Exact(5)
SNP UCE2-2369 was excluded from analyses because of poor genotyping on the GoldenGate platform.
One locus was censored in all analyses because of poor amplification success (<50%).
However, two samples were excluded from subsequent analyses because of poor LC/MS/MS data acquisition, leaving 22 samples for predictive model building.
This region was not included in phylogenetic analyses because of poor conservation among algal groups (for alignment see additional File 2).
Patients 4 and 7, who were sampled but excluded from the current analyses because of poor PCR performance or suspected superinfection, did not have the A*32 allele.
Similar(55)
Samples of 1 Per35/5 and 1 WT mouse were excluded from further analyses because of the poor quality of the arrays, based on the output of the Agilent feature extraction.
Although we also tried to perform similar analyses for histone H4 acetylation, we experienced difficulty with quantitative analyses because of the poor sensitivity and specificity of the anti-acetyl histone H4 antibody.
Of the 29 cattle-specific alleles, 16 were detected in 22 out of the 28 yak populations (the Nepalese yak population was excluded from admixture analyses because of their poor amplification at the majority of microsatellite loci).
The deal got postponed because of poor market conditions.
Six initially eligible patients (4%) were excluded from all subsequent analyses because of suboptimal images from poor echocardiographic windows.
Normally, a percentage of images cannot be analysed by automated methods because of poor staining.
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