Closed sunta3iouxos closed 1 year ago
Hi sunta3iouxos,
you can run both DNA-mapping
and ChIP-seq
workflows with the --cutntag
flag. This will adjust mapping and peak calling settings, accordingly. Also, if you've got spikein in your samples, you might want to map to a hybrid genome (that can be generated with createIndices
) and the pass --useSpikeInForNorm
in the ChIP-seq
workflow.
We don't do any adjustments on the mapped fragment positions as is.
Best wishes,
Katarzyna
Hi Katarzyna, so no necessary adjustments for the cut&run protocol. thank you!
Hi all, How am I setting specific commands for the cut and Run in the ChIP-seq pipeline? the cut and tag is specific for the tn5 transposase that adjusts the fragments for +5/-7 (if I recall correctly) but MNAse is a bit different? Thank you