Chimeras

• Alignment for each sample against merged genomes, with STARsolo: arrayRunSTARSolo.sh.

  This script calls runSTARSolo.sh for each sample.

  It requires some preprocessing generating the genome index (genome_index.sh) and lists of fastq files to process (generate_fastq_lists.sh).

  The genomes were download already merged from 10x.

• Classify cell barcodes by specie, separate_barcodes.R

TODO

• Filter the fastq files, separating the reads according by the classification of their barcode (human or mouse)(in process, filter_fastqs.sh)

• Realign the human and mouse fastq files with their respective genome, so all reads from a same cell are uniformly aligned to the same genome.