dbMTS
dbMTS is a comprehensive database of putative human microRNA target site (MTS) SNVs and their functional predictions. dbMTS collects all potential SNVs microRNA target seed regions in human 3’UTRs and provides their functional predictions and annotations to facilitate the steps of filtering and prioritizing SNVs from a huge list of all SNVs discovered in a whole exome sequencing (WES) study.
Description
More detailed information about this field from each metasource.
dbMTS is a comprehensive database of putative human microRNA target site (MTS) SNVs and their functional predictions. dbMTS collects all potential SNVs microRNA target seed regions in human 3’UTRs and provides their functional predictions and annotations to facilitate the steps of filtering and prioritizing SNVs from a huge list of all SNVs discovered in a whole exome sequencing (WES) study.
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:28:09.603111
Webpage:
http://database.liulab.science/dbMTSWebpage
More detailed information about this field from each metasource.
http://database.liulab.science/dbMTS
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:28:09.603111
Publications:
Publications
More detailed information about this field from each metasource.
dbMTS: A comprehensive database of putative human microRNA target site SNVs and their functional predictions
PMID: 32227657
metasource: bio.tools
version: extracted_at: 2022-11-04T11:28:09.603111
Publications
More detailed information about this field from each metasource.
dbMTS: A comprehensive database of putative human microRNA target site SNVs and their functional predictions
PMID: 32227657
metasource: bio.tools
version: extracted_at: 2022-11-04T11:28:09.603111
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dbMTS: A comprehensive database of putative human microRNA target site SNVs and their functional predictions
PubMed citations: 6.
6 articles citing: dbMTS: A comprehensive database of putative human microRNA target site SNVs and their functional predictions
dbNSFP v4: a comprehensive database of transcript-specific functional predictions and annotations for human nonsynonymous and splice-site SNVs. PMID:33261662
MobiDetails: online DNA variants interpretation. PMID:33161418
miRNASNP-v3: a comprehensive database for SNPs and disease-related variations in miRNAs and miRNA targets. PMID:32990748
Bioinformatics Analysis Revealed Novel 3'UTR Variants Associated with Intellectual Disability. PMID:32858868
Identification of MicroRNA-Related Tumorigenesis Variants and Genes in the Cancer Genome Atlas (TCGA) Data. PMID:32824926
The International Conference on Intelligent Biology and Medicine 2019 (ICIBM 2019): conference summary and innovations in genomics. PMID:31888451
Tags:
Tags
More detailed information about this field from each metasource.
functional, regulatory and non-coding rna
metasource: bio.tools
version: extracted_at: 2022-11-04T11:28:09.603111
gene transcripts
metasource: bio.tools
version: extracted_at: 2022-11-04T11:28:09.603111
exome sequencing
metasource: bio.tools
version: extracted_at: 2022-11-04T11:28:09.603111
genetic variation
metasource: bio.tools
version: extracted_at: 2022-11-04T11:28:09.603111
gene expression
metasource: bio.tools
version: extracted_at: 2022-11-04T11:28:09.603111
Tags
More detailed information about this field from each metasource.
functional, regulatory and non-coding rna
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:28:09.603111
gene transcripts
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:28:09.603111
exome sequencing
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:28:09.603111
genetic variation
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:28:09.603111
gene expression
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:28:09.603111
functional, regulatory and non-coding rna gene transcripts exome sequencing genetic variation gene expression
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