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Related Concept Videos

Genomics02:02

Genomics

Genomics is the science of genomes: it is the study of all the genetic material of an organism. In humans, the genome consists of information carried in 23 pairs of chromosomes in the nucleus, as well as mitochondrial DNA. In genomics, both coding and non-coding DNA is sequenced and analyzed. Genomics allows a better understanding of all living things, their evolution, and their diversity. It has a myriad of uses: for example, to build phylogenetic trees, to improve productivity and...
Genome Annotation and Assembly03:36

Genome Annotation and Assembly

The genome refers to all of the genetic material in an organism. It can range from a few million base pairs in microbial cells to several billion base pairs in many eukaryotic organisms. Genome assembly refers to the process of taking the DNA sequencing data and putting it all back together in a correct order to create a close representation of the original genome. This is followed by the identification of functional elements on the newly assembled genome, a process called genome annotation.
Evolutionary Relationships through Genome Comparisons02:54

Evolutionary Relationships through Genome Comparisons

Genome comparison is one of the excellent ways to interpret the evolutionary relationships between organisms. The basic principle of genome comparison is that if two species share a common feature, it is likely encoded by the DNA sequence conserved between both species. The advent of genome sequencing technologies in the late 20th century enabled scientists to understand the concept of conservation of domains between species and helped them to deduce evolutionary relationships across diverse...
Genome-wide Association Studies-GWAS01:11

Genome-wide Association Studies-GWAS

Genome-wide association studies or GWAS are used to identify whether common SNPs are associated with certain diseases. Suppose specific SNPs are more frequently observed in individuals with a particular disease than those without the disease. In that case, those SNPs are said to be associated with the disease. Chi-square analysis is performed to check the probability of the allele likely to be associated with the disease.
GWAS does not require the identification of the target gene involved in...

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Related Experiment Video

Updated: May 19, 2026

An Integrated Approach for Microprotein Identification and Sequence Analysis
09:37

An Integrated Approach for Microprotein Identification and Sequence Analysis

Published on: July 12, 2022

The UCSC genome browser and associated tools.

Robert M Kuhn1, David Haussler, W James Kent

  • 1Center for Biomolecular Science and Engineering, University of California, Santa Cruz, 1156 High Street, Santa Cruz, CA 95064, USA. kuhn@soe.ucsc.edu

Briefings in Bioinformatics
|August 22, 2012
PubMed
Summary
This summary is machine-generated.

The UCSC Genome Browser provides integrated genomic data visualization for 58 organisms, supporting diverse data types and high-throughput sequencing experiments. It facilitates data mining and sharing through tools like BLAT and Custom Tracks.

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Area of Science:

  • Genomics
  • Bioinformatics
  • Data Visualization

Background:

  • The UCSC Genome Browser has been a key resource for genomic data visualization for over a decade.
  • It integrates diverse genomic datasets, including gene predictions, epigenomic data, and variation data.

Purpose of the Study:

  • To provide an updated overview of the UCSC Genome Browser's capabilities and features.
  • To highlight its utility for inquiry-driven data mining and analysis of large-scale sequencing data.

Main Methods:

  • Visualization of genomic annotations mapped to genomic coordinates for 58 organisms.
  • Integration of diverse data types including gene predictions, mRNA alignments, epigenomic data (ENCODE), conservation scores, and variation data.
  • Support for uploading private data via Custom Tracks and Data Hubs, and visualization of high-throughput sequencing data formats (BAM, VCF, SNP).

Main Results:

  • The Browser offers visualization from single base to entire chromosome scale.
  • Tools like BLAT, Table Browser, and Saved Sessions enhance data analysis and sharing.
  • Support for compact, indexed formats (BAM, bigBed, bigWig) enables rapid visualization of large datasets from RNA-seq and ChIP-seq experiments.

Conclusions:

  • The UCSC Genome Browser remains a comprehensive and versatile platform for genomic data exploration and analysis.
  • Its continuous development supports modern high-throughput sequencing and facilitates collaborative research through data sharing features.