I've aligned PacBio subreads (fasta) to a reference using Heng Li's BWA (the long read aligner - BWA-SW, using the command 'bwa bwasw'), and I'm trying to read these in using

> r = readAligned("test.bam", type="BAM")

Now, I know there's a potential problem here, in that BWA-SW will produce multiple lines with the same read id when it finds disconnected alignment blocks within reads (which should be the case for my data - transcript reads mapped to the genome). However, the resulting readAligned object:

> r
class: AlignedRead
length: 59664 reads; width: 126..12721 cycles
chromosome: NA NA ... NA NA
position: NA NA ... NA NA
strand: NA NA ... NA NA
alignQuality: NumericQuality
alignData varLabels: flag

has 59,664 reads, which is more than the number of unique read ids in the file, but fewer than the number of lines in the file. Furthermore, a test file containing 1 single alignment read in as so:

> r
class: AlignedRead
length: 0 reads; width:  cycles
chromosome:
position:
strand:
alignQuality: NumericQuality
alignData varLabels: flag

Can anybody suggest where I might have gone wrong?

session info:

> sessionInfo()
R version 2.14.1 (2011-12-22)
Platform: x86_64-redhat-linux-gnu (64-bit)

locale:
[1] C

attached base packages:
[1] stats     graphics  grDevices utils     datasets  methods   base     

other attached packages:
 [1] GenomicFeatures_1.6.9 AnnotationDbi_1.16.19 Biobase_2.14.0       
 [4] ShortRead_1.12.4      latticeExtra_0.6-19   RColorBrewer_1.0-5   
 [7] Rsamtools_1.6.3       lattice_0.20-6        Biostrings_2.22.0    
[10] GenomicRanges_1.6.7   IRanges_1.12.6       

loaded via a namespace (and not attached):
 [1] BSgenome_1.22.0    DBI_0.2-5          RCurl_1.91-1       RSQLite_0.11.1    
 [5] XML_3.9-4          biomaRt_2.10.0     bitops_1.0-4.1     grid_2.14.1       
 [9] hwriter_1.3        rtracklayer_1.14.4 tools_2.14.1       zlibbioc_1.0.1