The phrase "assay database" is correct and usable in written English.
It can be used in contexts related to scientific research, particularly in fields like chemistry or biology, where assays are conducted and data is stored.
Example: "The researchers accessed the assay database to analyze the results of their experiments."
Alternatives: "test results database" or "analysis data repository".
The analysis is focused on evaluating the code performance in predicting isotopic compositions in spent nuclear fuel by using an extensive, measured isotopic assay database.
We apply this technique to a large assay database (>90,000 samples) from the Kevitsa Nickel-Copper-Platinum group element (PGE) deposit in Finland.
The flowchart for the script is outlined in Fig. 10, which involves both 'ESearch' (to query the gene and protein databases) and 'ELink' (to connect to the assay database) procedures to obtain all Gene IDs (GIDs) and Protein IDs (PIDs) for a given UniProt Accession (including any IDs that are not included in UniProt) [56].
Primer sequences are available at the PyroMark Assay Database (Biotage, Sweden) for all assays with the exception of p16INK4A, and were designed to hybridize with CpG-free regions to secure methylation-independent amplification.
aAssay ID: numbers are from the validated assay database at ABI aPreviously designed sequence reported in [ 30].
The MMP1 SNP (rs1799750) was analysed with a pyrosequencing-method based on an assay from PyroMark Assay Database (Qiagen).
The detailed conditions for LC-MS/MS and in vitro kinase activity assay, and database search parameters are described in the online Supporting Information.
The detailed target annotations in the PubChem BioAssay database (assay identifier: AID) made this step very straightforward.
The training sets for the benchmarked models were obtained from PubChem BioAssay database (assays AID410, AID883, AID899, AID884 and AID891 for CYP1A2, 2C9, 2C19, 3A4 and 2D6, respectively).
This sparse connectivity pattern in A is defined by ZA, which can be obtained from ChIP-chip assay or existing databases.
Of CNVs >10 kb, a high proportion is tagged by PRT assays in the database; smaller CNVs are less likely to contain a pre-designed PR.
