GSE206674 eCLIP Data Processing
Publication
Seryl-tRNA synthetase promotes translational readthrough by mRNA binding and involvement of the selenocysteine incorporation machinery.Nucleic acids research (2023) — PMID 37739431
Dataset
GSE206674SerRS mediates translational readthrough of through engagement of the selenocysteine incorporation machinery
Processing Steps
Generate Jupyter Notebook-
1
Data was processed using the eCLIP pipeline and available at: http://github.com/yeolab/eclip
eCLIP -
2
Unique Molecular Identifiers (UMIs) were extracted from raw sequencing reads with umi_tools extract
UMI-tools -
3
Post-umi-extracted reads were trimmed for adapter sequences and barcode sequences (eCLIP samples) using cutadapt.
cutadapt -
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Trimmed reads were mapped against RepBase with STAR to remove reads mapping to repetitive sequences (--outFilterMultimapNmax 30 --alignEndsType EndToEnd --outFilterMultimapScoreRange 1 --outSAMmode Full --outFilterType BySJout --outSAMtype BAM Unsorted --outFilterScoreMin 10 --outReadsUnmapped Fastx --outSAMattributes All)
STAR -
5
Remaining reads were mapped to the appropriate genome build (hg19) using STAR aligner (--outFilterMultimapNmax 1 --alignEndsType EndToEnd --outFilterMultimapScoreRange 1 --outSAMmode Full --outFilterType BySJout --outSAMtype BAM Unsorted --outFilterScoreMin 10 --outReadsUnmapped Fastx --outSAMattributes All)
STAR -
6
Uniquely mapped reads were removed of PCR duplicates with umi_tools
UMI-tools -
7
Peak clusters were identified with CLIPper, available at: https://github.com/YeoLab/clipper
CLIPper -
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Clusters enriched over corresponding size-matched input (SMInput) were identified using a custom Perl script, available in the main eCLIP repository as: overlap_peakfi_with_bam.pl
eCLIP -
9
Overlapping enriched clusters (peaks) were merged with a custom perl script, available in the main eCLIP repository as: compress_l2foldenrpeakfi_for_replicate_overlapping_bedformat.pl
eCLIP -
10
Peaks that overlapped common exclusion/non-specific binding regions (available at: https://www.encodeproject.org/references/ENCSR922QVQ/) were removed with BEDtools
bedtools
Raw Source Text
Data was processed using the eCLIP pipeline and available at: http://github.com/yeolab/eclip Unique Molecular Identifiers (UMIs) were extracted from raw sequencing reads with umi_tools extract Post-umi-extracted reads were trimmed for adapter sequences and barcode sequences (eCLIP samples) using cutadapt. Trimmed reads were mapped against RepBase with STAR to remove reads mapping to repetitive sequences (--outFilterMultimapNmax 30 --alignEndsType EndToEnd --outFilterMultimapScoreRange 1 --outSAMmode Full --outFilterType BySJout --outSAMtype BAM Unsorted --outFilterScoreMin 10 --outReadsUnmapped Fastx --outSAMattributes All) Remaining reads were mapped to the appropriate genome build (hg19) using STAR aligner (--outFilterMultimapNmax 1 --alignEndsType EndToEnd --outFilterMultimapScoreRange 1 --outSAMmode Full --outFilterType BySJout --outSAMtype BAM Unsorted --outFilterScoreMin 10 --outReadsUnmapped Fastx --outSAMattributes All) Uniquely mapped reads were removed of PCR duplicates with umi_tools Peak clusters were identified with CLIPper, available at: https://github.com/YeoLab/clipper Clusters enriched over corresponding size-matched input (SMInput) were identified using a custom Perl script, available in the main eCLIP repository as: overlap_peakfi_with_bam.pl Overlapping enriched clusters (peaks) were merged with a custom perl script, available in the main eCLIP repository as: compress_l2foldenrpeakfi_for_replicate_overlapping_bedformat.pl Peaks that overlapped common exclusion/non-specific binding regions (available at: https://www.encodeproject.org/references/ENCSR922QVQ/) were removed with BEDtools Assembly: hg19 Supplementary files format and content: bigwigs contain RPM-normalized read densities of uniquely-mapped reads Supplementary files format and content: BED files contain CLIPper peak clusters. Columns 4 and 5 describe the -log10(p-value) and log2(fold) enrichment IP over corresponding SMInput.