WebTeams. Q&A for work. Connect and share knowledge within a single location that is structured and easy to search. Learn more about Teams WebJun 24, 2015 · The resulting sam file was empty and the log file indicated that no reads were read. I have tried --readFilesCommand gzip -c and --readFilesCommand gunzip -c with …
How do I specify the number of CPU cores to use within a python …
WebMay 26, 2024 · Then, I tried to aligned the reads like this: STAR --genomeDir output/index --readFilesIn reads.fastq.gz --readFilesCommand gunzip -c --outFileNamePrefix output/alignment --quantMode GeneCounts --outSAMunmapped None --outSAMtype BAM SortedByCoordinate --outSAMattrRGline ID:RG1 CN:yy \"DS: z z z\" SM:sample WebJul 19, 2024 · It looks like it's entirely missing the quality string and sequence string. The paired end file lengths are the same and divisible by 4. Interestingly, when I run STAR on a copy of the files pre-trimming/barcode extraction (noting that the read IDs are modified slightly upon trimming and barcode extraction by removal of the sample index, i.e., … ipro scheduling
EXITING because of FATAL ERROR in reads input: quality string …
WebNov 17, 2024 · --readFilesCommand gunzip -cparameter to the above mapping command. STAR Parameters description for mapping reads to genome, If your study goal is to … WebOct 27, 2024 · Our input data is compressed in gz format, so we will use --readFilesCommand to supply STAR with the decompression method: zcat or gunzip -c. … WebOct 12, 2024 · cat ids parallel echo STAR --runThreadN 12 --genomeDir $IDX --readFilesCommand gunzip -c --readFilesIn $INP/ {}_1_trimmed.fq.gz\ --sjdbGTFfile $GTF --outFileNamePrefix $RES --limitGenomeGenerateRAM 32000000000 \ --outSAMtype BAM SortedByCoordinate > run.sh orc hit points 5e