ChIP-seq data:
Filename | Description | Feature | GEO-ID | |
1 | GSM1463320_NFAT1.sga | D1 dendritic cells|NFAT1|curdlan | NFAT1 | GSM1463320 |
2 | GSM1463321_Input.sga | D1 dendritic cells|Input|curdlan | Input | GSM1463321 |
3 | GSM1463322_H3K4me3.sga | D1 dendritic cells|H3K4me3|none | H3K4me3 | GSM1463322 |
4 | GSM1463323_Input.sga | D1 dendritic cells|Input|none | Input | GSM1463323 |
5 | GSM1463324_H3K4me3.sga | D1 dendritic cells|H3K4me3|curdlan2h | H3K4me3 | GSM1463324 |
6 | GSM1463325_Input.sga | D1 dendritic cells|Input|curdlan | Input | GSM1463325 |
7 | GSM1463326_H3K4me3.sga | D1 dendritic cells|H3K4me3|curdlan2h+Fk506 | H3K4me3 | GSM1463326 |
8 | GSM1463327_Input.sga | D1 dendritic cells|Input|curdlan+Fk506 | Input | GSM1463327 |
ChIP-seq peaks files:
Filename | Description | Feature | GEO-ID | |
1 | GSM1463320_NFAT1_peaks.sga | D1 dendritic cells|NFAT1 peaks|curdlan | NFAT1_P | GSM1463320 |
D1 cells were cultured and treated with or without the dectin-1 ligand curdlan and with or without the NFAT1 inhibitor Fk506.
The curdlan treated cells were rested 2 hours for H3K4me3 samples and 30 minutes otherwise
(sample treatment is 30 minutes if nothing is specified in the sample description below). FK506 treatment was 2 hours.
Samples which were not treated at all bear 'none', in their descriptions.
FASTQ files were extracted from SRA files using fastq-dump (SRA toolkit v2.5.0) and mapped to the mm9 genome using Bowtie v0.12.8. SAM files were then converted into bam using samtools v0.1.14 and to bed using bamToBed v2.12.0 (bedtools). SGA conversion was carried out using bed2sga.pl (ChIP-Seq v. 1.5.3).