Thank you so much Eric,
I will  use this....
Regards

On Fri, Dec 11, 2020, 05:06 'Eric Deutsch' via spctools-discuss <
spctools-discuss@googlegroups.com> wrote:

> Hi Sud, I think you can just use this parameter with Comet:
>
>
>
> search_enzyme_number = 0               # choose from list at end of this
> params file
>
>
>
> where 0 is defined at the bottom of the comet.params:
>
>
>
> [COMET_ENZYME_INFO]
>
> 0.  Cut_everywhere         0      -           -
>
> 1.  Trypsin                1      KR          P
>
>
>
> This tends to be a very computationally expensive search, so limiting your
> sequence database to a modest size would be beneficial.
>
>
>
> Eric
>
>
>
>
>
>
>
> *From:* spctools-discuss@googlegroups.com <
> spctools-discuss@googlegroups.com> *On Behalf Of *sudarshan kumar
> *Sent:* Thursday, December 10, 2020 2:11 AM
> *To:* spctools-discuss <spctools-discuss@googlegroups.com>
> *Subject:* [spctools-discuss] Endogenous peptide identification
>
>
>
> Dear members,
>
> I am new to this group. Can anyone help me get a standard refined search
> parameters either in comet or tandem or in any other search engine  to
> identify endogenous peptides.
>
> 1. These peptides have not been cleaved by any enzyme
>
> 2. Modification are typically not as those which happen during trypsin
> digestion.
>
> 3. Is FDR <1% in decoy search good in this case?
>
>
>
> Please reply if you have any clues.
>
> Reg,
>
> sud
>
>
>
>
>
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