Open HenrikBengtsson opened 9 years ago
As a start:
> getFlagStat(bams[[1]])
description passed failed
1 in total (QC-passed reads + QC-failed reads) 100 0
2 duplicates 0 0
3 mapped (0.00%:-nan%) 0 0
4 paired in sequencing 0 0
5 read1 0 0
6 read2 0 0
7 properly paired (-nan%:-nan%) 0 0
8 with itself and mate mapped 0 0
9 singletons (-nan%:-nan%) 0 0
10 with mate mapped to a different chr 0 0
11 with mate mapped to a different chr (mapQ>=5) 0 0
BamDataFile should report on whether there are paired end reads or not in the file. Maybe there could also be both SE and PE reads?