Related Experiment Video
Updated: Nov 8, 2025

10:36
Rare Event Detection Using Error-corrected DNA and RNA Sequencing
Published on: August 3, 2018
12.3K
iBLAST: Incremental BLAST of new sequences via automated e-value correction
Sajal Dash1,2, Sarthok Rasique Rahman3,4, Heather M Hines3,5
1National Center for Computational Sciences, Oak Ridge National Laboratory, Oak Ridge, TN, United States of America.
Plos One
|April 22, 2021
Summary
iBLAST reuses past BLAST search results to efficiently update sequence similarity searches on growing genomic databases. This method saves significant computational resources and time compared to rerunning full searches.
Area of Science:
- Bioinformatics
- Computational Biology
- Genomics
Background:
- Genomic databases are rapidly expanding, affecting the accuracy of sequence similarity search results.
- Traditional BLAST searches require rerunning against the entire updated database, wasting computational resources.
Purpose of the Study:
- To introduce iBLAST, a novel method for efficiently updating previous BLAST search results.
- To reduce the computational cost and time associated with re-analyzing large, growing genomic datasets.
Main Methods:
- iBLAST leverages existing BLAST results to query only the incremental portion of a growing database.
- It recomputes relevant statistics, such as expect values (e-values), and integrates them into updated results.
Main Results:
- iBLAST produces identical results to NCBI BLAST searches.
- The method offers substantial computational savings, performing (1 + δ)/δ times faster than NCBI BLAST, where δ is the database growth fraction.
Conclusions:
- iBLAST provides a highly efficient and cost-effective solution for updating genomic database searches.
- This approach enables faster biological discovery with reduced computational overhead.
Related Concept Videos
Mismatch Repair
42.4K
Overview
42.4K
Mismatch Repair
5.7K
Organisms are capable of detecting and fixing nucleotide mismatches that occur during DNA replication. This sophisticated process requires identifying the new strand and replacing the erroneous bases with correct nucleotides. Mismatch repair is coordinated by many proteins in both prokaryotes and eukaryotes.
The Mutator Protein Family Plays a Key Role in DNA Mismatch Repair
The human genome has more than 3 billion base pairs of DNA per cell. Prior to cell division, that vast amount of genetic...
The Mutator Protein Family Plays a Key Role in DNA Mismatch Repair
The human genome has more than 3 billion base pairs of DNA per cell. Prior to cell division, that vast amount of genetic...
5.7K
Next-generation Sequencing
95.4K
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....
Next-Generation Sequencing Methods
Although all next-generation methods use different technologies, they all share a set of standard features....
95.4K
Gene Evolution - Fast or Slow?
7.7K
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...
In contrast, regions which code...
7.7K
Evolutionary Relationships through Genome Comparisons
6.5K
Genome comparison is one of the excellent ways to interpret the evolutionary relationships between organisms. The basic principle of genome comparison is that if two species share a common feature, it is likely encoded by the DNA sequence conserved between both species. The advent of genome sequencing technologies in the late 20th century enabled scientists to understand the concept of conservation of domains between species and helped them to deduce evolutionary relationships across diverse...
6.5K

