Sentence examples for imperfect deletion from inspiring English sources

Exact(2)

The rest of the lines either contained no change or imperfect deletion (Fig.  3c; Table  1).

These alignments allowed us to confirm intron presence, perfect deletion, or imperfect deletion resulting in the removal or insertion of additional codons.

Similar(58)

Southern data corroborated with the PCR data as the UI lines that were found to contain the near-perfect deletion in PCR showed 3.5 kb band upon hybridization with GFP, and those having imperfect deletions (short/large indels) showed variable sizes, while the lines found to contain the parental locus showed the intact 2 kb band (Fig.  3f).

These two elements have been shown to correlate with each other within the HLA region of the human genome, a observation that might be attributed to repetitive insertions and deletions, imperfect segmental duplications or adjacent nucleotide changes[ 20] – all of these presumably localized processes.

The cysteine residues were shown only to have a limited impact on TapA function; in contrast, disruption of the N-terminal imperfect repeat by either deletion or replacement of amino acids 50 57 (TFDVSLQT) impaired biofilm formation, although the protein was still seen to localize on the cell surface.

Nearly all deletions involved imperfect repeat sequences similar to previous findings within neurons (Supplementary Table S2).

The imperfect nature of the genetic deletion event using this system (∼ 80%), and the fact that the timing of deletion is post-DNA replication (because the recombinase is under the control of a trophozoite-stage promoter) means that many of the schizonts will include a mixture of merozoites that are genetically null and wild type for the Pfama1 gene.

Sequence homology including both perfect and imperfect short repeats flanking the deletion regions were analyzed and correlated with clinical features and patients' age group.

Partial deletions of yellow, up to ∼3.7 kb in size, were also detected by PCR and sequence analysis, consistent with imperfect repair of Cas9-induced deletions.

About 21%% of the insertions and 27%% of the deletions consisted of imperfect repeats consisting of combinations of multiple motifs of different order.

Approximately 30% of mtDNA deletions have been shown to be flanked by imperfect repeats containing a few mismatches (class II deletions), and about 10% have no repeats at the deletion flanking regions [11].

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