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| author | Bonface | 2024-02-13 23:52:26 -0600 |
|---|---|---|
| committer | Munyoki Kilyungi | 2024-08-09 13:30:43 +0300 |
| commit | b2feda451ccfbeaed02dce9088d6dd228cf15861 (patch) | |
| tree | 3dd2883524985114070a7770cd2e9f9bd7eb1848 /general/datasets/Epfl_lisp_livpmetcd1213 | |
| parent | d029d5d7f8ead1f1de8d318045004a4a6f68f5fb (diff) | |
| download | gn-docs-b2feda451ccfbeaed02dce9088d6dd228cf15861.tar.gz | |
Update dataset RTF Files.
Diffstat (limited to 'general/datasets/Epfl_lisp_livpmetcd1213')
| -rw-r--r-- | general/datasets/Epfl_lisp_livpmetcd1213/cases.rtf | 1 | ||||
| -rw-r--r-- | general/datasets/Epfl_lisp_livpmetcd1213/processing.rtf | 3 | ||||
| -rw-r--r-- | general/datasets/Epfl_lisp_livpmetcd1213/summary.rtf | 1 |
3 files changed, 5 insertions, 0 deletions
diff --git a/general/datasets/Epfl_lisp_livpmetcd1213/cases.rtf b/general/datasets/Epfl_lisp_livpmetcd1213/cases.rtf new file mode 100644 index 0000000..7d496bc --- /dev/null +++ b/general/datasets/Epfl_lisp_livpmetcd1213/cases.rtf @@ -0,0 +1 @@ +<p>For liver metabolites, livers were perfused, frozen in liquid nitrogen, and then shattered in liquid nitrogen with a mortar and pestle at a later date. Several pieces of shattered liver totalling ~100 milligrams were collected then homogenized in 1mL 70% Ethanol at -20°C. Metabolites were extracted by adding 7mL 70% Ethanol at 75°C for 2 min. Extracts were centrifuged for 10 minutes at 4,000 rpm at 4°C. Clean metabolites extracts were dried in a vacuum centrifuge and re-suspended in double-distilled H2O with volume according to the weight of the extracted liver piece. Quantification of metabolites was performed on an Agilent 6550 QTOF instrument by flow injection analysis time-of-flight mass spectrometry (see: PMID 21830798). All samples were injected in duplicates. Ions were annotated based on their accurate mass and the Human Metabolome Database reference list (see: PMID 23161693) allowing a tolerance of 0.001 Da. Unknown ions and those annotated as adducts were discarded. Theoretical m/z ratios—beyond the significant digits from the measurement sensitivity—are used as the unique index in the online data on GeneNetwork. For example, deprotonated fumarate corresponds to 115.0036897_MZ, malate to 133.0142794_MZ, α-ketoglutarate to 145.0141831_MZ, and D2HG to 147.0298102_MZ.</p>
diff --git a/general/datasets/Epfl_lisp_livpmetcd1213/processing.rtf b/general/datasets/Epfl_lisp_livpmetcd1213/processing.rtf new file mode 100644 index 0000000..671c357 --- /dev/null +++ b/general/datasets/Epfl_lisp_livpmetcd1213/processing.rtf @@ -0,0 +1,3 @@ +<p>GeneNetwork displays only the strain averages ± SEM for each metabolite. To obtain the individual data for each animal, please use the link above under (<strong>Download datasets and supplementary data files)</strong>. Note that this contains two entries for each animal: these are technical replicates. </p>
+
+<p>The <em>very</em> raw spectral data from the mass spectrometer can be downloaded on MassIVE ( <a href="http://massive.ucsd.edu/ProteoSAFe/static/massive.jsp?redirect=auth" target="_blank">http://massive.ucsd.edu/ProteoSAFe/static/massive.jsp?redirect=auth</a> ) under the identifier MSV000079411. This spectral data is for all 290 individual animals, and it includes two technical replicates for each individual, for a total of 580 runs. The file size is 102 GB and we do not recommend downloading this unless you are specifically interested in re-analyzing the spectra from scratch and looking into the granular details of mass spectrometry metabolomics.</p>
diff --git a/general/datasets/Epfl_lisp_livpmetcd1213/summary.rtf b/general/datasets/Epfl_lisp_livpmetcd1213/summary.rtf new file mode 100644 index 0000000..5f92c0e --- /dev/null +++ b/general/datasets/Epfl_lisp_livpmetcd1213/summary.rtf @@ -0,0 +1 @@ +<p>We identified 979 unique metabolite features based on mass-charge ratios (m/z) using flow-injection ToF-MS, respectively. Of these features, 699 could be attributed to a single metabolite, including in cases where of the two “possible” enantiomers, one is clearly far more predominant than the other (e.g. L versus D amino acids). The remaining 280 metabolites were “clusters” with no clear predominant feature—for example, the “glucose” metabolite measurements could not be separated from fructose, galactose, or mannose measurements, as all share the same m/z. The “main” metabolite, as well as all possible alternatives are listed with the data on <a href="http://genenetwork.org/" target="_blank">GeneNetwork.org</a> for the raw file download (press the “INFO” button next to the dataset on the main search page and download the dataset and supplemental data files).</p>
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