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Related Concept Videos

Per-Unit Sequence Models01:26

Per-Unit Sequence Models

185
An ideal Y-Y transformer, grounded through neutral impedances, displays per-unit sequence networks akin to those of a single-phase ideal transformer when subjected to balanced positive- or negative-sequence currents. These currents do not produce neutral currents, and their associated voltage drops.
Zero-sequence currents, which are identical in magnitude and phase, generate a neutral current, resulting in voltage drops across the neutral impedance and the low-voltage winding. If the...
185
Sequence Networks of Rotating Machines01:24

Sequence Networks of Rotating Machines

218
A Y-connected synchronous generator, grounded through a neutral impedance, is designed to produce balanced internal phase voltages with only positive-sequence components. The generator's sequence networks include a source voltage that is exclusively in the positive-sequence network. The sequence components of line-to-ground voltages at the generator terminals illustrate this configuration.
Zero-sequence current induces a voltage drop across the generator's neutral impedance and other...
218
Maxam-Gilbert Sequencing01:05

Maxam-Gilbert Sequencing

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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.
Challenges of the Maxam-Gilbert Method
The...
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Next-generation Sequencing03:00

Next-generation Sequencing

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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....
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DNA as a Genetic Template02:05

DNA as a Genetic Template

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Two structural features of the DNA molecule provide a basis for the mechanisms of heredity: the four nucleotide bases and its double-stranded nature. The Watson-Crick model of double-helical DNA structure, proposed in 1952, drew heavily upon the X-ray crystallography work of researchers Rosalind Franklin and Maurice Wilkins. Watson, Crick, and Wilkins jointly received the Nobel Prize in Physiology or Medicine for their work in 1962. Franklin was, controversially, excluded from the prize for...
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Genome Annotation and Assembly03:36

Genome Annotation and Assembly

19.7K
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.
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Updated: Nov 4, 2025

A Virtual Machine Platform for Non-Computer Professionals for Using Deep Learning to Classify Biological Sequences of Metagenomic Data
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A Virtual Machine Platform for Non-Computer Professionals for Using Deep Learning to Classify Biological Sequences of Metagenomic Data

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Protein sequence design with deep generative models.

Zachary Wu1, Kadina E Johnston2, Frances H Arnold3

  • 1Division of Chemistry and Chemical Engineering, California Institute of Technology, 1200 E California Blvd, Pasadena, 91125, CA, USA.

Current Opinion in Chemical Biology
|May 29, 2021
PubMed
Summary
This summary is machine-generated.

Machine learning, particularly deep generative models, is revolutionizing protein engineering. These advanced methods accelerate the discovery of novel protein sequences with desired functions by leveraging existing data and experimental insights.

Keywords:
Deep learningGenerative modelsProtein engineering

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Area of Science:

  • Biochemistry and Molecular Biology
  • Computational Biology
  • Artificial Intelligence in Life Sciences

Background:

  • Protein engineering aims to design proteins with enhanced or novel functions.
  • Traditional protein design methods are often labor-intensive and time-consuming.
  • Machine learning (ML) offers powerful tools to accelerate protein sequence generation.

Purpose of the Study:

  • To review recent advancements in ML-guided protein sequence generation.
  • To highlight the role of deep generative models in protein engineering.
  • To provide an overview of current trends and future directions in the field.

Main Methods:

  • Literature review of recent research publications.
  • Focus on deep generative models, including variational autoencoders and generative adversarial networks.
  • Analysis of ML approaches applied to protein sequence design.

Main Results:

  • ML significantly enhances the efficiency and success rate of protein sequence generation.
  • Deep generative models show particular promise for de novo protein design.
  • Integration of ML with experimental data improves model accuracy and predictive power.

Conclusions:

  • Machine learning, especially deep generative methods, is transforming protein engineering.
  • These computational approaches enable the rapid design of proteins with tailored properties.
  • The synergy between ML and experimental validation is crucial for future breakthroughs in protein design.