Pavlo Lutsik

A general team for the EOSC4Cancer project.

This workflow supports processing of bulk ACT-Seq data from raw reads to genome-wide accessiblity tracks (bigWig) and ACT-Seq peaks. The main steps include read trimming using trimGalore, alignment with bowtie2, coverage generation using samtools and peak calling with MACS2.

This workflow supports processing of bulk CUT'N'RUN data from raw reads to genome-wide accessiblity tracks (bigWig) and CUT'N'RUN peaks. The main steps include read trimming using trimGalore, alignment with bowtie2, coverage generation using samtools and peak calling with MACS2.

This workflow supports primary processing of ChIP-Seq data from raw reads to genome-wide ChIP signal tracks and ChIP peaks. The main steps include read trimming using trimGalore, alignment with bowtie2, coverage generation using samtools and peak calling with MACS2.

This workflow supports processing of bulk ATAC-Seq data from raw reads to genome-wide accessiblity tracks (bigWig) and ATAC peaks. The main steps include read trimming using trimGalore, alignment with bowtie2, coverage generation using samtools and peak calling with MACS2.

Collection of CWL worflows for various epigenomic data types, including DNA methylation, chromatin accessibility and chromatin marks (ChIP-seq, Cut'n'Run, ACT-Seq).