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Related Concept Videos

Next-generation Sequencing03:00

Next-generation Sequencing

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.
Sanger Sequencing01:57

Sanger Sequencing

DNA sequencing is a fundamental technique that is routinely used in the biological sciences. This method can be applied to a range of questions at different scales - from the sequencing of a cloned DNA fragment or the study of a mutation in a gene up to whole-genome sequencing. However, despite the widespread use of sequencing today, it was not until 1977 that Fredrick Sanger and his collaborators developed the chain-termination method to decode DNA sequences. It relies on the separation of a...
Maxam-Gilbert Sequencing01:05

Maxam-Gilbert Sequencing

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
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RNA-seq03:21

RNA-seq

RNA sequencing, or RNA-Seq, is a high-throughput sequencing technology used to study the transcriptome of a cell. Transcriptomics helps to interpret the functional elements of a genome and identify the molecular constituents of an organism. Additionally, it also helps in understanding the development of an organism and the occurrence of diseases. 
Before the discovery of RNA-seq, microarray-based methods and Sanger sequencing were used for transcriptome analysis. However, while microarray-based...
Signal Sequences and Sorting Receptors01:41

Signal Sequences and Sorting Receptors

Signal sequences are short amino acid sequences that guide newly synthesized proteins to their proper location within the cell. Classical signal sequences are fifteen to sixty amino acids long and present at the N-terminus of a polypeptide chain. Each signal sequence has a conserved segment of basic residues towards their N terminus, a hydrophobic core, and a C-terminus rich in polar residues. The C-terminus also contains a signal cleavage site and features a -3 -1 sequence motif. The -3-1...

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Related Experiment Video

Updated: Jul 3, 2026

Rare Event Detection Using Error-corrected DNA and RNA Sequencing
10:36

Rare Event Detection Using Error-corrected DNA and RNA Sequencing

Published on: August 3, 2018

Sequence search algorithms for single pass sequence identification: does one size fit all?

K C Woodwark1, S J Hubbard, S G Oliver

  • 1Department of Biomolecular Sciences UMIST, Manchester M60 1QD, UK.

Comparative and Functional Genomics
|July 17, 2008
PubMed
Summary
This summary is machine-generated.

Choosing the right parameters for BLAST sequence searches is crucial. Default settings in NCBI

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Related Experiment Videos

Last Updated: Jul 3, 2026

Rare Event Detection Using Error-corrected DNA and RNA Sequencing
10:36

Rare Event Detection Using Error-corrected DNA and RNA Sequencing

Published on: August 3, 2018

Exploring Sequence Space to Identify Binding Sites for Regulatory RNA-Binding Proteins
11:34

Exploring Sequence Space to Identify Binding Sites for Regulatory RNA-Binding Proteins

Published on: August 9, 2019

DNA Sequence Recognition by DNA Primase Using High-Throughput Primase Profiling
08:04

DNA Sequence Recognition by DNA Primase Using High-Throughput Primase Profiling

Published on: October 8, 2019

Area of Science:

  • Bioinformatics
  • Genomics
  • Computational Biology

Background:

  • The rapid increase in biological sequence data necessitates efficient analysis tools.
  • Single-pass sequences, like expressed sequence tags (ESTs), often contain errors complicating homology identification.
  • Nucleotide-level sequence searches are common for analyzing such data.

Purpose of the Study:

  • To evaluate the performance of different BLAST algorithm versions for comparing sample sequence datasets to a known genome.
  • To identify the impact of parameter choices on BLAST search results.

Main Methods:

  • Comparison of sequence alignments generated by Washington University's BLASTn and NCBI's gapped BLASTn.
  • Analysis of default parameter settings in both BLAST versions.
  • Benchmarking against the Smith-Waterman algorithm.

Main Results:

  • NCBI's gapped BLASTn with default parameters produced shorter and sometimes different top alignments compared to Washington University's BLASTn.
  • Parameter choices, not algorithmic differences, were the primary cause of performance variations.
  • Washington University's BLASTn with default parameters showed favorable comparison to the Smith-Waterman algorithm.

Conclusions:

  • Careful selection of BLAST parameters is essential for accurate sequence data analysis.
  • Washington University's BLASTn offers a practical and effective tool for genomic comparisons.
  • Default parameters significantly influence the outcome of sequence homology searches.