Database Commons
Database Commons

a catalog of worldwide biological databases

Database Profile

General information

URL: http://cefg.uestc.edu.cn/smal
Full name: Spontaneous Mutation Accumulation Lines.
Description: A Resource of Spontaneous Mutation Accumulation Lines.Mutation is the ultimate source of genetic variation and evolution. Mutation accumulation (MA) experiments are an alternative approach to study de novo mutation events directly
Year founded: 2014
Last update: 2014
Version:
Accessibility:
Manual:
Accessible
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Country/Region: China

Classification & Tag

Data type:
DNA
Data object:
Database category:
Major species:
Keywords:

Contact information

University/Institution: University of Electronic Science and Technology of China
Address: Center of Bioinformatics, Key Laboratory for NeuroInformation of the Ministry of Education, University of Electronic Science and Technology of China, Chengdu, China
City: Chengdu
Province/State: Sichuan
Country/Region: China
Contact name (PI/Team): Feng-Biao Guo
Contact email (PI/Helpdesk): fbguo@uestc.edu.cn.fbguo@uestc.edu.cn.

Publications

24531082
SMAL: A Resource of Spontaneous Mutation Accumulation Lines. [PMID: 24531082]
Wei W, Ning LW, Ye YN, Li SJ, Zhou HQ, Huang J, Guo FB.

Mutation is the ultimate source of genetic variation and evolution. Mutation accumulation (MA) experiments are an alternative approach to study de novo mutation events directly. We have constructed a resource of Spontaneous Mutation Accumulation Lines (SMAL; http://cefg.uestc.edu.cn/smal), which contains all the current publicly available MA lines identified by high-throughput sequencing. We have relocated and mapped the mutations based on the most recent genome annotations. A total of 5,608 single base mutations and 540 other mutations were obtained and are recorded in the current version of the SMAL database. The integrated data in SMAL provide detailed information that can be used in new theoretical analyses. We believe that the SMAL resource will help researchers better understand the processes of genetic variation and the incidence of disease.

Mol Biol Evol. 2014:31(5) | 6 Citations (from Europe PMC, 2024-04-20)

Ranking

All databases:
4908/6000 (18.217%)
Genotype phenotype and variation:
694/852 (18.662%)
4908
Total Rank
6
Citations
0.6
z-index

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Record metadata

Created on: 2018-01-29
Curated by:
Mansoor Khan [2018-04-25]
Mansoor Khan [2018-04-12]
Qi Wang [2018-01-28]