Hi, it sounds like you have not enabled the consensus option, and thus
created a raw library. See:



http://tools.proteomecenter.org/wiki/index.php?title=Software:SpectraST#Creating_Consensus_Libraries



Regards,

Eric





*From:* [email protected] [mailto:
[email protected]] *On Behalf Of *S.K.V. Adhin
*Sent:* Monday, June 10, 2013 2:10 AM
*To:* [email protected]
*Subject:* [spctools-discuss] Removing redundant spectra



Recently I made a large spectral library made 30 raw files from the
Q-Exactive.
After the mzXML conversion with msconvert I did a database search with
X!Tandem (using TPP) and retrieved 30 pep.xml files.
Subsequently I merged the 30 files with Peptideprophet into one
interact.pep.xml file.This file I used to build a spectral library with
SpectraST (also using the TPP).
This resulted in a huge spectral library with a filesize of 5GB. I was
wondering why this was such a huge file so I inspected the file with
spectral library viewer in Skyline.
I noticed that there many duplicate entries in the spectral library. I know
that one peptide can be assigned to different spectra so peptides in the
library does not have to be unique. But I found out that the spectral
library contained the same peptide assigned to the same spectra multiple
(between 10 and 25) times.
Is there a particular reason why the spectral library have so many exactly
the same entries and is there a possibility to remove them, so that at
least every spectra in the library is unique?

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