"Sequence Alignment" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
The arrangement of two or more amino acid or base sequences from an organism or organisms in such a way as to align areas of the sequences sharing common properties. The degree of relatedness or homology between the sequences is predicted computationally or statistically based on weights assigned to the elements aligned between the sequences. This in turn can serve as a potential indicator of the genetic relatedness between the organisms.
| Descriptor ID |
D016415
|
| MeSH Number(s) |
E05.393.751
|
| Concept/Terms |
Sequence Alignment- Sequence Alignment
- Alignment, Sequence
- Alignments, Sequence
- Sequence Alignments
Determination, Sequence Homology- Determination, Sequence Homology
- Determinations, Sequence Homology
- Sequence Homology Determinations
- Sequence Homology Determination
|
Below are MeSH descriptors whose meaning is more general than "Sequence Alignment".
Below are MeSH descriptors whose meaning is more specific than "Sequence Alignment".
This graph shows the total number of publications written about "Sequence Alignment" by people in this website by year, and whether "Sequence Alignment" was a major or minor topic of these publications.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 1994 | 0 | 2 | 2 |
| 1997 | 0 | 2 | 2 |
| 1999 | 0 | 2 | 2 |
| 2001 | 0 | 2 | 2 |
| 2002 | 1 | 0 | 1 |
| 2003 | 5 | 2 | 7 |
| 2004 | 1 | 3 | 4 |
| 2005 | 0 | 2 | 2 |
| 2006 | 3 | 5 | 8 |
| 2007 | 2 | 1 | 3 |
| 2008 | 2 | 5 | 7 |
| 2009 | 3 | 5 | 8 |
| 2010 | 1 | 1 | 2 |
| 2011 | 1 | 5 | 6 |
| 2012 | 0 | 4 | 4 |
| 2013 | 1 | 5 | 6 |
| 2014 | 0 | 4 | 4 |
| 2015 | 1 | 4 | 5 |
| 2017 | 0 | 2 | 2 |
| 2018 | 1 | 1 | 2 |
| 2019 | 0 | 1 | 1 |
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Below are the most recent publications written about "Sequence Alignment" by people in Profiles.
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Complementing the intrinsic repertoire of Ustilago maydis for degradation of the pectin backbone polygalacturonic acid. J Biotechnol. 2020 Jan 10; 307:148-163.
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Recombination Signal in Mycobacterium tuberculosis Stems from Reference-guided Assemblies and Alignment Artefacts. Genome Biol Evol. 2018 08 01; 10(8):1920-1926.
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VIPER: Visualization Pipeline for RNA-seq, a Snakemake workflow for efficient and complete RNA-seq analysis. BMC Bioinformatics. 2018 04 12; 19(1):135.
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Sample Size Estimation for Detection of Splicing Events in Transcriptome Sequencing Data. Int J Mol Sci. 2017 Sep 05; 18(9).
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Validation of Splicing Events in Transcriptome Sequencing Data. Int J Mol Sci. 2017 May 23; 18(6).
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Conserved and unique features of the homeologous maize Aux/IAA proteins ROOTLESS WITH UNDETECTABLE MERISTEM 1 and RUM1-like 1. J Exp Bot. 2016 Feb; 67(4):1137-47.
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WDR73 Mutations Cause Infantile Neurodegeneration and Variable Glomerular Kidney Disease. Hum Mutat. 2015 Nov; 36(11):1021-8.
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Denoising DNA deep sequencing data-high-throughput sequencing errors and their correction. Brief Bioinform. 2016 Jan; 17(1):154-79.
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Suppression of early hematogenous dissemination of human breast cancer cells to bone marrow by retinoic Acid-induced 2. Cancer Discov. 2015 May; 5(5):506-19.
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rbamtools: an R interface to samtools enabling fast accumulative tabulation of splicing events over multiple RNA-seq samples. Bioinformatics. 2015 May 15; 31(10):1663-4.
MeSH information
