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https://github.com/shengyongniu/bulk_ATAC_seq
This repo focus on bulk ATAC-seq analysis
https://github.com/shengyongniu/bulk_ATAC_seq
bulk-atac-seq
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This repo focus on bulk ATAC-seq analysis
- Host: GitHub
- URL: https://github.com/shengyongniu/bulk_ATAC_seq
- Owner: shengyongniu
- Created: 2017-11-03T11:48:49.000Z (about 7 years ago)
- Default Branch: master
- Last Pushed: 2018-09-15T02:39:45.000Z (over 6 years ago)
- Last Synced: 2024-02-12T23:46:05.368Z (10 months ago)
- Topics: bulk-atac-seq
- Language: Shell
- Size: 28.3 KB
- Stars: 2
- Watchers: 1
- Forks: 1
- Open Issues: 0
-
Metadata Files:
- Readme: README.md
Awesome Lists containing this project
- awesome-atac-analysis - A bioinformatic analysis pipeline for bulk ATAC-seq
README
# bulk_ATAC_seq
A bioinformatic analysis pipeline for bulk ATAC-seq
1. FastQC
- Files: fastqc.sh
- Description:
- This shell script help us understand the sequencing qualities of each samples and generate well-organized visualization of qualities2. Trimming
- Files: trim.sh
- Description:
- Check the fastqc result and decide how many bases to be trimmed3. Mapping
- Files: mapping.sh, mapping.qsub
- Description:
- Map reads and check reads size by the follwing script
4. Reads size check- Files: flagstat.sh
- Description:
- check the reads mapping size for experimental adjustment5. Sort and remove duplicates
- Files: sam2Sortedbam_rmdup.qub, sam2Sortedbam_rmdup.sh
- Description:
- sort reads and remove duplicates. Note: Be careful for the memory issues. Need to check the result logs and set tmp dir in argument. Also,6. Trim ChrY, ChrM, chrUn, and shift the coordinates
- Files: trim_Un_chY_chM_shift.qsub, trim_Un_chY_chM_shift.sh
- Description:
- This file help trim the unused chromosome reads and shift the coordinates for the experimental reason of ATAC-seq7. Delete negative reads
- Files: delete_negative.sh
- Description:
- Delete the reads that are shifted to negative coordination8. Convert BED file to BAM format for DiffBind
- Files: bedtobam.sh
- Description:
- This script convert the BED format to BAM format for the following DiffBind analysis9. Peaks calling
- Files: peakCalling_y.sh, peakCalling_y.qsub
- Description:
- Call peaks by DiffBind10. Filter out black list