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Related Concept Videos

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...
Genomic DNA in Eukaryotes00:58

Genomic DNA in Eukaryotes

Eukaryotes have large genomes compared to prokaryotes. To fit their genomes into a cell, eukaryotic DNA is packaged extraordinarily tightly inside the nucleus. To achieve this, DNA is tightly wound around proteins called histones, which are packaged into nucleosomes that are joined by linker DNA and coil into chromatin fibers. Additional fibrous proteins further compact the chromatin, which is recognizable as chromosomes during certain phases of cell division.
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.
Sanger Sequencing01:57

Sanger Sequencing

DNA sequencing is a fundamental technique that is routinely used in the biological sciences. This method can be applied to a range of questions at different scales - from the sequencing of a cloned DNA fragment or the study of a mutation in a gene up to whole-genome sequencing. However, despite the widespread use of sequencing today, it was not until 1977 that Fredrick Sanger and his collaborators developed the chain-termination method to decode DNA sequences. It relies on the separation of a...
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...

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Related Experiment Video

Updated: Jun 18, 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

ENCODE whole-genome data in the UCSC Genome Browser.

Kate R Rosenbloom1, Timothy R Dreszer, Michael Pheasant

  • 1Center for Biomolecular Science and Engineering, School of Engineering, University of California, Santa Cruz, CA 95064, USA. kate@soe.ucsc.edu

Nucleic Acids Research
|November 19, 2009
PubMed
Summary
This summary is machine-generated.

The Encyclopedia of DNA Elements (ENCODE) project catalogs functional elements in the human genome. Data is accessible via the UCSC Genome Browser and web portal for research and data mining.

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Last Updated: Jun 18, 2026

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Area of Science:

  • Genomics
  • Bioinformatics

Background:

  • The human genome contains numerous functional elements.
  • Understanding these elements is crucial for biological research.

Purpose of the Study:

  • To create a comprehensive catalog of functional elements in the human genome.
  • To provide accessible data and tools for analyzing genomic information.

Main Methods:

  • International collaboration of researchers.
  • Data generation and analysis through the ENCODE project.
  • Centralized data repository and bioinformatics tools at UC Santa Cruz.

Main Results:

  • Establishment of the ENCODE Data Coordination Center.
  • Development of the UCSC Genome Bioinformatics database.
  • Availability of the UCSC Genome Browser for data visualization and mining.

Conclusions:

  • The ENCODE project provides a valuable resource for human genome research.
  • Accessible data and tools facilitate the study of functional genomic elements.