To your question if that data is already in prDB - decryptM: YES it is ! e.g.
www.proteomicsdb.org/drug/107070/...
also i can recommend the interactive dashboards.html on zenodo to explore the data locally
zenodo.org/records/1609...
To your question if that data is already in prDB - decryptM: YES it is ! e.g.
www.proteomicsdb.org/drug/107070/...
also i can recommend the interactive dashboards.html on zenodo to explore the data locally
zenodo.org/records/1609...
Let me know if you need some tricks for the time-dependent hack and good luck with the paper
Let me know if you need some tricks for the time-dependent hack and good luck with the paper
3/3
3/3
We are running the astral mostly without FAIMS and experienced for us normal exploris-like cleaning cycles.
We are running the astral mostly without FAIMS and experienced for us normal exploris-like cleaning cycles.
there are exactly 222 active and alumni members in the folder structure. Wow quite a crowd by now :)
there are exactly 222 active and alumni members in the folder structure. Wow quite a crowd by now :)
In Europe, you pay ~ 8k for a TMT 16 plex (the 5 mg bag). This means: ~8k Eur / 50 batches / 16 samples = ~10 Eur / sample. If they could allow 5 to 2 Eur, that would be game changing.
In Europe, you pay ~ 8k for a TMT 16 plex (the 5 mg bag). This means: ~8k Eur / 50 batches / 16 samples = ~10 Eur / sample. If they could allow 5 to 2 Eur, that would be game changing.
This iTRAQ to TMT mass range should be fine and only C/N encoding. I just don't know how stable this free double bond is in the gas phase. The others always used a ring. But it's the same for all TMT channels, so maybe fine anyway.
This iTRAQ to TMT mass range should be fine and only C/N encoding. I just don't know how stable this free double bond is in the gas phase. The others always used a ring. But it's the same for all TMT channels, so maybe fine anyway.
But there are many small challenges to solve: bigger tags, which resolutions is needed, thermo would need to open the MS e.g custom phiSDM masses, how clean is the mz area…
But there are many small challenges to solve: bigger tags, which resolutions is needed, thermo would need to open the MS e.g custom phiSDM masses, how clean is the mz area…
- potency -> which target caused the effect? Does it meet my expectation?
- effect size -> what is the biological response strength to the perturbation?
- direction -> is it inhibitory or activating?
- significance -> can I trust this observation?
- potency -> which target caused the effect? Does it meet my expectation?
- effect size -> what is the biological response strength to the perturbation?
- direction -> is it inhibitory or activating?
- significance -> can I trust this observation?