Hi Nirmalya and Zhen,
I have analyzed my own ChIP-seq data (from FASTQ to Peak calling) and now I want to use MAnorm to do normalization on my dataset.
I have the same question as this: I can't figure out what the "sample1_readfile.bed" is?
Is it the alignment file obtained after mapping to the genome (SAM/BAM)?
The example files in the MAnorm download don't have more details either:
sample1_peaks.bed (has 1000 lines) and is of the following format:
chr start end
sample1_reads.bed (has 10000 lines) and is of the following format:
How do we generate the sample1_reads.bed file?
Thanks!
Mayuri
Graduate student
Suite 203, Two Biotech
University of Massachusetts Medical School
373 Plantation St.
Worcester, MA 01605