Hi Kasper,
I'd like to use bsseq on a partially preprocessed whole genome
bisulfite sequencing dataset. I have a data table with one row per CpG
and columns for:
1. chromosome
2. position
3. number of reads supporting an unmethylated CpG (U)
3. number of reads supporting a methylated CpG (M)
Is it possible to turn this into an acceptable input for bsseq
(perhaps with reduced functionality), or is it essential to run the
BSmooth alignment suite to generate the complete set of columns
typically used by bsseq?
Thanks,
Martin
The information in this e-mail is intended only for the
...{{dropped:11}}
This is all you need. Look at the bsseq constructor.
Kasper
On Fri, Dec 21, 2012 at 6:40 PM, Aryee, Martin,Ph.D.
<aryee.martin at="" mgh.harvard.edu=""> wrote:
> Hi Kasper,
>
> I'd like to use bsseq on a partially preprocessed whole genome
bisulfite sequencing dataset. I have a data table with one row per CpG
and columns for:
>
> 1. chromosome
> 2. position
> 3. number of reads supporting an unmethylated CpG (U)
> 3. number of reads supporting a methylated CpG (M)
>
> Is it possible to turn this into an acceptable input for bsseq
(perhaps with reduced functionality), or is it essential to run the
BSmooth alignment suite to generate the complete set of columns
typically used by bsseq?
>
> Thanks,
> Martin
>
>
>
>
> The information in this e-mail is intended only for
th...{{dropped:8}}