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Related Concept Videos

Maxam-Gilbert Sequencing01:05

Maxam-Gilbert Sequencing

In the same year as the discovery of the Sanger sequencing method, another group of scientists, Allan Maxam and Walter Gilbert, demonstrated their chemical-cleavage method for DNA sequencing. The Maxam-Gilbert method relies on using different chemicals that can cleave the DNA sequence at specific sites, the separation of resulting DNA fragments of variable size using electrophoresis, and deciphering the DNA sequence from the resulting gel bands.
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Multi-species Conserved Sequences02:51

Multi-species Conserved Sequences

Next-generation sequencing technologies have created large genomic databases of a variety of animals and plants. Ever since the human genome project was completed, scientists studied the genome of primates, mammals, and other phylogenetically distant living beings. Such large-scale  studies have provided new insights into the evolutionary relationship between organisms.
Although the genome of each species varies greatly from each other, a few sequences are highly conserved. Such conserved DNA...
Conservation of Protein Domains Over Different Proteins02:26

Conservation of Protein Domains Over Different Proteins

Protein domains are small structurally independent units that are part of a single amino acid chain.  Although these domains are often structurally independent, they may rely on synergistic effects to perform their functions as part of a larger protein. Protein domains may be conserved within the same organism, as well as across different organisms.
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Gene Duplication and Divergence02:37

Gene Duplication and Divergence

The seminal work of Ohno in 1970 popularized the idea of gene duplication and divergence. DNA sequence comparison studies reveal that a large portion of the genes in bacteria, archaebacteria, and eukaryotes was  generated by gene duplication and divergence, indicating its critical role in evolution.
The duplicated copies of the gene are called Paralogs. Paralogs with similar sequences and functions form a gene family. Across several species, a large number of gene families are characterized.
Gene Evolution - Fast or Slow?02:05

Gene Evolution - Fast or Slow?

The genomes of eukaryotes are punctuated by long stretches of sequence which do not code for proteins or RNAs. Although some of these regions do contain crucial regulatory sequences, the vast majority of this DNA serves no known function. Typically, these regions of the genome are the ones in which the fastest change, in evolutionary terms, is observed, because there is typically little to no selection pressure acting on these regions to preserve their sequences.
In contrast, regions which code...
Gene Evolution - Fast or Slow?02:05

Gene Evolution - Fast or Slow?

The genomes of eukaryotes are punctuated by long stretches of sequence which do not code for proteins or RNAs. Although some of these regions do contain crucial regulatory sequences, the vast majority of this DNA serves no known function. Typically, these regions of the genome are the ones in which the fastest change, in evolutionary terms, is observed, because there is typically little to no selection pressure acting on these regions to preserve their sequences.
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Related Experiment Video

Updated: Jun 19, 2026

Optimization of Synthetic Proteins: Identification of Interpositional Dependencies Indicating Structurally and/or Functionally Linked Residues
07:08

Optimization of Synthetic Proteins: Identification of Interpositional Dependencies Indicating Structurally and/or Functionally Linked Residues

Published on: July 14, 2015

Heuristic reusable dynamic programming: efficient updates of local sequence alignment.

Changjin Hong1, Ahmed H Tewfik

  • 1Department of Electrical Engineering, University of Minnesota, 4-192 EE/CSCI Building, 200 Union St. SE, Minneapolis, MN 55455, USA. hong@cs.umn.edu

IEEE/ACM Transactions on Computational Biology and Bioinformatics
|October 31, 2009
PubMed
Summary
This summary is machine-generated.

Updating biological sequence similarity results is crucial for accuracy. This study presents an efficient method for updating local sequence alignments, significantly reducing computational costs and improving accuracy using heuristic searching bands and reusable dynamic programming.

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Area of Science:

  • Bioinformatics
  • Computational Biology
  • Genomics

Background:

  • Recomputing biological sequence similarity is essential due to data errors or comparing highly similar sequences.
  • Existing methods can be computationally intensive, especially for large datasets or frequent updates.

Purpose of the Study:

  • To develop an efficient scheme for updating local sequence alignments with an affine gap model.
  • To accelerate the recomputation process by leveraging previous alignment results and heuristic approaches.

Main Methods:

  • Utilizing forward-backward alignment to generate heuristic searching bands based on suboptimal paths.
  • Implementing a confined Smith-Waterman algorithm within these bands.
  • Validating the relative node tolerance bound (RNTB) and integrating reusable dynamic programming (rDP) for further acceleration.
  • Quantifying RNTB tolerance probability and selectively applying rDP to perturbation-resilient columns.

Main Results:

  • The proposed heuristic alignment method significantly reduces computational runtime compared to standard and sparse dynamic programming.
  • Achieved 98.3% accuracy in correctly updated paths within a 90% optimal alignment score threshold.
  • Runtime cost was reduced to 25.36% of sparse dynamic programming (sDP) and 2.55% of the standard Smith-Waterman algorithm.

Conclusions:

  • The developed scheme provides an efficient and accurate method for updating local sequence alignments.
  • The integration of RNTB and selective rDP application offers substantial computational performance improvements.
  • This approach is valuable for researchers dealing with sequence data errors or needing to compare closely related biological sequences.