Hello,
I have a data of snatacSeq of 15 batch of patients (5 patients per batch that are multiplexed ), I need to demultplexe them using genotypes...
8 results in 0.0022 seconds.
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Integration of ATACseq data with ChIPseq data
Hi all, I am experiencing some difficulties in the integration of ATACseq data with K27me3 ChIP data. Peaks were called with MACS2 --nomodel --extsize75... -
Just wanted to say Hi and ask a question
Dear Fellow Seqs, I am new here. It’s a pleasure to know you have my back. I hope we can have fun.
After my short intro, I was wondering... -
ATAC-seq with 2x150
Hi I'm wondering if anyone has experience of sequencing ATAC-seq libraries with HiSeq4000 2x150? Will this sequencing length cause any small fragments... -
ATAQ-Seq qPCR troubleshooting
Hello,
I am attempting to perform ATAQ-seq on human macrophages. I have performed the protocol, though have encountered an issue at the... -
ATAC-seq - cell/material loss during wash steps
Hi,
I am doing ATAC-seq on sorted lymphocytes, but I find that I always need more than the recommended 6 extra PCR cycles (11 total) to... -
Normalization, peal calling and differential analysis of ATAC-seq read counts
[content deleted - posted prematurely - I want to rephrase and make the question more clear]Last edited by anton.kratz; 07-21-2016, 01:58 AM. -
one third of maximum florescence intensity
Good day all,
My question pertains to calculating one third of maximum florescence intensity (MFI)
If the MFI is at 15 cycles then one third...
