<p>Exonic and intronic sequences are designated by capital and small letters, respectively. Red sequences are somatic mutations in HCCs. Blue and green numbers on the side of sequences are edit distances from splicing donor motif (AG|GTRAGT, <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0114263#pone.0114263-Zhuang1" target="_blank">[38]</a>) and splicing acceptor motif (YYYYNCAG|G), respectively. Most somatic mutations changed the edit distance to splicing donor motifs so that the corresponding alteration can be enhanced.</p
Transcript alterations often result from somatic changes in cancer genomes1. Various forms of RNA al...
Alternative splicing diversifies mRNA transcripts in human cells. This sequence-driven process can b...
Hotspot mutations in splicing factor genes have been recently reported at high frequency in hematolo...
Variations in new splicing regulatory elements are difficult to identify exclusively by sequence ins...
Background: Abnormalities of pre-mRNA splicing are increasingly recognized as an important mechanism...
Abstract Background Abnormalities of pre-mRNA splicing are increasingly recognized as an important m...
Despite a growing number of splicing mutations found in hereditary diseases, utilization of aberrant...
Substitutions that disrupt pre-mRNA splicing are a common cause of genetic disease. On average, 13.4...
Non-coding mutations can create splice sites, however the true extent of how such somatic non-coding...
<div><p>Substitutions that disrupt pre-mRNA splicing are a common cause of genetic disease. On avera...
Despite a growing number of splicing mutations found in hereditary diseases, utilization of aberrant...
<p>(A) First, we detected various types of genomic and transcriptomic changes from RNA-Seq data of 2...
Hotspot mutations in splicing factor genes have been recently reported at high frequency in hematolo...
Abstract Background An important goal of cancer genomics is to identify systematically cancer-causin...
Transcript alterations often result from somatic changes in cancer genomes1. Various forms of RNA al...
Transcript alterations often result from somatic changes in cancer genomes1. Various forms of RNA al...
Alternative splicing diversifies mRNA transcripts in human cells. This sequence-driven process can b...
Hotspot mutations in splicing factor genes have been recently reported at high frequency in hematolo...
Variations in new splicing regulatory elements are difficult to identify exclusively by sequence ins...
Background: Abnormalities of pre-mRNA splicing are increasingly recognized as an important mechanism...
Abstract Background Abnormalities of pre-mRNA splicing are increasingly recognized as an important m...
Despite a growing number of splicing mutations found in hereditary diseases, utilization of aberrant...
Substitutions that disrupt pre-mRNA splicing are a common cause of genetic disease. On average, 13.4...
Non-coding mutations can create splice sites, however the true extent of how such somatic non-coding...
<div><p>Substitutions that disrupt pre-mRNA splicing are a common cause of genetic disease. On avera...
Despite a growing number of splicing mutations found in hereditary diseases, utilization of aberrant...
<p>(A) First, we detected various types of genomic and transcriptomic changes from RNA-Seq data of 2...
Hotspot mutations in splicing factor genes have been recently reported at high frequency in hematolo...
Abstract Background An important goal of cancer genomics is to identify systematically cancer-causin...
Transcript alterations often result from somatic changes in cancer genomes1. Various forms of RNA al...
Transcript alterations often result from somatic changes in cancer genomes1. Various forms of RNA al...
Alternative splicing diversifies mRNA transcripts in human cells. This sequence-driven process can b...
Hotspot mutations in splicing factor genes have been recently reported at high frequency in hematolo...