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Using a dataset of highly common markers makes it possible to increase the confidence interval of a QTL.
Lack of individual HR data of other markers makes it difficult to exclude the influences by confounding factors in a meta-analysis.
Unfortunately, the lack of simple markers makes it hard to detect CSCs in situ and find out their adjacent cells providing Notch ligands by current immunostaining techniques.
Nevertheless, the presence of SSR markers in these groups together with the RFLP markers makes it more convenient for genetic map integration or comparison.
Co-expression of any of these markers makes it difficult to isolate a sufficient amount of pure CSC populations for drug screening.
Use of these size markers makes it easy to determine if the unknown is within the expected size range of that species.
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Increased teacher workloads and the reluctance of headteachers to encourage their staff to act as markers made it harder for the boards to recruit.
Advances in the use of stable isotope markers make it possible to track a diversity of animal species in a variety of habitats.
Additionally, the presence of many unassigned chromosomal fragments (markers) made it difficult to determine the true level of aneuploidy.
Together these markers made it possible to distinguish between PROS expression in NBs, GMCs and GCs (prospective neurons) (see Table 1).
Individual steps in blood cell differentiation are well defined by specific markers, making it an ideal system to determine the relationship between nestin/GR colocalization and the status of cell differentiation.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com