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Uzun et al. (2009) investigated the systematics of Citrus using SRAP markers, utilizing a diverse group of 83 taxa dominated by cultivated species and interspecific hybrids, but representing all tribes and subtribes within the Rutaceae.
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Genomic aberrations were assessed with a segmentation stringency of 10 consecutive genomic markers utilizing P < 0.001 as cut off, and a signal-to-noise ratio cut-off of 0.3 for amplifications and deletions.
Although greater success rates might have been achieved after PCR optimization for individual primer sets and a smaller proportion of microsatellite markers (e.g., [ 18]), our protocol reduced both time and resources spent identifying suitable markers by utilizing a single protocol.
Ebert and Peakall (2009) provide an excellent technical review on developing markers utilizing these resources.
Here, we established a simple and effective quantitative analysis of protein markers, utilizing data obtained through routine immunofluorescence analysis on CTCs non-selected according to EpCAM expression, thus expanding and complementing a previously established CTC identification methodology.
Further, there is a need of in silico discovery of polymorphism of these markers utilizing resequencing data of four additional genotypes namely, KWS230-DH1440, SynMono001, SynMono and SynTilling.
Multiple hepatic fibrosis markers utilizing either simple blood tests or measurements of components of the extracellular matrix (ECM) have been proposed, and some are in clinical use.
Additionally to the SNPs cited by the authors (rs4077632 and rs11139451), we chose four markers utilizing RegulomeDB functional annotations for the region 9q21.
A five-dimensional (5-D) clone pooling strategy for screening of bacterial artificial chromosome (BAC) clones with molecular markers utilizing highly-parallel Illumina GoldenGate assays and PCR facilitates high-throughput BAC clone and BAC contig anchoring on a genetic map.
We previously described a sensitive reporter for the endoderm marker Hex utilizing a reiterated IRES element to translationally amplify expression of the fluorescent protein Venus, encoded downstream of Hex in the endogenous locus (Canham et al., 2010).
It remains unclear whether markers utilized to identify normal and malignant mammary stem cells play a functional role.
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