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The vertical lines indicate markers between maps.
The non bold values in Table 1a indicate markers that were within the QMVR, as defined above for the normal DNA.
Bold values indicate markers that were outside the normal QMVR and would have been recorded as unstable, even in the absence of comparison with matching normal DNA.
Columns indicate markers, SNP position in the marker, the p-value of association, the percent of phenotypic variation explained by the SNP (R2 %), and SNPs from the same tag.
For mapping of segregating loci, panels A and B indicate markers that are heterozygous in both GF and UN parents, panels C and D show markers heterozygous in only the GF parent, and panels E and F markers heterozygous in only the Undine parent.
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The numbers under the marker name indicate marker's position (Mb).
The red, blue, and green symbols indicate marker tephras from Aoki and Machida (2006) and Nakamura (2016).
Completely red colonies indicate marker loss before plating and were excluded.
Columns indicate marker name, EST or Contig information in the CGPDB database, forward and reverse primers, annealing temperature (Ta), magnesium concentration in PCR reaction, and size of amplicon.
Marker colour intensity represents depth in 3D space (transparency indicates markers that are further away).
Crude analyses indicated markers for those patients with relevant levels of neck pain.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com