 --temp_dir /cluster/pixstor/slotkinr-lab/mkramer/projects/target_capture/tmp --keep_intermediate &
How did you install Flair? (We'd prefer it if you used one of the top two because they are the least likely to have package compatibility problems.)
conda create -n flair -c conda-forge -c bioconda flair
What happened?
Read data extracted Single-exon genes grouped, collapsing Renaming isoforms using gtf Aligning reads to first-pass isoform reference [M::mm_idx_gen::0.023*1.07] collected minimizers [M::mm_idx_gen::0.027*1.72] sorted minimizers [M::main::0.027*1.72] loaded/built the index for 819 target sequence(s) [M::mm_mapopt_update::0.028*1.70] mid_occ = 72 [M::mm_idx_stat] kmer size: 15; skip: 10; is_hpc: 0; #seq: 819 [M::mm_idx_stat::0.028*1.68] distinct minimizers: 24665 (27.88% are singletons); average occurrences: 7.179; average spacing: 5.401; total length: 956397 [M::worker_pipeline::55.314*7.42] mapped 749805 sequences [M::worker_pipeline::95.711*7.57] mapped 749823 sequences [M::worker_pipeline::137.787*7.64] mapped 730521 sequences [M::worker_pipeline::181.483*7.68] mapped 882797 sequences [M::worker_pipeline::217.464*7.69] mapped 1244651 sequences [M::worker_pipeline::268.611*7.71] mapped 1112451 sequences [M::worker_pipeline::312.232*7.72] mapped 1038374 sequences [M::worker_pipeline::356.258*7.73] mapped 1002897 sequences [M::worker_pipeline::409.759*7.73] mapped 1084268 sequences [M::worker_pipeline::464.462*7.64] mapped 1132555 sequences [M::worker_pipeline::514.777*7.65] mapped 1181024 sequences [M::worker_pipeline::770.447*5.86] mapped 1307645 sequences [M::worker_pipeline::849.144*5.81] mapped 929774 sequences Failed at counting step for isoform read support``` We know it's ugly but we promise it helps us solve problems faster. **What else do we need to know?** Go ahead, every bit helps.
Copy and paste the exact command you tried to run flair collapse -g /cluster/pixstor/slotkinr-lab/mkramer/annotations/arabidopsis/At_v2/At_array.v2.RUBY.fa -q ruby_round1_merge.non_pA_all_corrected.bed -r /cluster/pixstor/slotkinr-lab/mkramer/projects/target_capture/ruby_round1/data/4_cutadapt_trim_5p_3p_adapters/5p/ruby_round1_merged.trimmed.3p.trimmed.5p.fastq --gtf /cluster/pixstor/slotkinr-lab/mkramer/annotations/arabidopsis/At_v2/At_array.v2.Arabidopsis_thaliana.TAIR10.56.targetChr.all.flair.gtf --output /cluster/pixstor/slotkinr-lab/mkramer/projects/target_capture/ruby_round1/data/6_minimap/2_map_to_capture/output/mapped_to_targets/flair/02_collapse/ruby_round1_merge.non_pA_all_corrected --generate_map --trust_ends --no_gtf_end_adjustment --max_ends 10000 --threads 8 --temp_dir /cluster/pixstor/slotkinr-lab/mkramer/projects/target_capture/tmp --keep_intermediate &
How did you install Flair? (We'd prefer it if you used one of the top two because they are the least likely to have package compatibility problems.)
conda create -n flair -c conda-forge -c bioconda flair
)What happened?