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Potential markers were extracted from VIP plots constructed following the OPLS analysis, and markers were chosen based on their contribution to the variation and correlation within the dataset (Fig. 2d).
155 markers were extracted from 1154 markers, with at least a 20-cM interval.
Mass chromatograms and spectra were acquired with the software MassLynx (Waters) in centroid format and markers were extracted with the software MarkerLynx (Waters).
Potential markers were extracted from S-plots constructed following analysis with OPLS, and markers were chosen based on their contribution to the variation and correlation within the data set.
Therefore, given a marker position in the 50K Affymatrix genotype data, all lower and upper 2.5K SNPs around each of the 50K SNP markers were extracted from HapMap and named the 5K_HapMap dataset.
Genetic locations of the markers were extracted from the international consensus map [ 19].
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The physical positions of the markers were extract from Zea mays Genome Browser - Release 2.0.
Based on both features, internal markers are extracted by a CFAR detector and external markers are extracted by a power ratio (PR) detector.
In the first frame, markers are extracted which provide reliable seed regions for segmentation in subsequent frames.
The mapping information of SNP markers was extracted from McClean (NDSU) 2007 genetic map at Legume Information System (http://www.comparative-legumes.org/index.php/Home) [ 33].
A random sample of 25 microsatellite markers was extracted from the new microsatellite marker set and characterized on 40 accessions of melon, generating an allelic frequency database for the species.
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markers were captured
markers were calculated
markers were generated
markers were replicated
markers were recovered
traces were extracted
markers were evaluated
markers were observed
markers were investigated
markers were sorted
markers were studied
markers were designed
markers were examined
markers was extracted
markers were λ
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