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Open image in new window Fig. 4 Remaining oil distribution of different linkage status in the vicinity of faults from oil production data.
The first is the different sites of remaining oil owing to the configuration of faults and formation occurrence (Qi 2004), fault combination pattern, fault linkage status (hard linkage, soft linkage, cross linkage, superimposed deformation, etc).
Fault zone features primarily refer to the occurrence, combinations, linkage status, and associated micro-amplitude structural features (Fu et al. 2011) of fault zones, which affect fault edge injection recovery relationships and thereby control remaining oil distribution.
Pairs with linkage status that could not be determined definitively received indeterminate classifications.
If at least two adjudicators concordantly assigned linkage status, the pair was tentatively classified by that assignment.
Adjudicators were unable to determine the linkage status of 3 pairs, described below, in which sequencing was completed (Supplementary Table S1).
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Haploview was also used to examine the linkage disequilibrium status amongst all SNPs, by the two pairwise LD statistics, D' and the correlation coefficient (r2), as well as the haplotype association analyses.
Following data linkage, vital status at 30 days after admission was unavailable for 160 patients (0.44%), and so the final mortality models included data for 36 037 patients.
These significant mutations were almost in a same region with an extremely strong linkage disequilibrium status, which may result from the insufficient recombination events in the F2 segregation population [ 36, 37].
LD and conditional analysis suggested this region were in extremely strong linkage disequilibrium status, especially for the LD block from 64.0 to 67.5 Mb that almost include half (732/1531) of the total significant loci.
The aim of the present study was to investigate the involvement of various alleles, genotypes, haplotypes and their linkage disequilibrium status of Taq1B (rs 1079597), Taq1D (rS311C498), S311C (rs1801028), H313H (rs 6275), and Taq1A (rs 1800497) polymorphisms in DRD2 receptor gene in causing schizophrenia and their relation to treatment response in a South Indian population of Kerala.
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