biomystery / atacCNV

A tool to call CNV (Copy Number Variation) from bulk ATAC-Seq data
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atac-seq bioinformatics cnv

atacCNV

Call Copy Number Variation from ATAC-seq data.

Useage

export PATH=$PATH:$(pwd)

List of files

Typical Steps:

  1. Get output from pipleine: tagAlign, peaks (openning regions).
  2. (optional) Run tagToFrag.sh: get fragments bed, bdg and bw
  3. Run readsMasker.sh to filter out reads or frags in peak regions and get background frags.
  4. Run smoothBw.sh to get average coverage in each window for both control or treatment. It will reorder the bed file, so that the it cannot preserve the pair info if input is in tagAlign format. Please covert to fragment bed first.
  5. Run callCNV.R to get CNV regions, segment plots

Call Wrapper: