dbDNV
The duplicated gene nucleotide variants database (dbDNV) (http://goods.ibms.sinica.edu.tw/DNVs/) promotes accurate variation annotation. Aside from the flat file download, users can explore the gene-related duplications and the associated DNVs by DGL and DNV searches, respectively. In addition, the dbDNV contains 304,110 DNV-coupled SNPs. From DNV-coupled SNP search, users observe which SNP records are also variants among duplicates.
Description
More detailed information about this field from each metasource.
The duplicated gene nucleotide variants database (dbDNV) (http://goods.ibms.sinica.edu.tw/DNVs/) promotes accurate variation annotation. Aside from the flat file download, users can explore the gene-related duplications and the associated DNVs by DGL and DNV searches, respectively. In addition, the dbDNV contains 304,110 DNV-coupled SNPs. From DNV-coupled SNP search, users observe which SNP records are also variants among duplicates.
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:34:24.530771
Webpage:
http://goods.ibms.sinica.edu.tw/DNVs/Webpage
More detailed information about this field from each metasource.
http://goods.ibms.sinica.edu.tw/DNVs/
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:34:24.530771
Publications:
Publications
More detailed information about this field from each metasource.
dbDNV: a resource of duplicated gene nucleotide variants in human genome
PMID: 21097891
metasource: bio.tools
version: extracted_at: 2022-11-04T11:34:24.530771
Publications
More detailed information about this field from each metasource.
dbDNV: a resource of duplicated gene nucleotide variants in human genome
PMID: 21097891
metasource: bio.tools
version: extracted_at: 2022-11-04T11:34:24.530771
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dbDNV: a resource of duplicated gene nucleotide variants in human genome
PubMed citations: 9.
9 articles citing: dbDNV: a resource of duplicated gene nucleotide variants in human genome
eDiVA-Classification and prioritization of pathogenic variants for clinical diagnostics. PMID:31026367
Small Segmental Duplications in Drosophila-High Rate of Emergence and Elimination. PMID:30689862
Perspective: DNA Copy Number Variations in Cardiovascular Diseases. PMID:30560231
Reverse Transcription Errors and RNA-DNA Differences at Short Tandem Repeats. PMID:27413049
VarBin, a novel method for classifying true and false positive variants in NGS data. PMID:24266885
RNA-Seq approach for genetic improvement of meat quality in pig and evolutionary insight into the substrate specificity of animal carbonyl reductases. PMID:22962580
Genomic position mapping discrepancies of commercial SNP chips. PMID:22363540
Genome-wide signatures of 'rearrangement hotspots' within segmental duplications in humans. PMID:22194928
Clusters of nucleotide substitutions and insertion/deletion mutations are associated with repeat sequences. PMID:21697975
Tags:
Tags
More detailed information about this field from each metasource.
dna polymorphism
metasource: bio.tools
version: extracted_at: 2022-11-04T11:34:24.530771
genetic variation
metasource: bio.tools
version: extracted_at: 2022-11-04T11:34:24.530771
transcription factors and regulatory sites
metasource: bio.tools
version: extracted_at: 2022-11-04T11:34:24.530771
gene transcripts
metasource: bio.tools
version: extracted_at: 2022-11-04T11:34:24.530771
Tags
More detailed information about this field from each metasource.
dna polymorphism
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:34:24.530771
genetic variation
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:34:24.530771
transcription factors and regulatory sites
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:34:24.530771
gene transcripts
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:34:24.530771
dna polymorphism genetic variation transcription factors and regulatory sites gene transcripts
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