Whole Genome Sequencing and RNA-Seq of a patient affected by CLL in order to identify structural variations (SVs) and chimeric transcripts, respectively.
High-throughput 3' DGE library preparation was conducted as per: dx.doi.org/10.17504/protocols.io.bumynu7w with 6 nucleotide barcodes on R2 for the 384 wells.Reads were demultiplexed using a cust
