-
Hi HiTMaP team,
Currently I have been running through your mouse brain example data. However, I encountered an error:
## Codes I used:
```
fastafile
-
Hi everyone
I am new to FlashFLQ and I try to use it to quantify my proteomics data. The identification was done with sage and MS2 Rescore. I tried to generate the generic table for FlashLFQ with the…
-
Hey,
This is not an actual issue regarding the project, but I didn't know where to ask instead. So I have a dataframe that contains m/z and intensity arrays as well as cluster labels. I want to eva…
-
Hi,
I want to analyze LFQ-DIA global proteome and phospho-enriched proteome data separately on DIA-NN. Just want to make sure that we need two different libraries for these two different searches, r…
-
Hei,
I stumbled into an issue with the RIKEN/PR3* spectra. It seems, that the exact mass is not correctly calculated. Let's look at the following example:
[PR302491.txt](/MassBank/MassBank-data…
-
Hi Johannes,
I finally had another look on the package with some first data. Unfortunately, the precursor mass is NA for MS2 spectra...
´´´
ftest
chufz updated
6 months ago
-
The current mass spectra is just for a single scan i.e one retention time. It may be helpful if the mass spectra can be plotted for a rt range.
UI: Mass spectra can be updated by selecting some re…
-
These lines in `clusters.py` cause quite some warnings that the file `V` cannot be found:
https://github.com/AstarVienna/ScopeSim_Templates/blob/dc42d529bd88009d73d37477a39d950112a4b4f5/scopesim_te…
-
We should check if we can export data to a file and import it again without larger losses.
Currently, of I export spectra to `mgf` files and load them again, `parent_mass` entries will become a strin…
-
Article title: "Primeval very low-mass stars and brown dwarfs – III. The halo transitional brown dwarfs"
https://academic.oup.com/mnras/article/479/1/1383/5001885
the supplementary data on the w…