Dear Brooke,

Thanks a lot for this help. I would like to use the ENCODE histone
modifications data and apply your peak calling method for my ChIP-seq data.
I therefore would like to understand well your method and wish you help me
out with some questions below:

- How did you normalize data from pooled replicates?
- Did you combine Input Control with ChIP-seq data to find peaks? If so, how
did you do that?

Thanks again for your help!

Thong

On Mon, Nov 8, 2010 at 9:36 PM, Brooke Rhead <[email protected]> wrote:

> Hi Thong,
>
> These are genome-wide data.  In general, unless an ENCODE track is listed
> under one of the "Pilot ENCODE" headers on the main Genome Browser page (
> http://genome.ucsc.edu/cgi-bin/hgTracks), it is genome-wide data.  Another
> way to double-check that any particular track you are using is genome-wide
> is to hit the "schema" link/button on the track details page or in the Table
> Browser.  If the table name starts with "wgEncode" it is genome-wide ("wg"
> stands for "whole genome").
>
> --
> Brooke Rhead
> UCSC Genome Bioinformatics Group
>
>
>
> On 11/07/10 17:25, NGUYEN Trung Thong wrote:
>
>> Dear friends,
>>
>> I am interested in histone modifications ChIP-seq data and have found two
>> sources (by Broad Institute and by Univ. Washington) available on the UCSC
>> Genome Browser. If you don't mind, could let me know whether these are
>> genome-wide data or just some parts of the human genome? I am using
>> genome-wide histone modifications data of Barski et al. (Cell 2007) and
>> hope
>> to have more data from different cell lines.
>>
>> Thanks a lot,
>>
>> Thong
>>
>>


-- 
Thong Nguyen
School of Mathematics, Statistics and Applied Mathematics
NUI Galway, Ireland
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