"Molecular Sequence Data" 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.
Descriptions of specific amino acid, carbohydrate, or nucleotide sequences which have appeared in the published literature and/or are deposited in and maintained by databanks such as GENBANK, European Molecular Biology Laboratory (EMBL), National Biomedical Research Foundation (NBRF), or other sequence repositories.
| Descriptor ID |
D008969
|
| MeSH Number(s) |
L01.453.245.667
|
| Concept/Terms |
Molecular Sequence Data- Molecular Sequence Data
- Molecular Sequencing Data
- Data, Molecular Sequencing
- Sequencing Data, Molecular
- Sequence Data, Molecular
- Data, Molecular Sequence
|
Below are MeSH descriptors whose meaning is more general than "Molecular Sequence Data".
Below are MeSH descriptors whose meaning is more specific than "Molecular Sequence Data".
This graph shows the total number of publications written about "Molecular Sequence Data" by people in this website by year, and whether "Molecular Sequence Data" 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 | 6 | 6 |
| 1995 | 0 | 8 | 8 |
| 1996 | 0 | 8 | 8 |
| 1997 | 0 | 11 | 11 |
| 1998 | 0 | 6 | 6 |
| 1999 | 0 | 9 | 9 |
| 2000 | 0 | 7 | 7 |
| 2001 | 0 | 9 | 9 |
| 2002 | 0 | 6 | 6 |
| 2003 | 0 | 20 | 20 |
| 2004 | 0 | 11 | 11 |
| 2005 | 0 | 8 | 8 |
| 2006 | 0 | 17 | 17 |
| 2007 | 0 | 14 | 14 |
| 2008 | 0 | 17 | 17 |
| 2009 | 0 | 16 | 16 |
| 2010 | 0 | 13 | 13 |
| 2011 | 0 | 13 | 13 |
| 2012 | 0 | 19 | 19 |
| 2013 | 0 | 21 | 21 |
| 2014 | 0 | 19 | 19 |
| 2015 | 0 | 17 | 17 |
| 2016 | 0 | 1 | 1 |
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click here.
Below are the most recent publications written about "Molecular Sequence Data" by people in Profiles.
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A short conserved motif in ALYREF directs cap- and EJC-dependent assembly of export complexes on spliced mRNAs. Nucleic Acids Res. 2016 Mar 18; 44(5):2348-61.
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PEX6 is Expressed in Photoreceptor Cilia and Mutated in Deafblindness with Enamel Dysplasia and Microcephaly. Hum Mutat. 2016 Feb; 37(2):170-4.
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A novel homozygous splicing mutation of CASC5 causes primary microcephaly in a large Pakistani family. Hum Genet. 2016 Feb; 135(2):157-70.
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TRAIP promotes DNA damage response during genome replication and is mutated in primordial dwarfism. Nat Genet. 2016 Jan; 48(1):36-43.
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MINCR is a MYC-induced lncRNA able to modulate MYC's transcriptional network in Burkitt lymphoma cells. Proc Natl Acad Sci U S A. 2015 Sep 22; 112(38):E5261-70.
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De Novo Mutations in CHAMP1 Cause Intellectual Disability with Severe Speech Impairment. Am J Hum Genet. 2015 Sep 03; 97(3):493-500.
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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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Heterochrony underpins natural variation in Cardamine hirsuta leaf form. Proc Natl Acad Sci U S A. 2015 Aug 18; 112(33):10539-44.
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The Host as the Driver of the Microbiota in the Gut and External Environment of Drosophila melanogaster. Appl Environ Microbiol. 2015 Sep; 81(18):6232-40.
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Identification of a novel mutation in RIPK4 in a kindred with phenotypic features of Bartsocas-Papas and CHAND syndromes. Am J Med Genet A. 2015 Nov; 167A(11):2555-62.
MeSH information
