splicemutr is a tool for evaluating how individual splice junctions affect coding transcripts from RNAseq data.
STAR: 2.7.3a R: 4.0.2
The fastq files were aligned using the following command:
STAR --genomeDir $GENOME_DIR --readFilesIn ${fastq1} ${fastq2} --twopassMode Basic --outSAMstrandField intronMotif --outFileNamePrefix $outprefix --runThreadN 6 --readFilesCommand zcat --outSAMtype BAM Unsorted
STAR outputs high confidence junction files as well as BAM files. These junction files must be converted to filetypes appropriate for the next steps in the splicemutr pipeline. This is done in the following way, using the associated script file:
splicemute/scripts/STAR_to_leaf.R -o $OUT -s $STAR_FILE
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