The Cancer Sequencing Service
supports whole genome sequencing and data delivery for genome pairs and genome trios.
The Standard Sequencing Service
supports whole genome sequencing and data delivery for individual genomes.
Not exact matches
This time Venter turned to Diamandis (Page had introduced them) not because of a failure at the NIH but because financiers weren't
supporting companies that did
whole -
genome sequencing.
This time Venter turned to Diamandis (Page had introduced them) not because of a failure at the NIH but because financiers weren't
supporting companies that did
whole -
genome sequencing.
This paper
supports the advantages of the use of
whole genome sequencing to search for mutations in patients with RP.
As a part of SciLifeLab's ambition to
support and collaborate with governmental authorities SciLifeLab has, together with the National Veterinary Institute and the National Food Agency, organized a workshop on subtyping of pathogenic microorganisms using
whole -
genome sequencing.
Because current typing methods often fail to resolve the infection source in possible nosocomial cases, we aimed to determine whether
whole -
genome sequencing (WGS) could be used to
support or refute suspected links between cases and hospitals.
An integrated computational pipeline and database to
support whole -
genome sequence annotation C.J. Mungall, S. Misra, B.P. Berman, J. Carlson, E. Frise, N. Harris, B. Marshall, S. Shu, J.S. Kaminker, S.E. Prochnik, C.D. Smith, E. Smith, J.L. Tupy, C. Wiel, G.M. Rubin and S.E. Lewis Genome Biology (2002) 3 (12): research0081.1 - 0081.11 Download entire paper in pdf
genome sequence annotation C.J. Mungall, S. Misra, B.P. Berman, J. Carlson, E. Frise, N. Harris, B. Marshall, S. Shu, J.S. Kaminker, S.E. Prochnik, C.D. Smith, E. Smith, J.L. Tupy, C. Wiel, G.M. Rubin and S.E. Lewis
Genome Biology (2002) 3 (12): research0081.1 - 0081.11 Download entire paper in pdf
Genome Biology (2002) 3 (12): research0081.1 - 0081.11 Download entire paper in pdf format
The new article, yet to be peer - reviewed or published, concludes, «Taken together, these
whole -
genome -
sequencing - level results
support the idea that in specific cases, CRISPR - Cas9 editing can precisely edit the
genome at the organismal level and may not introduce numerous, unintended, off - target mutations.»
Professor George Patrinos (University of Patras, Greece) gave an update on the use of
whole genome sequencing in pharmacogenomics, which followed by several company lectures that
supported the event as sponsors.
October 1, 2014 PRA Research Update The University of Missouri has used
support from the TTHWF to generate separate
whole genome sequences from two different Tibetan Terriers with PRA, one with a relatively early onset and the other with a later onset.
Funding from the Portuguese Water Dog Club of America (PWDCA) provided major
support for the research in its initial phase and the Portuguese Water Dog Foundation funded the
whole genome sequencing steps that were critical to the mutation's discovery.