4.8 Article

HmtDB, a genomic resource for mitochondrion-based human variability studies

Journal

NUCLEIC ACIDS RESEARCH
Volume 40, Issue D1, Pages D1150-D1159

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/nar/gkr1086

Keywords

-

Funding

  1. 'Fondo di Ateneo' (University of Bari)
  2. Fondazione della Cassa di Risparmio di Puglia
  3. Italian Ministry of University and Research (MIUR) [J31J10000040001]
  4. Fondo FIRB

Ask authors/readers for more resources

HmtDB (>http://www.hmtdb.uniba.it:8080/hmdb) is a open resource created to support population genetics and mitochondrial disease studies. The database hosts human mitochondrial genome sequences annotated with population and variability data, the latter being estimated through the application of the SiteVar software based on site-specific nucleotide and amino acid variability calculations. The annotations are manually curated thus adding value to the quality of the information provided to the end-user. Classifier tools implemented in HmtDB allow the prediction of the haplogroup for any human mitochondrial genome currently stored in HmtDB or externally submitted de novo by an end-user. Haplogroup definition is based on the Phylotree system. End-users accessing HmtDB are hence allowed to (i) browse the database through the use of a multi-criterion 'query' system; (ii) analyze their own human mitochondrial sequences via the 'classify' tool (for complete genomes) or by downloading the 'fragment-classifier' tool (for partial sequences); (iii) download multi-alignments with reference genomes as well as variability data.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.8
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available