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When a new tumor marker assay is developed, precision should be evaluated across the entire reportable range of the assay.
Because no molecular marker assay is available, IC today is diagnosed by symptom assessment, physical examination, routine urine analysis, cystoscopy, and sometimes bladder biopsy.
As DArT assays are performed on highly parallel and automated platforms the cost of datapoint (a few cents per marker assay) is reduced by at least an order of magnitude compared to current, gel-based technologies.
As DArT assays are performed on highly parallel and automated platforms, the cost per datapoint (a few cents per marker assay) is reduced by at least an order of magnitude compared to current, gel-based technologies.
Similar(56)
Serum Ca-19.9 tumour marker assay was markedly increased at 500 kU/L (normal range 0 40).
A KASP marker assay was developed, and select lines with known disease reaction to BCMV were initially screened.
An allele specific GC-tail molecular marker assay was developed for the S117N Fallele allele identified in line 17D [ 34].
A SimpleProbe based molecular marker assay was developed to track the single base deletion in KK24/M25 (Additional files 3 and 4).
Based on our previous experience (Buccheri, 1999), tumour marker assay was considered an essential part of the patients' clinical evaluation and no formal informed consent was required for this study.
An allele specific molecular marker assay was developed to distinguish soybean lines with deletion of FAD2-1A (FallelesΔ alleles from M23) and the soybean lines with the presence of one (heterozygous) or two FAD2-1A alleles.
An allele specific molecular marker assay was developed for the mutation identified in line 397 to discriminate between wild-type Williams 82 or mutant alleles of the RS2 gene.
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