A novel method for identification and quantification of consistently differentially methylated regions.
Texto
Documentos relacionados
RNA-Seq was performed on the same RNA pools used to quantify hypoxic enhancer activity in order to identify putative target genes proximal to identified enhancer
The Cancer Genome Ana- tomy Project has created a SAGE database of human gene expression levels for many different tumors and normal reference tissues and provides online tools
Methodology and Findings: We analyzed the genome-wide patterns of gene expression with DNA microarrays in skin biopsies from distinct scleroderma subsets including 17 patients
Methods: The genome-wide gene expression profiling were conducted in 10 pairs of cancer tissues and corresponding normal adjacent tissues samples using Affymetrix GeneChip H
In this study, we performed a genome-wide identification and characterisation of invertase genes from Populus and revealed an invertase gene family with a total of 24 members
To profile differentially expressed lncRNAs in hepatoblastoma, we performed a genome-wide analysis of lncRNA and mRNA expression in hepatoblastoma and matched normal tissues
Expression patterns of both cork oak genes, QsSHR1 and QsSHR2 , in different tissues were examined and a comparative analysis of SHR transcript levels in
Pseudoplatystoma corruscans , Pseudoplatystoma reticulatum and hybrid ‘Surubim’ were detected using multiplex PCR and PCR-RFLP in RAG2, GLOBIN, EF1 α , 18S rRNA nuclear genes,