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Related Concept Videos

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.
Next-generation Sequencing03:00

Next-generation Sequencing

The first human genome sequencing project cost $2.7 billion and was declared complete in 2003, after 15 years of international cooperation and collaboration between several research teams and funding agencies. Today, with the advent of next-generation sequencing technologies, the cost and time of sequencing a human genome have dropped over 100 fold.
Next-Generation Sequencing Methods
Although all next-generation methods use different technologies, they all share a set of standard features.
Oligosaccharide Assembly01:24

Oligosaccharide Assembly

Protein glycosylation starts in the ER lumen and continues in the Golgi apparatus. Glycosyltransferases catalyze the addition of sugar molecules or glycosylation of proteins. Usually, these enzymes add sugars to the hydroxyl groups of selected serine or threonine residues to form O-linked glycans or the amino groups of asparagine residues to form N-linked glycans. Different positions on the same polypeptide chain can contain differently linked glycans.
Multiple sugar molecules that may or may...
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...
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...
RACE - Rapid Amplification of cDNA Ends02:35

RACE - Rapid Amplification of cDNA Ends

Rapid Amplification of cDNA Ends, or RACE, is one of the most effective methods to obtain a full-length cDNA from an mRNA sequence between a known internal region to the unknown sequence at the 5’ or 3’ end. The unknown region is cloned in the cDNA by a gene-specific primer that binds the known end, and a hybrid primer that attaches a predefined anchor sequence to the unknown end of the cDNA. The sequence in between is amplified by PCR with an anchor primer and a gene-specific primer.
Since the...

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Updated: May 22, 2026

Leveraging CyVerse Resources for De Novo Comparative Transcriptomics of Underserved (Non-model) Organisms
10:41

Leveraging CyVerse Resources for De Novo Comparative Transcriptomics of Underserved (Non-model) Organisms

Published on: May 9, 2017

Gossamer--a resource-efficient de novo assembler.

Thomas Conway1, Jeremy Wazny, Andrew Bromage

  • 1NICTA Victoria Research Laboratory, Department of Computing and Information Systems, The University of Melbourne, Parkville, Victoria 3010, Australia. tom.conway@nicta.com.au

Bioinformatics (Oxford, England)
|May 22, 2012
PubMed
Summary
This summary is machine-generated.

Gossamer is a new tool for de novo assembly of short-read sequencing data. It efficiently produces high-quality genome assemblies with minimal memory usage.

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12:08

Hybrid De Novo Genome Assembly for the Generation of Complete Genomes of Urinary Bacteria using Short- and Long-read Sequencing Technologies

Published on: August 20, 2021

Area of Science:

  • Genomics
  • Bioinformatics

Background:

  • De novo assembly of short-read high-throughput sequencing data presents significant computational challenges due to large data volumes, small read lengths, and sequencing errors.
  • Existing short-read assemblers are often limited to smaller genomes or require substantial computing resources, frequently yielding suboptimal results.
  • Many current assembly algorithms employ greedy approaches, which can compromise the quality of the final genome assembly.

Purpose of the Study:

  • To develop a novel computational tool for efficient and high-quality de novo assembly of short-read sequencing data.
  • To address the memory and computational limitations of existing genome assembly software.
  • To provide a space-efficient and effective solution for assembling large and complex genomes.

Main Methods:

  • Implementation of the de Bruijn graph approach for sequence assembly.
  • Development of Gossamer, a software package designed for efficient processing of large sequencing datasets.
  • Optimization of memory usage to approach theoretical minimums for de novo assembly.

Main Results:

  • Gossamer demonstrates significant space efficiency, requiring minimal memory for operation.
  • The software enables efficient processing of high-throughput sequencing data.
  • Gossamer produces high-quality genome assemblies, outperforming existing methods in terms of accuracy and completeness.

Conclusions:

  • Gossamer offers a computationally efficient and memory-sparing solution for de novo genome assembly.
  • The tool is capable of generating high-quality assemblies from short-read sequencing data.
  • Gossamer provides a valuable resource for researchers dealing with large-scale genomic data analysis.