Databases Available for RNA-Seq Datasets
Several databases curate RNA-Seq data, which can be useful for analyzing gene expression in various biological contexts, such as cancer…
Bioinformatics, AI, Genomics, Proteomics and Transcriptomics
Several databases curate RNA-Seq data, which can be useful for analyzing gene expression in various biological contexts, such as cancer…
In RNA-Seq analysis, duplicated reads can arise from different sources, and whether to remove them is a debated issue. This…
To disable the reverse complement strand search in BLASTn, you can use the -strand option, which controls which strand of…
If you have a list of Entrez IDs and want to convert them into gene names, there are various methods…
Here’s a comprehensive guide to tools and software for phylogenetic tree visualization, focusing on large datasets. This includes recommendations for…
Parsing large FASTQ files requires memory-efficient and computationally optimized methods. Below are step-by-step instructions using various tools and programming languages…
Step-by-Step Instructions 1. Install Required Packages Ensure the following R packages are installed: R Copy code install.packages(“ggplot2”) install.packages(“ggrepel”) if (!requireNamespace(“BiocManager”,…
Introduction to Ka/Ks Ratios The Ka/Ks ratio, also known as the dN/dS ratio, is a widely used metric in molecular…
1. Introduction Venn and Euler diagrams are powerful tools for representing logical relationships among datasets. However, plotting diagrams for more…
Introduction Paired-end sequencing is widely used in next-generation sequencing (NGS) to generate reads from both ends of DNA fragments, providing…
This guide is designed to provide a detailed and structured manual for downloading all SRA (Sequence Read Archive) samples associated…
1. Introduction to Chimeric Reads Chimeric reads are sequencing reads that align to two or more distinct genomic regions, often…
Introduction Next-Generation Sequencing (NGS) has revolutionized genomic research by enabling rapid and high-throughput sequencing of DNA and RNA. Common platforms…
In the fast-paced world of bioinformatics, staying informed about the most relevant and promising research areas is crucial, especially for…
Introduction In bioinformatics and molecular biology, understanding the difference between CDS (Coding Sequence) and ORF (Open Reading Frame) is essential…
Introduction Survival analysis is a powerful statistical tool used in bioinformatics to understand the relationship between gene expression data and…
Getting Up to Speed on Unix for Bioinformatics 1. Introduction to Unix Why Learn Unix? Unix is the backbone of…
RNA sequencing (RNA-Seq) is a powerful technique for studying gene expression. To analyze RNA-Seq data, bioinformaticians use tools like STAR,…
This step-by-step manual is tailored for beginners in bioinformatics who are looking to dive into R programming. R is a…
What Are Classical Papers in Bioinformatics? Classical papers in bioinformatics are landmark studies or reviews that have profoundly shaped the…