Active enhancers are still understudied in colorectal cancers (CRC). Here the authors analyse active enhancers in CRC patients using genomics, transcriptomics, and epigenomics, identifying and validating variant super-enhancer loci as well as KLF3 as a relevant transcription factor
Integrated analysis of genomic and transcriptomic level changes holds promise for a better understan...
Colorectal cancer (CRC) is one of the most common cancers in the world and one of the main causes of...
<div><p>Genomic abnormalities leading to colorectal cancer (CRC) include somatic events causing copy...
In addition to mutations in genes, aberrant enhancer element activity at non-coding regions of the g...
Aim: We aim to identify driving genes of colorectal cancer (CRC) through multi-omics analysis. Mater...
2013-02-19Genome-wide association studies (GWAS) have provided a powerful approach to identify CRC c...
Genome-wide association studies have identified a great number of non-coding risk variants for color...
Enhancers regulate multiple genes via higher-order chromatin structures, and they further affect can...
BACKGROUND: Common single-nucleotide polymorphisms (SNPs) in ten chromosomal loci have been shown to...
Integrated analysis of genomic and transcriptomic level changes holds promise for a better understan...
[eng] Colorectal cancer (CRC) is a major health burden with large numbers of new cases worldwide and...
BACKGROUND:The evaluation of less frequent genetic variants and their effect on complex disease pose...
BACKGROUND: The evaluation of less frequent genetic variants and their effect on complex disease pos...
Colorectal cancer (CRC) is a complex disease that can be caused by a spectrum of genetic variants ra...
Genomic abnormalities leading to colorectal cancer (CRC) include somatic events causing copy number ...
Integrated analysis of genomic and transcriptomic level changes holds promise for a better understan...
Colorectal cancer (CRC) is one of the most common cancers in the world and one of the main causes of...
<div><p>Genomic abnormalities leading to colorectal cancer (CRC) include somatic events causing copy...
In addition to mutations in genes, aberrant enhancer element activity at non-coding regions of the g...
Aim: We aim to identify driving genes of colorectal cancer (CRC) through multi-omics analysis. Mater...
2013-02-19Genome-wide association studies (GWAS) have provided a powerful approach to identify CRC c...
Genome-wide association studies have identified a great number of non-coding risk variants for color...
Enhancers regulate multiple genes via higher-order chromatin structures, and they further affect can...
BACKGROUND: Common single-nucleotide polymorphisms (SNPs) in ten chromosomal loci have been shown to...
Integrated analysis of genomic and transcriptomic level changes holds promise for a better understan...
[eng] Colorectal cancer (CRC) is a major health burden with large numbers of new cases worldwide and...
BACKGROUND:The evaluation of less frequent genetic variants and their effect on complex disease pose...
BACKGROUND: The evaluation of less frequent genetic variants and their effect on complex disease pos...
Colorectal cancer (CRC) is a complex disease that can be caused by a spectrum of genetic variants ra...
Genomic abnormalities leading to colorectal cancer (CRC) include somatic events causing copy number ...
Integrated analysis of genomic and transcriptomic level changes holds promise for a better understan...
Colorectal cancer (CRC) is one of the most common cancers in the world and one of the main causes of...
<div><p>Genomic abnormalities leading to colorectal cancer (CRC) include somatic events causing copy...