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Related Concept Videos

Genetic Screens02:46

Genetic Screens

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Genetic screens are tools used to identify genes and mutations responsible for phenotypes of interest. Genetic screens help identify individuals or a group of people at risk of developing  genetic diseases and help them with early intervention, targeted therapy, and reproductive options.
Forward genetic screens
Forward or “classical” genetic screens involve creating random mutations in an organism’s DNA using radiation, mutagens, or insertion of additional bases, which...
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Modified Boxplots00:57

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A standard box and whisker plot informs us about the spread of the data in a given sample. One can identify the minimum value, maximum value, first quartile value, second quartile or median value, and third quartile.
However, the box plot does not tell the reader about outliers - values that lie far from the center of the data. We can modify the standard box and whisker plot to identify the outliers and visualize the actual spread of the data in a sample.
Initially, we calculate the adjusted...
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DNA Microarrays02:34

DNA Microarrays

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Microarrays are high-throughput and relatively inexpensive assays that can be automated to analyze large quantities of data at a time. They are used in genome-wide studies to compare gene or protein expression under two varied conditions, such as healthy and diseased states. Microarrays consist of glass or silica slides on which probe molecules are covalently attached through surface functionalization. Most commonly, the slides are prepared through the chemisorption of silanes to silica...
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Residual Plots01:07

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A residual plot is a statistical representation of data used to analyze correlation and regression results. It helps verify the requirements for drawing specific conclusions about correlation and regression. To obtain the residual plot, first, the residual for each data value is calculated, which is simply the vertical distance between the observed and the predicted value obtained from the regression equation.
When the residual values are plotted against the variable x, it is called a residual...
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Comparing Copy Number Variations and SNPs02:26

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Sequencing of the human genome has opened up several best-kept secrets of the genome. Scientists have identified thousands of genome variations that exist within a population. These variations can be a single nucleotide or a larger chromosomal variation.
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Genome Copying Errors02:46

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DNA replication is a well-evolved process that copies millions of base pairs with high fidelity during each cell division. Occasionally a wrong base or a long stretch of wrong bases may get added to the daughter strands. If the errors are left unchecked, cells might accumulate several mutations that might endanger their  survival. Therefore, the copying errors are checked and repaired at three levels.
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Updated: Dec 13, 2025

A Robust Polymerase Chain Reaction-based Assay for Quantifying Cytosine-guanine-guanine Trinucleotide Repeats in Fragile X Mental Retardation-1 Gene
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pyGenomeTracks: reproducible plots for multivariate genomic datasets.

Lucille Lopez-Delisle1, Leily Rabbani2, Joachim Wolff3

  • 1UPDUB, ISREC Department, School of Life Sciences (SV), EPFL, 1015 Lausanne, Switzerland.

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Generating publication-ready genomic track plots is challenging. pyGenomeTracks (PGT) offers a reproducible and customizable solution for creating complex figures efficiently.

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Area of Science:

  • Genomics
  • Bioinformatics
  • Computational Biology

Background:

  • Generating publication-quality figures for multiple genomic tracks is complex and time-consuming.
  • Manual figure creation or reliance on vector graphics software requires significant effort and expertise.

Purpose of the Study:

  • To introduce pyGenomeTracks (PGT) as a modular tool for simplifying the generation of genomic track plots.
  • To enable reproducible and standardized creation of customizable, publication-ready genomic visualizations.

Main Methods:

  • PGT is a modular plotting tool designed for combining multiple genomic tracks.
  • The tool facilitates the generation of highly customizable and publication-ready images.

Main Results:

  • pyGenomeTracks enables the easy combination of multiple genomic tracks.
  • It supports reproducible and standardized generation of complex figures.

Conclusions:

  • PGT simplifies the creation of publication-ready genomic track plots.
  • The tool enhances reproducibility and customization in genomic data visualization.