Exact(4)
Genomic regions in NRF where map length based on historic recombination was greater than map length based on recent recombination coincided with some well known QTL regions for milk production traits.
For well known quantitative trait loci (QTLs) for milk production traits on Bos Taurus chromosomes 1, 6 and 20, map length based on historic recombination was greater than map length based on recent recombination in NRF.
For well known QTL regions for milk production on BTA1, BTA6 and BTA20, map length based on historic recombination was greater than map length based on recent recombination in NRF.
The use of intravenous epinephrine was protocol driven to avoid circulatory collapse and death if MPAP was equal to or greater than MAP during the first 60 minutes [ 18].
Similar(56)
White contours indicate areas with odds significantly less than the map average (p-value < 0.10), while black contours indicate areas with odds significantly greater than the map average, that is, high-risk areas.
Areas that generate statistically significant RR scores greater than one map the geographic locations where poor (or conversely, good) patient outcomes have clustered whereas areas that generate statistically significant RR scores less than one map those areas where there is a decreased risk of either a good or poor outcome.
Although quantifying the power is complicated by the arbitrary parameterization of the background level of mapping reads, we found that under most realistic assumptions, an expected number of reads greater than 30 mapping to an exon in the test sample was sufficient to identify a homozygous deletion in either of the two datasets.
Although the estimated coverage of the chromosome arm by FPC-constructed map was greater than LTC-constructed map (78%% versus 68%%), the number of contigs in LTC-constructed map was considerably less than that of FPC, while the N50 contig size was almost twice as large (Table 1).
On average 92 % of reads aligned to the reference genome for each library, with greater than 70%% mapping uniquely (Additional file 1: Table S2).
Candidate variants in each strain were pre-filtered (depth greater than 3, mapping quality greater than 20, SNP quality greater than 20, 'heterozygous' calls excluded) to remove misalignments, then putative variants common to all four resequenced strains, representing real differences between DdB and the reference sequence, were excluded.
The marker saturation of this integrated map is far greater than previously published maps (Table 1), increasing dramatically the number of easily transferable markers from 200 [ 17] to 3353 SNPs and from 386 [ 18] to 640 SSRs.
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