Richard Mott is Weldon Professor of Computational and Statistical Genetics in the research department of Genetics, Evolution and Environment at University College London. He was previously at the Wellcome Centre for Human Genetics and a Professor by Research at Oxford University.

He has worked on physical mapping with Hans Lehrach at Imperial Cancer Research Fund laboratories in London, where he developed a suite of software tools for the construction and validation of physical maps [1] In 1995 he moved to the Sanger Centre to work on DNA sequence assembly where he wrote software that automatically analysed sequencing trace data in order to edit DNA sequence assemblies. This was used extensively to accelerate sequence production. He wrote the sequence CAFtools assembly pipeline [2] which was used for the pipeline assembly of the human and other genomes at Sanger, and developed software for spliced alignment of EST to genomic DNA.[3]

Between 1999 and 2015 he worked at the Wellcome Trust Centre for Human Genetics[4] where he served as Head of Bioinformatics and Statistical Genetics. In 2010 he stepped down to concentrate on his own research leading a group working on quantitative genetics in plants and mice. He moved to UCL in November 2015.

He has developed methods for mapping in an outbred stock of mice (the heterogeneous stock).[5] He developed the HAPPY software package [6] used for high-resolution QTL mapping which led to the identification of a quantitative trait gene underlying behavioral variation in mice.[7] As part of an international collaboration he is developing a genetic reference panel of recombinant inbred lines of mice, known as the Collaborative Cross. With Dr Paula Kover, Bath University, he has developed a genetic reference panel in Arabidopsis thaliana[8]

References

  1. ↑ Mott, R; Grigoriev, A; Maier, E; Hoheisel, J; Lehrach, H (1993). "Algorithms and software tools for ordering clone libraries: application to the mapping of the genome of Schizosaccharomyces pombe". Nucleic Acids Res. 21 (8): 1965–74. doi:10.1093/nar/21.8.1965. PMC 309439. PMID 8493107.
  2. ↑ Dear et al Genome Res. 1998, 8:260-7
  3. ↑ Mott, R (1997). "EST_GENOME: a program to align spliced DNA sequences to unspliced genomic DNA". Comput Appl Biosci. 13 (4): 477–8. doi:10.1093/bioinformatics/13.4.477. PMID 9283765.
  4. ↑ "The Wellcome Centre for Human Genetics — Wellcome Centre for Human Genetics".
  5. ↑ "Wellcome Trust Centre for Human Genetics - Heterogeneous Stock Mouse Resources". Archived from the original on 12 June 2013. Retrieved 2 May 2010.
  6. ↑ Mott et al Proc Natl Acad Sci U S A. 2000;97:12649-54
  7. ↑ Yalcin at al Nat Genet. 2004, 36:1197-202
  8. ↑ Kover et al PLoS Genet. 2009 Jul;5(7):e1000551
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