The Wheeler lab has been awarded an NIH R15 grant from the National Institute of General Medical Sciences to develop “Improved protein-DNA models for translated sequence search with profile Hidden Markov models”. The grant is for $426K over three years, beginning April 1, 2017.
Fast and sensitive sequence database search is fundamental to modern molecular biology. The funded research will improve the accuracy of annotation of protein-coding content in sequenced genomes and metagenomic datasets. The research builds on established sequence database search software that employs probabilistic models to increase sensitivity through greater statistical power and ability to better model family complexity. The probabilistic models are called profile hidden Markov models (profile HMMs), and the software is HMMER.
Dr. Wheeler’s group will develop new models that account for frameshifting mutations or errors that obscure the protein-coding nature of sequence, and for splice sites that break genes or domains into distant fragments on the genome. Through a combination of new algorithms and application of existing approaches, these models will be fast enough to use for large-scale annotation, such as in the EMBL European Bioinformatics Institute’s Metagenomics Portal.
(See the press release: here)
I’m proud to be a signatory on a guest column in today’s Missoulian, which highlights the terrific educational atmosphere and excellent research found on the University of Montana campus. Despite trying financial times resulting from an enrollment drop caused by multiple complex factors, this University is home to a great many tremendous educators and researchers.
The Wheeler lab has been awarded competitive pilot project funding through the University of Montana Center for Biomolecular Structure and Dynamics (CBSD). The grant will support early development of methods for reducing false sequence annotation of large genomic DNA datasets due to repetitive sequence and alignment overextension, and will fund two students in our group for the next year. CBSD is supported by a National Institutes of General Medical Science (NIH NIGMS) IdeA program Center of Biomolecular Research Excellence (CoBRE) Phase II grant.
Congratulations to lab member Gilia Patterson, who today was recognized as the University of Montana Outstanding Senior in Genetics and Evolution. Gilia has done great work with me on understanding sources of transposable element mis-classification (manuscript coming soon to a theatre near you), and we’re happy as can be for her!
Dfam is growing up. This is the first major expansion of the database since it’s inception. We’ve added repeat families from four new organisms: mouse, zebrafish, fruit fly, and nematode. In total, this release includes 2,844 new familes ( 4,150 total ).
I’m wrapping up a lengthy trip to England and Ireland, in which I had the chance to catch up with a member of the lab, Rutger Evans, who has been working on a summer project at the EBI, under the guidance of one of my favorite collaborators, Rob Finn.
Alex Nord has just been awarded a Center for Biomolecular Structure and Dynamics Graduate Student Fellowship for the summer of 2016. The fellowship will support Alex while he continues research on using spaced seeds to boost both speed and sensitivity in the context of database search with profile hidden Markov models (in HMMER, of course).
Read more at: http://news.umt.edu/2015/06/060915cbsd.php