WebFeb 24, 2024 · The text was updated successfully, but these errors were encountered: WebMar 24, 2024 · Actually, you can use the bash shell hack < (gunzip -c filename.gz) to pass the gzipped file (or similarly, any other kind of zip file), which doesn't have a built-in mechanism to read the zipped files directly (STAR is awesome in providing the built-in mechanism :). It uses a trick of shell called Process Substitution.
Exercise 1. From Fastq data files to Read Count Matrix - Cornell …
WebApr 26, 2024 · Please edit the original post. Take out the extraneous info noted by @h.mon below and make sure the complete command is posted there. WebMay 6, 2024 · 要映射序列文件的名称(带路径),注如果文件是压缩的文件使用readFilesCommand参数进行解压缩。如果是(*.gz)使用 --readFilesCommand zcat或 - … gb 13544–2011
Aligning RNA-seq reads with STAR (Complete tutorial)
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 the same result. If I perform decompression first and then pass in the uncompressed fastq files everything appears to work as expected. I have confirmed that zcat and gzip work as ... 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., … WebNov 1, 2024 · readFilesCommand - Notes on how to process the read files (in this case use zcat to unzip them) readFilesIn - The forward and reverse reads; outSAMtype - Type of … gb 13540