Could you help me to understand how to analyze the data CHIP- seq paired-end on galaxy ?
Thank you.
Could you help me to understand how to analyze the data CHIP- seq paired-end on galaxy ?
Thank you.
Do you have any particular questions about the analysis, or do you just need some help getting started?
For the latter, here's an example that might help you out: https://usegalaxy.org/u/james/p/exercise-chip-seq
Hi Dannon,
I have a question about running MACS tool for my chip-seq data to call the peaks in Galaxy.
My data is pair-end sequenced. I have already upload the BAM mapping file I want to run MACS tool under the “Paired End Sequencing” but it asks for the ELANDMULTI format and for tow ChIP-seq Tag files.
How can I get the ELANDMULTI format dataset ? Do I only map each file Fastq R1 and R2 before starting MACS tool ?
Thank you
Sonia
I don't think there's actually a tool on usegalaxy.org for creating elandmulti files. The last advice I heard for this was to use the Cistrome Galaxy to create this file (http://cistrome.org/ap/root), but other than that I'm not familiar enough with this to offer much advice -- perhaps someone else can chime in here.
Hi all,
I have a question about running MACS tool for my chip-seq data to call the peaks in Galaxy.
My data is pair-end sequenced. I have already upload the BAM mapping file I want to run MACS tool under the “Paired End Sequencing” but it asks for the ELANDMULTI format and for tow ChIP-seq Tag files.
How can I get the ELANDMULTI format dataset ? Do I only map each file Fastq R1 and R2 before starting MACS tool ?
Thank you