about
Evolution of genes and genomes on the Drosophila phylogenyDiRE: identifying distant regulatory elements of co-expressed genes.Homotypic clusters of transcription factor binding sites are a key component of human promoters and enhancersTissue-specific and ubiquitous expression patterns from alternative promoters of human genes.Transposable elements and their identification.Bidirectional promoters as important drivers for the emergence of species-specific transcripts.Genome-wide detection of a TFIID localization element from an initial human disease mutation.Spliceosomal small nuclear RNA genes in 11 insect genomes.Pan-cancer stratification of solid human epithelial tumors and cancer cell lines reveals commonalities and tissue-specific features of the CpG island methylator phenotypeAscertaining regions affected by GC-biased gene conversion through weak-to-strong mutational hotspots.Functional analysis of synonymous substitutions predicted to affect splicing of the CFTR gene.Do transposable elements really contribute to proteomes?The functional relevance of somatic synonymous mutations in melanoma and other cancers.Whole-genome sequencing identifies a recurrent functional synonymous mutation in melanomaA Case of IL-7R Deficiency Caused by a Novel Synonymous Mutation and Implications for Mutation Screening in SCID Diagnosis.Recurrent patterns of DNA methylation in the ZNF154, CASP8, and VHL promoters across a wide spectrum of human solid epithelial tumors and cancer cell lines.Mastering seeds for genomic size nucleotide BLAST searches.CpG island methylator phenotype in adenocarcinomas from the digestive tract: Methods, conclusions, and controversies.Significant associations between driver gene mutations and DNA methylation alterations across many cancer types.CAGI experiments: modeling sequence variant impact on gene splicing using predictions from computational toolsTransposable elements as a significant source of transcription regulating signalsTransposable Elements: Classification, Identification, and Their Use As a Tool For Comparative GenomicsAssessing predictions of the impact of variants on splicing in CAGI5
P50
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P50
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P106
P1153
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6504583035
P21
P31
P4012
P496
0000-0001-7857-3309