Cryptococcus neoformans (Cn) is a basidiomycete fungus that causes cryptococcosis worldwide in immunodeficiency and healthy individuals. In this pathogen, the elaboration of virulence factors including melanin and the capsule depends on intact intracellular trafficking, an essential cellular process also required for nutrient uptake, ion homeostasis, and receptor recycling.
I wonder if anyone can give me some advice on a potential pipeline for analysis of differential transcript-level expression and novel isoform discovery. The pilot project I am working on involves analysis of mRNA-seq data derived from a human cell line which has been transfected with various plasmids. Consequently we are interested not only in.
The human brain is one of the last frontiers of biome dical research. Genome -wide association studies (GWAS) have succeeded in identifying thousands of haplotype blocks associated with a range of neuropsychiatric traits, including disorders such as schizophrenia, Alzheimer s and Parkinson s disease.
QuantSeq-Flex Targeted RNA-Seq Lib. Prep Kit. SLAMseq Metabolic RNA Labeling Kit. TeloPrime Full-Length cDNA Amplification Kit V2. SPLIT RNA Extraction Kit. SIRVs (Spike-in RNA Variant Control Mixes) Mix 2 RNA-Seq Data Analysis Software. RiboCop rRNA Depletion Kit. Poly(A) RNA Selection Kit. Modules and Add-ons. SUPPORT TOOLS: Index Balance.
Analysis example for RNA-Seq experiments using the bioconductor package edgeR Analysis example for RNA-Seq experiments using the bioconductor package edgeR - Overview This is a script that will do differential gene expression (DGE) analysis for RNA-seq experiments using the bioconductor package edgeR. Project Details To give background on this.
Introduction. The swift spread of RNA technologies in recent years, mainly RNA sequencing (RNA-seq) 1-4 and associated bioinformatics 3, 5, has led to identification of a huge number of “chimeric RNAs”, or RNA chimeras, which are those RNA molecules containing sequences from two different genes.For instance, a report from the ENCODE project in 2007 estimates that transcripts from 65%, i.e.
Single-cell RNA-seq techniques have been transformative (19,20) and continue to advance RNA-based biological research, but mRNA levels alone are insufficient for characterizing, understanding, and controlling biological systems. Even at the superficial descriptive level, single-cell RNA-seq cannot capture post-translational modifications (PTMs).
Histomorphometrical essay was used to quantitatively and qualitatively assess the effects of BPA on pharyngeal cartilage development. RNA sequencing (RNA-seq) was used to discover differentially expressed genes (DEGs), and KEGG pathway and GO enrichment analysis were performed to interpret functional ontology.
Arctic charr have a circumpolar distribution, persevere under extreme environmental conditions, and reach ages unknown to most other salmonids. The Salvelinus genus is primarily composed of species with genomes that are structured more like the ancestral salmonid genome than most Oncorhynchus and Salmo species of sister genera. It is thought that this aspect of the genome may be important for.
In this essay, we redefine “two neighboring genes” as those producing individual transcripts, and point out two known mechanisms for chimeric RNA formation, i.e. transcription from a fusion gene or trans-splicing of two RNAs. By our definition, most putative RNA chimeras derived from canonically-defined neighboring genes may either be technical artifacts or be cis-splicing products of 5.
Summary: High-throughput RNA sequencing (RNA-seq) is rapidly emerging as a major quant. transcriptome profiling platform. Here, we present DEGseq, an R package to identify differentially expressed genes or isoforms for RNA-seq data from different samples. In this package, we integrated three existing methods, and introduced two novel methods.
In this study, we explored transcriptional complexity in human neutrophils, cells generally regarded as nonspecific in their functions and responses. We studied distinct human disease phenotypes and found that, at the gene, gene isoform, and miRNA level, neutrophils exhibit considerable specificity in their transcriptomes. These findings were particularly striking for isoform usage. Thus, even.
RNA polymerase II (RNAP II and Pol II) is a multiprotein complex that transcribes DNA into precursors of messenger RNA (mRNA) and most small nuclear RNA (snRNA) and microRNA. It is one of the three RNAP enzymes found in the nucleus of eukaryotic cells. A 550 kDa complex of 12 subunits, RNAP II is the most studied type of RNA polymerase.A wide range of transcription factors are required for it.