Messenger sequences near the P gene editing site from different passages. Consensus sequences are displayed above the chromatograms. Passages are indicated above consensus sequences. Dashed line denotes the G insertion site. Mutations identified from deep sequencing data are indicated with small black arrows.</p
<p>(A) Overlap between the predicted RNA editing events (red) with Darned (blue) and RADAR (green). ...
<p>(A) Summary of the nucleotide substitution types observed in each library. (B) Summary of nucleot...
<p>The arrows indicate the cleavage sites and the numbers show the frequency of clones sequenced.</p
(A) Strategy for MeV passaging. The original inoculum (p1) was passaged 14 times on Granta cells (L1...
Chromatograms of dideoxy-sequencing over the P gene editing site from viruses passaged on Raji or JV...
a<p>The numbers outside the parenthesis represent the numbers of RNA-Seq reads mapped to the positio...
<p>Graphs were from the antisense strand of the reference genome. Here in gene <i>rpoC2</i>, two out...
<p>The arrows indicate the primers' annealing positions. The dotted line shows the sequence obtained...
<p>Sequence analysis of cDNA PCR products encoding BmorCSP1 reveals nucleotide insertion, deletion a...
The development of new and easy-to-use nucleases, such as CRISPR/Cas9, made tools for gene editing w...
a<p>Strands are indicated with “+”, positive strand, and “−”, negative strand;</p>b<p>Base in the po...
APOBEC3A, CRISPR programmable RNA base editors, or other enzymes can edit RNA transcripts at specifi...
<p><b>(A)</b> Mean conservation (PhastCons) score of hyper-edited sites. Position 0 indicates the po...
To analyse the cis-requirements for RNA editing sites a newly developed in-vitro RNA editing system ...
<p>Upper sequence is obtained from patient's immortalized cells. Lower panel, the sequence obtained ...
<p>(A) Overlap between the predicted RNA editing events (red) with Darned (blue) and RADAR (green). ...
<p>(A) Summary of the nucleotide substitution types observed in each library. (B) Summary of nucleot...
<p>The arrows indicate the cleavage sites and the numbers show the frequency of clones sequenced.</p
(A) Strategy for MeV passaging. The original inoculum (p1) was passaged 14 times on Granta cells (L1...
Chromatograms of dideoxy-sequencing over the P gene editing site from viruses passaged on Raji or JV...
a<p>The numbers outside the parenthesis represent the numbers of RNA-Seq reads mapped to the positio...
<p>Graphs were from the antisense strand of the reference genome. Here in gene <i>rpoC2</i>, two out...
<p>The arrows indicate the primers' annealing positions. The dotted line shows the sequence obtained...
<p>Sequence analysis of cDNA PCR products encoding BmorCSP1 reveals nucleotide insertion, deletion a...
The development of new and easy-to-use nucleases, such as CRISPR/Cas9, made tools for gene editing w...
a<p>Strands are indicated with “+”, positive strand, and “−”, negative strand;</p>b<p>Base in the po...
APOBEC3A, CRISPR programmable RNA base editors, or other enzymes can edit RNA transcripts at specifi...
<p><b>(A)</b> Mean conservation (PhastCons) score of hyper-edited sites. Position 0 indicates the po...
To analyse the cis-requirements for RNA editing sites a newly developed in-vitro RNA editing system ...
<p>Upper sequence is obtained from patient's immortalized cells. Lower panel, the sequence obtained ...
<p>(A) Overlap between the predicted RNA editing events (red) with Darned (blue) and RADAR (green). ...
<p>(A) Summary of the nucleotide substitution types observed in each library. (B) Summary of nucleot...
<p>The arrows indicate the cleavage sites and the numbers show the frequency of clones sequenced.</p