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Related Concept Videos

Improving Translational Accuracy02:07

Improving Translational Accuracy

Base complementarity between the three base pairs of mRNA codon and the tRNA anticodon is not a failsafe mechanism. Inaccuracies can range from a single mismatch to no correct base pairing at all. The free energy difference between the correct and nearly correct base pairs can be as small as 3 kcal/ mol. With complementarity being the only proofreading step, the estimated error frequency would be one wrong amino acid in every 100 amino acids incorporated. However, error frequencies observed in...
Improving Translational Accuracy02:07

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Base complementarity between the three base pairs of mRNA codon and the tRNA anticodon is not a failsafe mechanism. Inaccuracies can range from a single mismatch to no correct base pairing at all. The free energy difference between the correct and nearly correct base pairs can be as small as 3 kcal/ mol. With complementarity being the only proofreading step, the estimated error frequency would be one wrong amino acid in every 100 amino acids incorporated. However, error frequencies observed in...
Central Limit Theorem01:14

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The central limit theorem, abbreviated as clt, is one of the most powerful and useful ideas in all of statistics. The central limit theorem for sample means says that if you repeatedly draw samples of a given size and calculate their means, and create a histogram of those means, then the resulting histogram will tend to have an approximate normal bell shape. In other words, as sample sizes increase, the distribution of means follows the normal distribution more closely.
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Highly Multiplexed, Super-resolution Imaging of T Cells Using madSTORM
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Published on: June 24, 2017

New finite-size correction for local alignment score distributions.

Yonil Park1, Sergey Sheetlin, Ning Ma

  • 1National Center for Biotechnology Information, National Library of Medicine, Bethesda, MD 20894, USA.

BMC Research Notes
|June 14, 2012
PubMed
Summary

A new finite-size correction improves local alignment probability calculations by considering sequence length distributions. This enhances sensitivity, particularly for shorter sequences, and is now integrated into BLAST+ and NCBI BLAST.

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Area of Science:

  • Bioinformatics
  • Computational Biology
  • Sequence Analysis

Background:

  • Local alignment algorithms assess match significance by calculating probabilities.
  • Accurate probability calculation may require finite-size corrections for sequence lengths.
  • Alignments near sequence ends can be affected by limited sequence availability.

Purpose of the Study:

  • To develop an improved finite-size correction method for local alignment probability calculations.
  • To enhance the sensitivity and accuracy of statistical significance assessment in sequence alignments.
  • To address limitations in current methods, especially for shorter sequences.

Main Methods:

  • Developed a novel finite-size correction considering the distribution of sequence lengths.
  • Utilized a test set derived from the ASTRAL database for evaluation.
  • Assessed performance using Receiver Operating Characteristic (ROC) scores.

Main Results:

  • The improved correction enhances sensitivity and avoids underestimation of significance for short sequences.
  • Demonstrated improved ROC scores, particularly for shorter sequences, compared to existing methods.
  • The new method provides a more accurate assessment of local alignment probabilities.

Conclusions:

  • The refined finite-size correction significantly improves local alignment probability calculations.
  • This advancement enhances the reliability of statistical significance assessment in sequence analysis.
  • The improved method is now implemented in the widely used BLAST+ package and the NCBI BLAST web service.