<p>A) Read pileup of the superset reads showing coverage in exons and specific introns. Canonical HTT gene model is in blue. B) Relative contribution of reads from each disease dataset to the superset binned into exon (top) and intron (bottom) features. Each bar is the average number of covered bases per base position in the given feature divided by the number of samples in the corresponding condition. The canonical gene model lies between the bar charts. High intronic coverage is apparent in introns 9, 10, 12, 41, 49, and 58, highlighted in grey. None of the features are obviously biased toward any of the conditions. The rightward skew of counts is indicative of the poly-A selection method used in library prep.</p
The spliceosome catalyzes the removal of introns from pre-messenger RNA (mRNA) and subsequent pairin...
Background: In Huntington's disease (HD), a CAG repeat expansion mutation in the Huntingtin (HTT) ge...
Background: Alternative polyadenylation sites within a gene can lead to alternative transcript varia...
<div><p>Despite 20 years since its discovery, the gene responsible for Huntington’s Disease, <i>HTT<...
Despite 20 years since its discovery, the gene responsible for Huntington's Disease, HTT, has still ...
Despite 20 years since its discovery, the gene responsible for Huntington’s Disease, HTT, has still ...
Background HD pathogenic mechanisms are complex with studies largely centred on the mutant HTT prote...
Post-transcriptional regulation is a set of important biological functions taking place during the g...
<p>Grey areas indicate overall aligned read coverage in the region, black areas are the spliced read...
Background: A CAG repeat expansion in HTT has been known to cause Huntington’s disease for over 20 y...
In this issue of Neuron, Johnson et al. employ a unique whole-genome exon-level analysis of the deve...
A) The bar graph reports the number of differential AS events in the NPC and ESC from KI models of H...
A) Bar graphs show the number of differential AS events in the striatum and cortex from 6 mouse KI m...
We construct and analyse a computational model that predicts the outcome of alternative splicing by ...
A key parameter in the experimental design of poly(A) RNA-seq projects is the choice of sequencing d...
The spliceosome catalyzes the removal of introns from pre-messenger RNA (mRNA) and subsequent pairin...
Background: In Huntington's disease (HD), a CAG repeat expansion mutation in the Huntingtin (HTT) ge...
Background: Alternative polyadenylation sites within a gene can lead to alternative transcript varia...
<div><p>Despite 20 years since its discovery, the gene responsible for Huntington’s Disease, <i>HTT<...
Despite 20 years since its discovery, the gene responsible for Huntington's Disease, HTT, has still ...
Despite 20 years since its discovery, the gene responsible for Huntington’s Disease, HTT, has still ...
Background HD pathogenic mechanisms are complex with studies largely centred on the mutant HTT prote...
Post-transcriptional regulation is a set of important biological functions taking place during the g...
<p>Grey areas indicate overall aligned read coverage in the region, black areas are the spliced read...
Background: A CAG repeat expansion in HTT has been known to cause Huntington’s disease for over 20 y...
In this issue of Neuron, Johnson et al. employ a unique whole-genome exon-level analysis of the deve...
A) The bar graph reports the number of differential AS events in the NPC and ESC from KI models of H...
A) Bar graphs show the number of differential AS events in the striatum and cortex from 6 mouse KI m...
We construct and analyse a computational model that predicts the outcome of alternative splicing by ...
A key parameter in the experimental design of poly(A) RNA-seq projects is the choice of sequencing d...
The spliceosome catalyzes the removal of introns from pre-messenger RNA (mRNA) and subsequent pairin...
Background: In Huntington's disease (HD), a CAG repeat expansion mutation in the Huntingtin (HTT) ge...
Background: Alternative polyadenylation sites within a gene can lead to alternative transcript varia...