Hi Joe,

I only see the Win binaries.  Is the source available yet?

Brian




On Wed, Feb 19, 2014 at 4:19 PM, Joseph Slagel <
[email protected]> wrote:

> You'll find the latest release candidate (RC4) in:
>
>
> https://sourceforge.net/projects/sashimi/files/Trans-Proteomic%20Pipeline%20%28TPP%29/TPP%20v0.0%20%28Development%29/
>
> Since I don't expect any more changes this should be effectively 4.7.
>
> -Joe
>
>
>
> On Tue, Feb 18, 2014 at 10:28 PM, Robert Jones 
> <[email protected]>wrote:
>
>> Bjorn,
>>
>> Thank you so very much that was extremely helpful! I'll be well on my way
>> to finishing my analysis.
>>
>> -Robert M Jones
>>
>>
>> On Tuesday, February 18, 2014 6:45:24 AM UTC-7, Bjorn wrote:
>>>
>>> Hi,
>>> As far as I understand it, the TPP uses a mixture model-based approach
>>> to determine posterior probabilities and it then uses these probabilities
>>> to estimate the FDR. This can be done with or without the use of a decoy
>>> database. However, when using some of the more sophisticated options (like
>>> non-parametric modelling), you will need a decoy database to help the
>>> modelling algorithms pin down the negative distribution. Also, when the
>>> data is of not so excellent quality, the decoys can help make a better
>>> distinction between good and bad identifications.
>>>
>>> After the analysis with ProteinProphet, you get something like this in
>>> the ProteinProphet window:
>>>
>>> Prob Sens FPER Corr  Incorr
>>> 0.00 1.000 0.930 217 2874
>>> 0.10 1.000 0.337 217 110
>>> 0.20 1.000 0.337 217 110
>>> 0.30 0.915 0.216 198 55
>>> 0.40 0.865 0.152 187 34
>>> 0.50 0.816 0.102 177 20
>>> 0.60 0.777 0.074 168 14
>>> 0.70 0.747 0.058 162 10
>>> 0.80 0.647 0.019 140 3
>>> 0.90 0.608 0.010 132 1
>>> 0.95 0.569 0.005 123 1
>>> 0.96 0.547 0.004 119 0
>>> 0.97 0.529 0.003 115 0
>>> 0.98 0.507 0.002 110 0
>>> 0.99 0.470 0.001 102 0
>>> 1.00 0.152 0.000 33 0
>>>
>>> The FPER is your FDR, so if you decide to set it at 1%, you notice that
>>> this corresponds with a probability cut off of 0.90. Now, in your protein
>>> list, you accept all proteins with a prob. of 0.09 or higher, which is
>>> estimated to be 132 correct ones and 1 incorrect protein. Everything below
>>> is discarded.
>>>
>>> I found lots of info in the following papers (esp. the last paper).
>>> Hope this helps!
>>> Cheers,
>>> Bjorn
>>>
>>> [1] Choi, H., Fermin, D., and Nesvizhskii, A. I. Significance analysis
>>> of spectral count data in label-free shotgun proteomics. Mol. Cell.
>>> Proteomics 7, 12 (2008), 2373-2385.
>>>
>>> [2] Choi, H., Ghosh, D., and Nesvizhskii, A. I. Statistical validation
>>> of peptide identifications in large-scale proteomics using the target-decoy
>>> database search strategy and flexible mixture modeling. J. Proteome Res. 7,
>>> 1 (2008), 286-292.
>>>
>>> [3] Choi, H., and Nesvizhskii, A. I. False discovery rates and related
>>> statistical concepts in mass spectrometry-based proteomics. J. Proteome
>>> Res. 7, 1 (2008), 47-50.
>>>
>>> [4] Choi, H., and Nesvizhskii, A. I. Semisupervised model-based
>>> validation of peptide identifications in mass spectrometry-based
>>> proteomics. J. Proteome Res. 7, 1 (2008), 254-265.
>>>
>>> [5] Deutsch, E. W., Mendoza, L., Shteynberg, D., Farrah, T., Lam, H.,
>>> Tasman, N., Sun, Z., Nilsson, E., Pratt, B., Prazen, B., Eng, J. K.,
>>> Martin, D. B., Nesvizhskii, A. I., and Aebersold, R. A guided tour of the
>>> Trans-Proteomic Pipeline. Proteomics 10, 6 (2010), 1150-1159.
>>>
>>> [6] Keller, A., Nesvizhskii, A. I., Kolker, E., and Aebersold, R.
>>> Empirical statistical model to estimate the accuracy of peptide
>>> identifications made by MS/MS and database search. Anal. Chem. 74, 20
>>> (2002), 5383-5392.
>>>
>>> [7] Nesvizhskii, A. I. A survey of computational methods and error rate
>>> estimation procedures for peptide and protein identification in shotgun
>>> proteomics. J. Proteomics 73, 11 (2010), 2092-2123.
>>>
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>
>
>
> --
> Joe Slagel
> Institute for Systems Biology
> [email protected]
> (206) 732-1362
>
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