Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

Statistics of local multiple alignments.

Amol Prakash1, Martin Tompa

  • 1Department of Computer Science and Engineering Box 352350 University of Washington Seattle, WA 98195-2350, USA. amol@cs.washington.edu

Bioinformatics (Oxford, England)
|June 18, 2005
PubMed
Summary
This summary is machine-generated.

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

A transcriptomic and proteomic map of primary human cell types.

Nucleic acids research·2026
Same author

Digging deeper into the immunopeptidome: characterization of post-translationally modified peptides presented by MHC I.

Journal of proteins and proteomics·2023
Same author

Reinspection of a Clinical Proteomics Tumor Analysis Consortium (CPTAC) Dataset with Cloud Computing Reveals Abundant Post-Translational Modifications and Protein Sequence Variants.

Cancers·2021
Same author

The utilization of the search engine, Bolt, to decrease search time and increase peptide identifications in hydroxyl radical protein footprinting-based workflows.

Proteomics·2021
Same author

Cloud Computing Based Immunopeptidomics Utilizing Community Curated Variant Libraries Simplifies and Improves Neo-Antigen Discovery in Metastatic Melanoma.

Cancers·2021
Same author

Quantitative assessment of successive carbohydrate additions to the clustered O-glycosylation sites of IgA1 by glycosyltransferases.

Glycobiology·2020
Same journal

Biomedical Concept Recognition with Error-aware Negative-enhanced Ranking Framework.

Bioinformatics (Oxford, England)·2026
Same journal

TEDLH: Domain HMMs for sensitive detection of remote homologues.

Bioinformatics (Oxford, England)·2026
Same journal

PLNFGL: Joint Estimation of Multi-Condition Gene Networks from Single-cell RNA-seq Data.

Bioinformatics (Oxford, England)·2026
Same journal

MCFST: Spatial domain identification method based on multi-view graph convolutional network and graph fusion network.

Bioinformatics (Oxford, England)·2026
Same journal

SpaBiT: Enhancing Spatial Transcriptomics Resolution via Bidirectional Attention Transformers.

Bioinformatics (Oxford, England)·2026
Same journal

EDEL: Enhancing Dense Retrievers for Curation of Biomedical Knowledge Bases.

Bioinformatics (Oxford, England)·2026
See all related articles

Researchers developed a new statistical score for multiple sequence alignments, extending BLAST theory. This score helps distinguish high-quality alignments from low-quality ones, improving biological sequence analysis.

Area of Science:

  • Bioinformatics
  • Computational Biology
  • Genomics

Background:

  • BLAST statistics are vital for pairwise sequence similarity searches.
  • Statistical scoring for multiple sequence alignments remains a challenge.
  • A standardized, well-founded score for multiple alignments is lacking.

Purpose of the Study:

  • To extend BLAST theory to develop a statistical score for multiple sequence alignments.
  • To provide a reliable method for assessing the quality of local multiple alignments.
  • To address the need for a standard statistical score in multiple alignment analysis.

Main Methods:

  • Extension of existing BLAST statistical theory.
  • Development of a novel significance score for local multiple alignment segments.

Related Experiment Videos

  • Experimental validation using orthologous vertebrate promoter sequences.
  • Main Results:

    • A new, justified significance score for multiple local alignment segments was successfully developed.
    • The proposed score effectively differentiates between high, moderate, and low-quality multiple alignments.
    • Experiments confirmed the score's utility in analyzing biological sequence data.

    Conclusions:

    • The new statistical score offers a robust method for evaluating multiple sequence alignments.
    • This advancement addresses a significant gap in current bioinformatics tools.
    • The score has practical applications in genomic research, particularly with promoter sequences.