Your English writing platform
Discover LudwigSuggestions(2)
Exact(4)
One way to partially reduce the costs associated with multiple marker testing is a stepwise approach.
In contrast, the RT-PCR approach seems to be more sensitive and allows easy multiple marker testing [ 39, 40].
A genome-wide correction to correct for multiple marker testing was applied (Bonferroni method: p < 6.4 × 10−8 calculated from nominal p value of 0.05/total number of markers as 782,838).
Current test methods require additional serum for each marker, although alternatively methods were recently introduced that allow multiple marker testing in small volumes in the range of finger prick serum or DBS volumes.
Similar(56)
The B-allele frequencies (BAF) for each array replicate were used in a specific pipeline in R software to perform multiple marker tests after excluding the 5% of SNPs showing the highest BAF variability from the replicate arrays within tail, as well as the monomorphic SNPs.
This suggests that the use of tests such as maternal serum α-fetoprotein, alkaline phosphatase, and granulocyte colony-stimulating factor as a group or adding their results to fetal fibronectin test and cervical length test results may enhance our ability to predict spontaneous preterm birth and that the development of a multiple-marker test for spontaneous preterm birth is feasible.
Recent multiple-marker tests for risk of preterm birth show promise but continue to have limited predictive power for non-labouring women [ 34].
In association studies, multiple testing needs to be considered when multiple markers are tested independently on a phenotype [31], [32].
Maternal serum screen (also called quad screen, triple screen or test, multiple marker screen or AFP) – This is a screening test done at 15 to 20 weeks to detect a higher risk of chromosomal disorders such as Down syndrome and trisomy18 and neural tube defects such as spina bifida.
However, we suggest a multiple phospho-marker test including p-Akt-s473, p-mTOR-s2448, and p-ER-s167/s305.
Multiple markers should be tested for each chromosome of interest.
Write better and faster with AI suggestions while staying true to your unique style.
Since I tried Ludwig back in 2017, I have been constantly using it in both editing and translation. Ever since, I suggest it to my translators at ProSciEditing.

Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com