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For SIs and NPCIs, a pattern of decreasing spread among coverage probabilities for QTL in all marker densities is visible across sub-simulations with the QTL not on the left marker (10 50% distance).
Significant segregation distortion was found in all marker types and on all linkage maps constructed (Table 1).
We find that significant amounts of the genetic variance in all marker systems are explained by among-population structures.
Within the Maldives, we find a subtle genetic substructure in all marker systems that is not directly related to geographic distance or linguistic dialect.
Both clustering of markers and segregation distortion (which has been identified in hop previously [ 15, 16]) was not limited to one marker type, but was evident in all marker types used, suggesting that they are not artefacts of genotyping error.
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Finally, 21 plants with all the three qDTY specific alleles in all the marker loci and the recipient parent at the QTL flanking loci were identified.
In all these markers the ratio was skewed toward a higher frequency of the paternal allele.
Despite the low level of spatial assimilation, defectors showed progress in other markers of assimilation, and those that desired to move out of housing showed higher levels of assimilation in all markers.
This strain is indistinguishable from WA MRSA-55/56 in all markers covered by the microarray with the sole exception of the SCCmec element.
A cluster of syntenic FI-markers displays a chromosome-specific pattern of F2 genotypes, which is identical for all loci on the same chromosome and which displays the exact opposite pattern in all markers in repulsion.
There were no significant alterations in protein levels of glutamate decarboxylase (GAD) 65/67, NMDA receptor1 (NR1), and NMDA receptor 2A/2B (NR2A/2B) in the fontal cortex (Fig. 6A) as well as in all markers examined in other brain regions (Fig. 6B, C).
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com