--- title: "lncRNA Discovery Workflow" author: "Zach Bengtsson" date: "2023-05-05" output: html_document --- ```{r setup, include=FALSE} knitr::opts_chunk$set(echo = TRUE) ``` ### HISAT2 build to create an index for the Pver_genome_assembly_v1.0.fasta file... ```{bash, eval = FALSE, echo = TRUE} /home/shared/hisat2-2.2.1/hisat2-build \ -f ../data/Pver_genome_assembly_v1.0.fasta \ ../output/Pver_genome_assembly_v1.0-valid.index ``` ### HISAT2 to align paired-end RNA-Seq reads to the Pver_genome_assembly_v1.0.fasta index... ```{bash, eval = FALSE, echo = TRUE} find /home/shared/8TB_HDD_01/pver/*gz \ | xargs basename -s _R1_001.fastq.gz | xargs -I{} \ /home/shared/hisat2-2.2.1/hisat2 \ -x ../output/Pver_genome_assembly_v1.0-valid.index \ -p 8 \ -1 /home/shared/8TB_HDD_01/pver/{}_R1_001.fastq.gz \ -2 /home/shared/8TB_HDD_01/pver/{}_R2_001.fastq.gz \ -S /home/shared/8TB_HDD_01/pver/hisat-output/{}-valid.sam ``` ### Samtools to convert the SAM files output from the previous HISAT2 command into sorted BAM files... ```{bash, eval = FALSE, echo = TRUE} for file in /home/shared/8TB_HDD_01/pver/hisat-output/*-valid.sam; do base=$(basename "$file" -valid.sam) /home/shared/samtools-1.12/samtools view -bS "$file" | \ /home/shared/samtools-1.12/samtools sort \ -o /home/shared/8TB_HDD_01/pver/samtools-output/"$base"_valid_sorted.bam done ``` ### StringTie to assemble transcripts from the sorted BAM files generated by the previous Samtools commands... ```{bash, eval = FALSE, echo = TRUE} find /home/shared/8TB_HDD_01/pver/samtools-output/*bam \ | xargs basename -s -valid_sorted.bam | xargs -I{} \ /home/shared/stringtie-2.2.1.Linux_x86_64/stringtie \ -p 8 \ -G ../data/Pver_genome_assembly_v1.0-valid.gtf \ -o /home/shared/8TB_HDD_01/pver/stringtie-output/{}-valid.gtf \ /home/shared/8TB_HDD_01/pver/samtools-output/{}-valid_sorted.bam \ ``` ### Use StrignTie merge to merge all the individual GTF files into a single merged GTF file... ```{bash, eval = FALSE, echo = TRUE} /home/shared/stringtie-2.2.1.Linux_x86_64/stringtie \ --merge \ -G ../data/Pver_genome_assembly_v1.0-valid.gtf \ -o /home/shared/8TB_HDD_01/pver/stringtie-merge-output/stringtie_merged.gtf \ /home/shared/8TB_HDD_01/pver/stringtie-output/*-valid.gtf ``` ### Use gffcompare to compare annotation file generated by StringTie to a reference annotation file and to produce a set of output files summarizing the results of the comparison, including classification of each transcript... ```{bash, eval = FALSE, echo = TRUE} /home/shared/gffcompare-0.12.6.Linux_x86_64/gffcompare \ -r ../data/Pver_genome_assembly_v1.0-valid.gtf \ -G ../data/Pver_genome_assembly_v1.0-valid.gtf \ -o /home/shared/8TB_HDD_01/pver/gffcompare-output/gffcompare_merged \ /home/shared/8TB_HDD_01/pver/stringtie-merge-output/stringtie_merged.gtf \ ``` ```{bash, eval = FALSE, echo = TRUE} awk '$3 == "transcript" && $1 !~ /^#/ {print}' /home/shared/8TB_HDD_01/pver/gffcompare-output/gffcompare_merged.annotated.gtf | grep 'class_code "u"' | awk '$5 - $4 > 199 {print}' > /home/shared/8TB_HDD_01/pver/filter-output/merged_lncRNA_candidates.gtf ``` ```{bash, eval = FALSE, echo = TRUE} /home/shared/bedtools2/bin/bedtools \ getfasta -fi ../data/Pver_genome_assembly_v1.0.fasta -bed /home/shared/8TB_HDD_01/pver/filter-output/merged_lncRNA_candidates.gtf -fo /home/shared/8TB_HDD_01/pver/bedtools-output/merged_lncRNA_candidates.fasta -name -split ``` ```{bash, eval = FALSE, echo = TRUE} eval "$(/opt/anaconda/anaconda3/bin/conda shell.bash hook)" python /home/shared/CPC2_standalone-1.0.1/bin/CPC2.py -i /home/shared/8TB_HDD_01/pver/bedtools-output/merged_lncRNA_candidates.fasta -o ~/github/zach-lncRNA/output/merged_cpc2_results ``` ```{bash, eval = FALSE, echo = TRUE} # Filter out transcripts with coding potential awk '$8 == "noncoding" {print $1}' ~/github/zach-lncRNA/output/merged_cpc2_results.txt > ~/github/zach-lncRNA/output/noncoding_transcripts_ids.txt grep -Fwf ~/github/zach-lncRNA/output/noncoding_transcripts_ids.txt /home/shared/8TB_HDD_01/pver/bedtools-output/merged_lncRNA_candidates.fasta > ~/github/zach-lncRNA/output/merged_final_lncRNAs.gtf ```