Whole-exome sequencing (WES) and whole-genome microarray have allowed for the discovery of a wide variety of diseases that are associated with aberrations in the genome. However, these technologies may not detect some exon-level copy number variation (CNV), leaving cases unsolved. The imp...
Genomeannotation: By studying the protein content of an organism, the exact genomes responsible for the active protein compound can be determined. In this scenario results from all genomics, Transcriptomics and proteomics are important. Disease identification / Diagnostics: Proteomics is used in the ide...
Whole-exome sequencing (WES) and whole-genome microarray have allowed for the discovery of a wide variety of diseases that are associated with aberrations in the genome. However, these technologies may not detect some exon-level copy number variation (CNV), leaving cases unsolved. The ...
Whole-exome sequencing (WES) and whole-genome microarray have allowed for the discovery of a wide variety of diseases that are associated with aberrations in the genome. However, these technologies may not detect some exon-level copy number variation (CNV), leaving cases unsolved. The imp...
) and the results of the whole exome sequencing with p value <0.05. Several studies have previously proved the association between candidate genes involved in metabolic pathways of acitretin and the pathogenic mechanism of psoriasis, such as ...
Furthermore, the samples after squalene and methyl jasmonate treatment had the highest number of common transcripts (321) compared to other pairs (Figure 3). Clustering of transcripts to remove redundancy is a very sensitive step of sequence de novo assembly. Nucleotide identity between allelic ...
On average, 98.8% of these reads were mapped to the reference genome, and 83.6% were uniquely assigned to annotated exonic regions [38] (Table S1), resulting in a total of 8856 expressed genes. 3.1. Age Difference Explains more Variance than Evolutionary Responses In a PCA, the first two ...