BBMAP paired-end alignment problem

[Mark]

Hi All

Trying to use bbmap to align some Illumina PE reads. My command line looks like this

bbmap.sh overwrite=t ref=A.fasta in=R1_001_val_1.100.fq in2=R2_001_val_2.100.fq minid=0.25 mappedonly=true out=out.sam  outu=unaligned_reads.fa maxindel=100000

When I do this out.sam contains alignments of only read1 though the log indicates that read2 reads were aligned

Read 1 data:            pct reads       num reads       pct bases          num bases

mapped:                 100.0000%             100       100.0000%              29779
unambiguous:            100.0000%             100       100.0000%              29779
ambiguous:                0.0000%               0         0.0000%                  0
low-Q discards:           0.0000%               0         0.0000%                  0

perfect best site:        0.0000%               0         0.0000%                  0
semiperfect site:        35.0000%              35        35.1758%              10475
rescued:                  0.0000%               0

Match Rate:                   NA               NA        88.8176%              26449
Error Rate:              65.0000%              65         4.4763%               1333
Sub Rate:                65.0000%              65         0.3627%                108
Del Rate:                 0.0000%               0         0.0000%                  0
Ins Rate:                49.0000%              49         4.1136%               1225
N Rate:                 100.0000%             100         6.7061%               1997


Read 2 data:            pct reads       num reads       pct bases          num bases

mapped:                 100.0000%             100       100.0000%              25636
unambiguous:            100.0000%             100       100.0000%              25636
ambiguous:                0.0000%               0         0.0000%                  0
low-Q discards:           0.0000%               0         0.0000%                  0

perfect best site:        0.0000%               0         0.0000%                  0
semiperfect site:        26.0000%              26        25.3745%               6505
rescued:                  2.0000%               2

Match Rate:                   NA               NA        86.8232%              22258
Error Rate:              74.0000%              74         4.9852%               1278
Sub Rate:                74.0000%              74         0.8894%                228
Del Rate:                 0.0000%               0         0.0000%                  0
Ins Rate:                42.0000%              42         4.0958%               1050
N Rate:                 100.0000%             100         8.1916%               2100

If I change the command line to

bbmap.sh overwrite=t ref=A.fasta in=R2_001_val_2.100.fq minid=0.25 mappedonly=true out=out.sam  outu=unaligned_reads.fa maxindel=100000

Read2 reads are indeed aligned.

Any thoughts what I'm doing wrong not to get paired end alignments with the first command line? I am using BBMap version 35.92.

Thanks

Mark