Prepar fastq files at a given barcode.
.singlePrepUMI4C( fq_R1, fq_R2, bait_seq, bait_pad, res_enz, prep_dir, numb_reads = 1e+09 )
| fq_R1 | Fastq file R1. |
|---|---|
| fq_R2 | Fastq file R2. |
| bait_seq | Character containing the bait primer sequence. |
| bait_pad | Character containing the pad sequence (sequence between the bait primer and the restriction enzyme sequence). |
| res_enz | Character containing the restriction enzyme sequence. |
| prep_dir | Prep directory. |
| numb_reads | Number of lines from the FastQ file to load in each loop. If having memory size problems, change it to a smaller number. Default=1e9. |
Creates a compressed FASTQ file in wk_dir/prep named
basename(Fastq)).fq.gz, containing the filtered reads with the UMI
sequence in the header. A data.frame object with the statisitics is also
returned.