COMP ID
| Parameter Description | Compound Identifier – A unique identifier assigned to each metabolite or compound in the Metabolon platform, allowing for easy reference across different datasets. |
| Protocol | The Metabolon Inc. platform used for metabolomic analysis in plasma samples. Metabolon protocol uses mass spectrometry (MS) coupled with liquid chromatography (LC-MS) to analyze a broad range of metabolites. Data was normalized to control for batch effects, and metabolites were identified using Metabolon’s proprietary library. |
BIOCHEMICAL
| Parameter Description | The metabolite – refers to the specific chemical compound identified and measured in the biological sample |
| Protocol | The Metabolon Inc. platform used for metabolomic analysis in plasma samples. Metabolon protocol uses mass spectrometry (MS) coupled with liquid chromatography (LC-MS) to analyze a broad range of metabolites. Data was normalized to control for batch effects, and metabolites were identified using Metabolon’s proprietary library. |
SUPER PATHWAY
| Parameter Description | The broader metabolic pathway category that the biochemical belongs to, such as carbohydrate, lipid or nucleotide, which encompasses a group of related biochemical processes. |
| Protocol | The Metabolon Inc. platform used for metabolomic analysis in plasma samples. Metabolon protocol uses mass spectrometry (MS) coupled with liquid chromatography (LC-MS) to analyze a broad range of metabolites. Data was normalized to control for batch effects, and metabolites were identified using Metabolon’s proprietary library. |
SUB PATHWAY
| Parameter Description | A more specific metabolic sub-pathway under the super pathway, providing finer granularity for the biochemical’s role in metabolism (e.g., glycolysis as a sub-pathway of carbohydrate metabolism) |
| Protocol | The Metabolon Inc. platform used for metabolomic analysis in plasma samples. Metabolon protocol uses mass spectrometry (MS) coupled with liquid chromatography (LC-MS) to analyze a broad range of metabolites. Data was normalized to control for batch effects, and metabolites were identified using Metabolon’s proprietary library. |
PLATFORM
| Parameter Description | The analytical technology or instrument used to measure the metabolite |
| Protocol | The Metabolon Inc. platform used for metabolomic analysis in plasma samples. Metabolon protocol uses mass spectrometry (MS) coupled with liquid chromatography (LC-MS) to analyze a broad range of metabolites. Data was normalized to control for batch effects, and metabolites were identified using Metabolon’s proprietary library. |
CHEMICAL ID
| Parameter Description | A unique identifier for the chemical compound, linked to a public database like PubChem or another chemical repository, to cross-reference compounds across platforms. |
| Protocol | The Metabolon Inc. platform used for metabolomic analysis in plasma samples. Metabolon protocol uses mass spectrometry (MS) coupled with liquid chromatography (LC-MS) to analyze a broad range of metabolites. Data was normalized to control for batch effects, and metabolites were identified using Metabolon’s proprietary library. |
RI
| Parameter Description | Retention Index is a parameter used in chromatographic analytical systems to characterize the retention behavior of a compound. It is a standardized value influenced by the chemical structure of the compound and the stationary phase in the chromatographic system. The retention index serves as an identification criterion in gas chromatography, often used in combination with mass spectrometry to provide structural information for unknown peaks |
| Protocol | The Metabolon Inc. platform used for metabolomic analysis in plasma samples. Metabolon protocol uses mass spectrometry (MS) coupled with liquid chromatography (LC-MS) to analyze a broad range of metabolites. Data was normalized to control for batch effects, and metabolites were identified using Metabolon’s proprietary library. |
MASS
| Parameter Description | The molecular mass of the chemical compound, representing the sum of the atomic masses of the atoms within the molecule. |
| Protocol | The Metabolon Inc. platform used for metabolomic analysis in plasma samples. Metabolon protocol uses mass spectrometry (MS) coupled with liquid chromatography (LC-MS) to analyze a broad range of metabolites. Data was normalized to control for batch effects, and metabolites were identified using Metabolon’s proprietary library. |
PUBCHEM
| Parameter Description | A unique accession number assigned to compounds in the PubChem database, a widely used open-source repository for chemical information. |
| Protocol | The Metabolon Inc. platform used for metabolomic analysis in plasma samples. Metabolon protocol uses mass spectrometry (MS) coupled with liquid chromatography (LC-MS) to analyze a broad range of metabolites. Data was normalized to control for batch effects, and metabolites were identified using Metabolon’s proprietary library. |
CAS
| Parameter Description | Chemical Abstracts Service (CAS) number – A unique numerical identifier assigned to each chemical substance, used to identify chemicals in databases and scientific literature. |
| Protocol | The Metabolon Inc. platform used for metabolomic analysis in plasma samples. Metabolon protocol uses mass spectrometry (MS) coupled with liquid chromatography (LC-MS) to analyze a broad range of metabolites. Data was normalized to control for batch effects, and metabolites were identified using Metabolon’s proprietary library. |
KEGG
| Parameter Description | Kyoto Encyclopedia of Genes and Genomes- is a database resource for understanding high-level functions and utilities of the biological system, such as the cell, the organism and the ecosystem, from molecular-level information, especially large-scale molecular datasets generated by genome sequencing and other high-throughput experimental technologies. |
| Protocol | The Metabolon Inc. platform used for metabolomic analysis in plasma samples. Metabolon protocol uses mass spectrometry (MS) coupled with liquid chromatography (LC-MS) to analyze a broad range of metabolites. Data was normalized to control for batch effects, and metabolites were identified using Metabolon’s proprietary library. |
HMDB
| Parameter Description | The Human Metabolome Database (HMDB) identifier – A unique accession number for metabolites in the HMDB, a comprehensive database of small molecule metabolites found in the human body. |
| Protocol | The Metabolon Inc. platform used for metabolomic analysis in plasma samples. Metabolon protocol uses mass spectrometry (MS) coupled with liquid chromatography (LC-MS) to analyze a broad range of metabolites. Data was normalized to control for batch effects, and metabolites were identified using Metabolon’s proprietary library. |
SeqId
| Parameter Description | SomaLogic sequence identifier |
| Protocol | The SOMAscan® assay by SomaLogic used for proteomic analsysis in plasma samples. |
SomaId
| Parameter Description | Target identifier, of the form SLnnnnnn (8 characters in length) |
| Protocol | The SOMAscan® assay by SomaLogic used for proteomic analsysis in plasma samples. |
TargetFullName
| Parameter Description | Target name curated for consistency with UniProt name |
| Protocol | The SOMAscan® assay by SomaLogic used for proteomic analsysis in plasma samples. |
Target
| Parameter Description | SomaLogic Target Name |
| Protocol | The SOMAscan® assay by SomaLogic used for proteomic analsysis in plasma samples. |
UniProt
| Parameter Description | UniProt identifier(s) |
| Protocol | The SOMAscan® assay by SomaLogic used for proteomic analsysis in plasma samples. |
EntrezGeneID
| Parameter Description | Entrez Gene Identifier(s) |
| Protocol | The SOMAscan® assay by SomaLogic used for proteomic analsysis in plasma samples. |
EntrezGeneSymbol
| Parameter Description | Entrez Gene Symbol names |
| Protocol | The SOMAscan® assay by SomaLogic used for proteomic analsysis in plasma samples. |
Organism
| Parameter Description | Protein Source Organism |
| Protocol | The SOMAscan® assay by SomaLogic used for proteomic analsysis in plasma samples. |
Units
| Parameter Description | Relative Fluorescence Unit |
| Protocol | The SOMAscan® assay by SomaLogic used for proteomic analsysis in plasma samples. |
Type
| Parameter Description | SOMAmer target type |
| Protocol | The SOMAscan® assay by SomaLogic used for proteomic analsysis in plasma samples. |
Protein Symbol
| Parameter Description | The abbreviated symbol representing the protein, often used as a shorthand in scientific literature to identify a particular protein. |
| Protocol | Plasma samples were screened against 1600+ antigens using the i-Ome Protein Array, followed by image analysis, data preprocessing, and quality control. Loess normalization and Combat batch correction were applied to adjust for batch effects. Further filtering included negative control filtering (NCF) and PSA (Protein Sample Antigen) filtering. |
Protein Name
| Parameter Description | The full name of the protein |
| Protocol | Plasma samples were screened against 1600+ antigens using the i-Ome Protein Array, followed by image analysis, data preprocessing, and quality control. Loess normalization and Combat batch correction were applied to adjust for batch effects. Further filtering included negative control filtering (NCF) and PSA (Protein Sample Antigen) filtering. |
Uniprot Accession
| Parameter Description | The unique identifier assigned to the protein in the UniProt database, consisting of 6 or 10 alphanumerical characters |
| Protocol | Plasma samples were screened against 1600+ antigens using the i-Ome Protein Array, followed by image analysis, data preprocessing, and quality control. Loess normalization and Combat batch correction were applied to adjust for batch effects. Further filtering included negative control filtering (NCF) and PSA (Protein Sample Antigen) filtering. |
ProteinAtlas
| Parameter Description | The Protein Atlas identifier for the protein, linking to data from the Human Protein Atlas. The format is in the Protein Atlas Identifier-Protein Symbol |
| Protocol | Plasma samples were screened against 1600+ antigens using the i-Ome Protein Array, followed by image analysis, data preprocessing, and quality control. Loess normalization and Combat batch correction were applied to adjust for batch effects. Further filtering included negative control filtering (NCF) and PSA (Protein Sample Antigen) filtering. |
Protein Class
| Parameter Description | The classification of the protein based on its biological function or molecular characteristics. |
| Protocol | Plasma samples were screened against 1600+ antigens using the i-Ome Protein Array, followed by image analysis, data preprocessing, and quality control. Loess normalization and Combat batch correction were applied to adjust for batch effects. Further filtering included negative control filtering (NCF) and PSA (Protein Sample Antigen) filtering. |
GenBank Accession
| Parameter Description | The GenBank accession number – a unique identifier assigned to the protein's genetic sequence in the GenBank database. |
| Protocol | Plasma samples were screened against 1600+ antigens using the i-Ome Protein Array, followed by image analysis, data preprocessing, and quality control. Loess normalization and Combat batch correction were applied to adjust for batch effects. Further filtering included negative control filtering (NCF) and PSA (Protein Sample Antigen) filtering. |
PPI
| Parameter Description | The protein-protein interaction of the protein, indicating whether it interacts with other proteins, which is important for understanding its role in cellular processes and pathways. |
| Protocol | Plasma samples were screened against 1600+ antigens using the i-Ome Protein Array, followed by image analysis, data preprocessing, and quality control. Loess normalization and Combat batch correction were applied to adjust for batch effects. Further filtering included negative control filtering (NCF) and PSA (Protein Sample Antigen) filtering. |
Subcellular Localisation
| Parameter Description | The location within the cell where the protein is primarily found, such as nucleus, cytoplasm, or mitochondria, which is important for understanding its function. |
| Protocol | Plasma samples were screened against 1600+ antigens using the i-Ome Protein Array, followed by image analysis, data preprocessing, and quality control. Loess normalization and Combat batch correction were applied to adjust for batch effects. Further filtering included negative control filtering (NCF) and PSA (Protein Sample Antigen) filtering. |
Transmembrane
| Parameter Description | Indicates whether the protein spans the transmembrane |
| Protocol | Plasma samples were screened against 1600+ antigens using the i-Ome Protein Array, followed by image analysis, data preprocessing, and quality control. Loess normalization and Combat batch correction were applied to adjust for batch effects. Further filtering included negative control filtering (NCF) and PSA (Protein Sample Antigen) filtering. |