Maximum likelihood inference of imprinting and allele-specific expression from EST data
Author(s) -
Cathal Seoighe,
Victoria Nembaware,
Konrad Scheffler
Publication year - 2006
Publication title -
bioinformatics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.599
H-Index - 390
eISSN - 1367-4811
pISSN - 1367-4803
DOI - 10.1093/bioinformatics/btl521
Subject(s) - genomic imprinting , biology , allele , genetics , imprinting (psychology) , gene , computational biology , single nucleotide polymorphism , dna methylation , gene expression , genotype
In a diploid organism the proportion of transcripts that are produced from the two parental alleles can differ substantially due, for example to epigenetic modification that causes complete or partial silencing of one parental allele or to cis acting polymorphisms that affect transcriptional regulation. Counts of SNP alleles derived from EST sequences have been used to identify both novel candidates for genomic imprinting as well as examples of genes with allelic differences in expression.
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