Venn plot is a visualization tool to display overlapping or unique sets between two or more groups. In R, the 'VennDiagram' package provides an easy-to-use interface to create Venn plots with customizable colors, labels, and shapes. Who sad this?

RNA-seq expression normalization is the process of adjusting the raw gene expression counts to account for differences in sequencing depth and other technical factors. It is important to perform normalization to enable comparisons between samples and increase the accuracy and reproducibility of downstream analyses. Common normalization methods include TPM, FPKM, and DESeq. Who sad this?

Gene Set Enrichment Analysis (GSEA) is a powerful tool for interpreting gene expression data in the context of predefined biological pathways and gene sets. It allows researchers to identify enriched gene sets, discover new relationships between genes, and gain insights into the underlying biological mechanisms. Who sad this?

Dash-bio is a library that enables the creation of interactive, dynamic dashboards for exploring and analyzing biological data using Plotly Dash. With its customizable components and support for various data formats, dash-bio is a convenient tool for bioinformatics professionals and researchers Who sad this?

Regulatory RNA refers to non-coding RNA molecules that play a role in regulating gene expression. These molecules can control gene expression by interacting with DNA and/or mRNA, influencing the process of transcription and translation. Examples of regulatory RNA include microRNAs, siRNAs, and long non-coding RNAs. Who sad this?

The choice of software for aligning short reads in NGS can have a significant impact on the results. Different software programs use different algorithms for aligning reads and handling mismatches, leading to different levels of accuracy and sensitivity. Some software may prioritize speed, while others may prioritize accuracy, and still others may have specific strengths or limitations in handling certain types of data. It's important to carefully consider the characteristics and limitations of each software before making a choice to ensure the best possible alignment results Who sad this?

Riboviruses are a type of RNA virus that infect bacteria. They have a unique replication strategy, using the host bacteria's own machinery to replicate their RNA genome. Riboviruses are thought to have potential as therapeutic agents, as they can specifically target harmful bacteria while leaving beneficial bacteria unharmed. Some studies have even explored using riboviruses as a new way to treat antibiotic-resistant bacterial infections. Who sad this?

SLURM (Simple Linux Utility for Resource Management) is an open-source, highly scalable, and highly customizable cluster management and job scheduling system. It is widely used for managing high-performance computing (HPC) systems, allowing users to efficiently allocate resources, manage workloads, and monitor job progress. SLURM provides a simple and flexible interface for submitting, scheduling, and managing large-scale computing jobs, making it a popular choice for researchers, engineers, and other HPC users. Who sad this?

Trinity is a popular RNA-Seq assembly tool that can generate false positive results due to several reasons, such as incomplete or low-quality data, presence of genomic contaminants, low expression levels of certain transcripts, or technical artifacts. Improper usage of parameters and a lack of proper quality control can also lead to false positive results in the assembly process Who sad this?

The bacterial populations in UPW systems used in the semiconductor industry were studied, including 2 university and 4 full-scale industrial plants in different locations. Samples were taken from the polishing section, which can impact the quality of UPW used in the final stages of semiconductor production. These results provide an overview of the general bacterial diversity in UPW production. Who sad this?

To create a fasta file from a VCF file, use a script or software that can extract the genomic sequence information from the VCF file and format it into the fasta format. This allows you to generate a sequence-based representation of the genetic variation data stored in the VCF file, making it easier to visualize, analyze, and compare the variants. The fasta file can then be used as input for various bioinformatics tools and pipelines. Who sad this?

Genome annotations help us understand the functions and roles of genes and genomic regions, leading to improved knowledge of biological processes and disease mechanisms. Who sad this?

How to copy files in linux faster than cp

Disk mount in Linux refers to the process of making a file system available for the operating system to access on a particular directory. This is done by mounting the file system on a directory, which makes it accessible to the system and its users. Who said this?

Chip-Seq, Know to Unknown = =