DNase FAIRE data:
Filename | Description | Feature | GEO-ID | |
1 | GSE66185_all.sga | IDC|MNase|all samples | MNase | - |
2 | GSE66185_147bp_all.sga | IDC|MNase|all samples 147bp fragments | MNase | - |
3 | GSE66185_oriented_all.sga | IDC|MNase|all samples oriented | MNase | - |
4 | GSM1616484.sga | IDC|MNase|5h | MNase | GSM1616484 |
5 | GSM1616485.sga | IDC|MNase|10h | MNase | GSM1616485 |
6 | GSM1616486.sga | IDC|MNase|15h | MNase | GSM1616486 |
7 | GSM1616487.sga | IDC|MNase|20h | MNase | GSM1616487 |
8 | GSM1616488.sga | IDC|MNase|25h | MNase | GSM1616488 |
9 | GSM1616489.sga | IDC|MNase|30h | MNase | GSM1616489 |
10 | GSM1616490.sga | IDC|MNase|35h | MNase | GSM1616490 |
11 | GSM1616491.sga | IDC|MNase|40h|rep1 | MNase | GSM1616491 |
12 | GSM1616492.sga | IDC|MNase|40h|rep2 | MNase | GSM1616492 |
FASTQ files were extracted from SRA files using fastq-dump (SRA toolkit v2.5.0) and mapped to the genome using Bowtie v1.1.1. SAM files were then converted into BAM using samtools v0.1.14 and to bed using bamToBed v2.27.0 (bedtools). SGA conversion was carried out using in-house software.