Sentence examples for variants from all from inspiring English sources

We report a murine IgG1 mAb, JAR 41, which broadly cross-reacted with fHbp sequence variants from all variant groups.

Each insect gut community contained CODH variants from all three of these clades.

A similar observation was made in HIV-1 variants from all recipients in which the number of forward mutations was the highest in Env and Nef.

HIV-1 virus variants from all donors showed the lowest number of AA differences with the subtype B consensus in Gag and the highest number of differences in Env, confirming their respective highly conserved and variable nature.

The median number of total IPI-O variants from all of the isolates was 5, and most of those variants belong to class I, with a median number of 4. However there were obvious exceptions, with Guatemalan isolates #46 and #68 containing 17 and 14 IPI-O variants, respectively.

We developed a straightforward and simple protocol for extraction of basic proteins from the adipocytes, and using controlled proteolytic digestions of these proteins and LC/MS/MS we revealed recovery of histone variants from all subfamilies, namely H1, H2A, H2B, H3 and H4, in amounts sufficient to make up to 100 nanoLC/MS/MS analyses.

The human genome variant background was generated as control group by subtracting four types of disease-associated variant from all SNPs that appear in the dbSNP database.

In HIV-1 variants isolated from all recipients 9 22 months after the transmission event, a limited number of additional reversions had occurred, again both in- and outside predicted donor-HLA-restricted epitopes (Figure 1, right panels, white stacks).

Moreover, each of these rare variants differed from all other sequences by a single non-synonymous (amino acid altering) substitution at an otherwise invariant site.

Variants (Single nucleotide polymorphisms (SNPs) and Insertion/Deletions (In/Dels)) in coding as well as non-coding regions were then called from each alignment file using GATK [ 36], and the overlap of variants identified from all three alignment files was used for further analysis.

To build Venn Diagrams, the following filtering criteria were used: for somatic SNVs we required a minimum of 20X coverage depth with ≥5 variant reads from all tumor and normal samples, for indels we used coverage depth cutoff of 20 and variant reads of five for tumor samples.