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> samples
SampleID Tissue Factor Condition Treatment Replicate
1 BT4741 BT474 ER Resistant Full-Media 1
2 BT4742 BT474 ER Resistant Full-Media 2
3 MCF71 MCF7 ER Responsive Full-Media 1
4 MCF72 MCF7 ER Responsive Full-Media 2
5 MCF73 MCF7 ER Responsive Full-Media 3
6 T47D1 T47D ER Responsive Full-Media 1
7 T47D2 T47D ER Responsive Full-Media 2
8 MCF7r1 MCF7 ER Resistant Full-Media 1
9 MCF7r2 MCF7 ER Resistant Full-Media 2
10 ZR751 ZR75 ER Responsive Full-Media 1
11 ZR752 ZR75 ER Responsive Full-Media 2
bamReads ControlID bamControl
1 reads/Chr18_BT474_ER_1.bam BT474c reads/Chr18_BT474_input.bam
2 reads/Chr18_BT474_ER_2.bam BT474c reads/Chr18_BT474_input.bam
3 reads/Chr18_MCF7_ER_1.bam MCF7c reads/Chr18_MCF7_input.bam
4 reads/Chr18_MCF7_ER_2.bam MCF7c reads/Chr18_MCF7_input.bam
5 reads/Chr18_MCF7_ER_3.bam MCF7c reads/Chr18_MCF7_input.bam
6 reads/Chr18_T47D_ER_1.bam T47Dc reads/Chr18_T47D_input.bam
7 reads/Chr18_T47D_ER_2.bam T47Dc reads/Chr18_T47D_input.bam
8 reads/Chr18_TAMR_ER_1.bam TAMRc reads/Chr18_TAMR_input.bam
9 reads/Chr18_TAMR_ER_2.bam TAMRc reads/Chr18_TAMR_input.bam
10 reads/Chr18_ZR75_ER_1.bam ZR75c reads/Chr18_ZR75_input.bam
11 reads/Chr18_ZR75_ER_2.bam ZR75c reads/Chr18_ZR75_input.bam
Peaks PeakCaller
1 peaks/BT474_ER_1.bed.gz bed
2 peaks/BT474_ER_2.bed.gz bed
3 peaks/MCF7_ER_1.bed.gz bed
4 peaks/MCF7_ER_2.bed.gz bed
5 peaks/MCF7_ER_3.bed.gz bed
6 peaks/T47D_ER_1.bed.gz bed
7 peaks/T47D_ER_2.bed.gz bed
8 peaks/TAMR_ER_1.bed.gz bed
9 peaks/TAMR_ER_2.bed.gz bed
10 peaks/ZR75_ER_1.bed.gz bed
11 peaks/ZR75_ER_2.bed.gz bed
but, as far as I understand (Am i wrong ?) the peak calling is only generated for the merged data, so i would be nice to have an option to generate the peaks for each replicate. (Unless there is a cool nf-project that is able to find the differential peaks between two ATACSeq conditions, but I have not found it )
The text was updated successfully, but these errors were encountered:
We had ambitions in this regard, but it hasn't been optimised for it yet, so I'd say it's unsupported right now and I don't know if it's an appropriate solution.
The peaks generated for each replicate can be found under <ALIGNER>/merged_library/macs2/<PEAK_TYPE>, see the example of the full test here. Likewise, the bam files can be found in <ALIGNER>/merged_library/, see again the example here. Hope this helps.
Description of feature
Hi all, I've been asked to run diffbind on our ATACseq data; Unless I'm wrong diffbind requires a samplesheet with each replicate and, for each replicate a BAM and a peaks/bed: https://bioconductor.org/packages/release/bioc/vignettes/DiffBind/inst/doc/DiffBind.pdf
but, as far as I understand (Am i wrong ?) the peak calling is only generated for the merged data, so i would be nice to have an option to generate the peaks for each replicate. (Unless there is a cool nf-project that is able to find the differential peaks between two ATACSeq conditions, but I have not found it )
The text was updated successfully, but these errors were encountered: