Enrichment for Cancer research

[kant1_IC]

Dear all,

we planed to use NGS technologies in order to find mutations in samples coming form patient suffereing of various cancer. We have focused more on enrichment strategies (capture or amplicon) to facilitate the the sequence analysis.
Is anyone already used this kind of strategies and if yes which one ??

Thanks in advance


kant1

[adaptivegenome]

Look up The Cancer Genome Atlas (TCGA).