Highlights of Relevant Experience: Managed matrix team of U.S. and U.K. scientists in first ever large - scale use of US DNA TAP Store integrated liquid handling capabilities to
support deep sequencing technology project to generate data for genetic rare variants and for potential asset realignment with project delivery of more than 12,000 samples prepared under extremely tight time lines for GlaxoSmithKline.
Not exact matches
To find a solution to this, Marcel Martin at Bioinformatics Long - term
Support (WABI) at SciLifeLab, in collaboration with the group of Gunilla Karlsson Hedestam at Karolinska Institutet, has developed a practical, computational technique, IgDiscover, that enables rapid production of individualized V gene databases following
deep sequencing of expressed antibody repertoires.
Taken together, these results
support the utility of VarScan for variant detection in next - gen
sequencing, and demonstrate the feasibility of large - scale mutational profiling by
deep resequencing of pooled samples.