1 Introduction

BamScale provides multithreaded sequential BAM traversal for R/Bioconductor workflows. The package is designed for users who already rely on Rsamtools, GenomicAlignments, and BiocParallel, but need faster BAM parsing without moving to a separate non-Bioconductor workflow model.

The package targets three common classes of BAM access:

metadata-oriented scans for filtering, fragment summaries, and quality control
generation of alignment objects for downstream GenomicAlignments workflows
sequence and quality extraction, including an optimized compact mode

The motivation for inclusion in Bioconductor is therefore straightforward: BamScale accelerates a core data-access bottleneck while preserving familiar Bioconductor inputs, filtering semantics, and output types.

2 Installation

At present, BamScale depends on the ompBAM engine and is intended for use with an OpenMP-capable toolchain.

if (!requireNamespace("BiocManager", quietly = TRUE)) {
    install.packages("BiocManager")
}

BiocManager::install("BamScale")

3 Basic usage

library(BamScale)

bam <- ompBAM::example_BAM("Unsorted")

3.1 Metadata-oriented BAM access

The most common BAM-access pattern is extraction of alignment metadata such as read name, flag, reference name, position, mapping quality, and CIGAR string.

x <- bam_read(
    file = bam,
    what = c("qname", "flag", "rname", "pos", "mapq", "cigar"),
    as = "data.frame",
    threads = 2
)

head(x)
#>                                       qname flag rname      pos mapq
#> 1  ST-E00600:137:H77Y3CCXY:1:1101:6837:1309  163    19   572614  255
#> 2  ST-E00600:137:H77Y3CCXY:1:1101:6837:1309   83    19   579499  255
#> 3 ST-E00600:137:H77Y3CCXY:1:1101:10450:1309  163     6 44252112  255
#> 4 ST-E00600:137:H77Y3CCXY:1:1101:10450:1309   83     6 44252124  255
#> 5 ST-E00600:137:H77Y3CCXY:1:1101:15077:1309   99    12 46185884  255
#> 6 ST-E00600:137:H77Y3CCXY:1:1101:15077:1309  147    12 46185968  255
#>           cigar
#> 1 1S88M6798N61M
#> 2      1S148M1S
#> 3      60S86M4S
#> 4      1S146M3S
#> 5        1S149M
#> 6      7S142M1S

3.2 Filtering with `ScanBamParam`

BamScale accepts Rsamtools::ScanBamParam, allowing existing filtering logic to be reused directly.

param <- Rsamtools::ScanBamParam(
    what = c("qname", "flag", "mapq"),
    mapqFilter = 20L,
    flag = Rsamtools::scanBamFlag(isUnmappedQuery = FALSE)
)

filtered <- bam_read(
    file = bam,
    param = param,
    as = "data.frame",
    threads = 2
)

head(filtered)
#>                                       qname flag mapq
#> 1  ST-E00600:137:H77Y3CCXY:1:1101:6837:1309  163  255
#> 2  ST-E00600:137:H77Y3CCXY:1:1101:6837:1309   83  255
#> 3 ST-E00600:137:H77Y3CCXY:1:1101:10450:1309  163  255
#> 4 ST-E00600:137:H77Y3CCXY:1:1101:10450:1309   83  255
#> 5 ST-E00600:137:H77Y3CCXY:1:1101:15077:1309   99  255
#> 6 ST-E00600:137:H77Y3CCXY:1:1101:15077:1309  147  255

3.3 Alignment-object output

When downstream workflows expect GenomicAlignments objects, bam_read() can return those directly.

ga <- bam_read(
    file = bam,
    what = c("qname", "flag", "rname", "pos", "cigar", "strand"),
    as = "GAlignments",
    threads = 2
)

ga
#> GAlignments object with 10000 alignments and 2 metadata columns:
#>           seqnames strand              cigar    qwidth     start       end
#>              <Rle>  <Rle>        <character> <integer> <integer> <integer>
#>       [1]       19      +      1S88M6798N61M       150    572614    579560
#>       [2]       19      -           1S148M1S       150    579499    579646
#>       [3]        6      +           60S86M4S       150  44252112  44252197
#>       [4]        6      -           1S146M3S       150  44252124  44252269
#>       [5]       12      +             1S149M       150  46185884  46186032
#>       ...      ...    ...                ...       ...       ...       ...
#>    [9996]        2      -         16S122M12S       150 186680457 186680578
#>    [9997]       15      +           4S143M3S       150  90501177  90501319
#>    [9998]       15      -        26M2I56M66S       150  90501301  90501382
#>    [9999]        4      + 3M336N95M752N51M1S       150 121801488 121802724
#>   [10000]        4      -      1S117M121N32M       150 121802677 121802946
#>               width     njunc |                  qname      flag
#>           <integer> <integer> |            <character> <integer>
#>       [1]      6947         1 | ST-E00600:137:H77Y3C..       163
#>       [2]       148         0 | ST-E00600:137:H77Y3C..        83
#>       [3]        86         0 | ST-E00600:137:H77Y3C..       163
#>       [4]       146         0 | ST-E00600:137:H77Y3C..        83
#>       [5]       149         0 | ST-E00600:137:H77Y3C..        99
#>       ...       ...       ... .                    ...       ...
#>    [9996]       122         0 | ST-E00600:137:H77Y3C..        83
#>    [9997]       143         0 | ST-E00600:137:H77Y3C..       163
#>    [9998]        82         0 | ST-E00600:137:H77Y3C..        83
#>    [9999]      1237         2 | ST-E00600:137:H77Y3C..       163
#>   [10000]       270         1 | ST-E00600:137:H77Y3C..        83
#>   -------
#>   seqinfo: 25 sequences from an unspecified genome; no seqlengths

3.4 Sequence and quality extraction

For seq and qual, BamScale supports both a compatibility-preserving mode and an optimized compact mode.

seqqual_compatible <- bam_read(
    file = bam,
    what = c("qname", "seq", "qual"),
    as = "data.frame",
    seqqual_mode = "compatible",
    threads = 2
)

head(seqqual_compatible)
#>                                       qname
#> 1  ST-E00600:137:H77Y3CCXY:1:1101:6837:1309
#> 2  ST-E00600:137:H77Y3CCXY:1:1101:6837:1309
#> 3 ST-E00600:137:H77Y3CCXY:1:1101:10450:1309
#> 4 ST-E00600:137:H77Y3CCXY:1:1101:10450:1309
#> 5 ST-E00600:137:H77Y3CCXY:1:1101:15077:1309
#> 6 ST-E00600:137:H77Y3CCXY:1:1101:15077:1309
#>                                                                                                                                                      seq
#> 1 NGACCGGCGAGGAATAGGAATCATGGCGGCTGCGCTGTTCGTGCTGCTGGGATTCGCGCTGCTGGGCACCCACGGAGCCTCCGGGGCTGCCGGCACAGTCTTCACTACCGTAGAAGACCTTGGCTCGAAGATACTCCTCACCTGCTCCTT
#> 2 TGCCGGCACAGTCTTCACTACCGTAGAAGACCTTGGCTCCAAGATACTCCTCACCTGCTCCTTGAATGACAGCGCCACAGAGGTCACAGGGCACCGCTGGCTGAAGGCGGGCGTGGTGCTGAAGGAGGACGCGCTGCCAGGCCAGAAAAN
#> 3 NGGAGCTTCGAGGTGGTATATATGACCGAGCCCATTAATGAGTACTGTGTGCAGCAGCGTAAGCAATTTGATGGGAAGAGCGTGGTCTCAGTTAGCAAGGAGGGTCTGGAGCTGCCTGAGGATGAGGAGGAGCTGAAGAAGATGGAGGAG
#> 4 TGGGAAGAGCCTGGTCTCAGTTACCAAGGAGGGTCTGGAGCTGCCTGAGGATGAGTAGGAGAAGAAGAAGATGGAAGAGAGCAAGGTAAAGTTTGAGAACCTCTGCAAGCTCATGAAAGAAATCTTAGATAAGAAGGTCGAGATGGTGAN
#> 5 NGCATCTCTACCCCTACTGTCCAGTAGGTGGGATGTGGCTGGGCTGGACAGTCCAGATTATACGAACTGGCAACTCTGAACAAACACCCTCCCTGGAAACAATATTATATTTGATGGTTAGATTCTTTAGCAAACCTATTACATTATTCG
#> 6 AACAAAAACCCTCCCTAGCAACAATATTATATTTGATCGTTAGATTCTTTAGCAAACCTATTACCTTATTCGATGTCAGCTAACCTCTTGGTTTGATCATCTTTTCCAGCTGCTCTAGGGGCCTAACCACCTTGGATAACCTGGTCTCTN
#>                                                                                                                                                     qual
#> 1 #AA-AAFJFJJJJJJJJJAAJJJJJJJJJJJJJF<-FJF-AAFJJJJFFJJFFF<FFJ-<<AFAFF7-AFJFJJJJJ77FJAAJJ7AA777AJJAJFJ-A<AA<AAF7FFA-FAFA<-77<FJA--)77A7AA7--7AF<)7777<))--
#> 2 -FAAA)-AJFF7JJFFAF-FJAF-<A-7--JJJFA-F-A7-<-F7-FFJFFJAFJFJJAJFJ<FFJJJFAF7JJFFJFFJ7<-<AA-<AF-JJA<7<777A7<JA77-7JJJJJFJJJFJJJFFJJFJJJJJJJJJF7-JJJF-AFAAA#
#> 3 #AA-AFFJFJJAAFFJAJJJ<AJJJFJJJJJA<<F7-F-<-<FFAFFJFAJJF<<FJ----<<-7<J-FF-AJJJF<J<JF-AFAA7-7AJJJF-7777A-7AA---777---7FJ--AFA7-7AAJFAA)7))7---A<7<--7---A7
#> 4 AJA-FFJJJFF<7FF-AA<7F<AF<-7FJFJJJJJFF-<7-JFJJJJFFAJFJ<A-JF-JJJAFFFFJJJJFJ7<--F-A-<7JF<-FF<<---<-77<-A-FJJFJJFJFJJJJJJJJJJJ<JJJJJJJJJJJJJJ<7JJJF<FFAAA#
#> 5 #AAFFF-FJJJA-AFJJJJJJJJJJJJJJJJJJJJJJJJFJF7-7FJJJFJJJ<<F-FF-FJJFJFJ-F<JA7-7-7AF-JJJFJJJFJJJ7FJJJ<FJJJJJJJJJJJJFJJJJJ7FFJ-7-7-A-AFFF-F--7F7AJJJJJ-<<FJJ
#> 6 7A7-7--<A-)<)AA7-7-A<<7-FF<7<F<7-7A-F-JJAAFJJJJJJA<JF<A7JJJFAA-J<JJFJJA-7<JJJJFFJJAJJA7<<<7<FJJAJJJFJJFJJJA-JJFJJFJJJJJJJJFJJJJJJ<F-JJJJJFFJJFJJFFAAA#

Compact mode returns lower-level raw vectors for throughput-oriented workflows. These values can be decoded back to ordinary strings explicitly when needed.

seqqual_compact <- bam_read(
    file = bam,
    what = c("qname", "qwidth", "seq", "qual"),
    as = "data.frame",
    seqqual_mode = "compact",
    threads = 2
)

head(seqqual_compact)
#>                                       qname qwidth          seq         qual
#> 1  ST-E00600:137:H77Y3CCXY:1:1101:6837:1309    150 f4, 12, .... 02, 20, ....
#> 2  ST-E00600:137:H77Y3CCXY:1:1101:6837:1309    150 84, 22, .... 0c, 25, ....
#> 3 ST-E00600:137:H77Y3CCXY:1:1101:10450:1309    150 f4, 41, .... 02, 20, ....
#> 4 ST-E00600:137:H77Y3CCXY:1:1101:10450:1309    150 84, 44, .... 20, 29, ....
#> 5 ST-E00600:137:H77Y3CCXY:1:1101:15077:1309    150 f4, 21, .... 02, 20, ....
#> 6 ST-E00600:137:H77Y3CCXY:1:1101:15077:1309    150 11, 21, .... 16, 20, ....

seqqual_decoded <- decode_seqqual_compact(seqqual_compact)
head(seqqual_decoded)
#>                                       qname qwidth
#> 1  ST-E00600:137:H77Y3CCXY:1:1101:6837:1309    150
#> 2  ST-E00600:137:H77Y3CCXY:1:1101:6837:1309    150
#> 3 ST-E00600:137:H77Y3CCXY:1:1101:10450:1309    150
#> 4 ST-E00600:137:H77Y3CCXY:1:1101:10450:1309    150
#> 5 ST-E00600:137:H77Y3CCXY:1:1101:15077:1309    150
#> 6 ST-E00600:137:H77Y3CCXY:1:1101:15077:1309    150
#>                                                                                                                                                      seq
#> 1 NGACCGGCGAGGAATAGGAATCATGGCGGCTGCGCTGTTCGTGCTGCTGGGATTCGCGCTGCTGGGCACCCACGGAGCCTCCGGGGCTGCCGGCACAGTCTTCACTACCGTAGAAGACCTTGGCTCGAAGATACTCCTCACCTGCTCCTT
#> 2 TGCCGGCACAGTCTTCACTACCGTAGAAGACCTTGGCTCCAAGATACTCCTCACCTGCTCCTTGAATGACAGCGCCACAGAGGTCACAGGGCACCGCTGGCTGAAGGCGGGCGTGGTGCTGAAGGAGGACGCGCTGCCAGGCCAGAAAAN
#> 3 NGGAGCTTCGAGGTGGTATATATGACCGAGCCCATTAATGAGTACTGTGTGCAGCAGCGTAAGCAATTTGATGGGAAGAGCGTGGTCTCAGTTAGCAAGGAGGGTCTGGAGCTGCCTGAGGATGAGGAGGAGCTGAAGAAGATGGAGGAG
#> 4 TGGGAAGAGCCTGGTCTCAGTTACCAAGGAGGGTCTGGAGCTGCCTGAGGATGAGTAGGAGAAGAAGAAGATGGAAGAGAGCAAGGTAAAGTTTGAGAACCTCTGCAAGCTCATGAAAGAAATCTTAGATAAGAAGGTCGAGATGGTGAN
#> 5 NGCATCTCTACCCCTACTGTCCAGTAGGTGGGATGTGGCTGGGCTGGACAGTCCAGATTATACGAACTGGCAACTCTGAACAAACACCCTCCCTGGAAACAATATTATATTTGATGGTTAGATTCTTTAGCAAACCTATTACATTATTCG
#> 6 AACAAAAACCCTCCCTAGCAACAATATTATATTTGATCGTTAGATTCTTTAGCAAACCTATTACCTTATTCGATGTCAGCTAACCTCTTGGTTTGATCATCTTTTCCAGCTGCTCTAGGGGCCTAACCACCTTGGATAACCTGGTCTCTN
#>                                                                                                                                                     qual
#> 1 #AA-AAFJFJJJJJJJJJAAJJJJJJJJJJJJJF<-FJF-AAFJJJJFFJJFFF<FFJ-<<AFAFF7-AFJFJJJJJ77FJAAJJ7AA777AJJAJFJ-A<AA<AAF7FFA-FAFA<-77<FJA--)77A7AA7--7AF<)7777<))--
#> 2 -FAAA)-AJFF7JJFFAF-FJAF-<A-7--JJJFA-F-A7-<-F7-FFJFFJAFJFJJAJFJ<FFJJJFAF7JJFFJFFJ7<-<AA-<AF-JJA<7<777A7<JA77-7JJJJJFJJJFJJJFFJJFJJJJJJJJJF7-JJJF-AFAAA#
#> 3 #AA-AFFJFJJAAFFJAJJJ<AJJJFJJJJJA<<F7-F-<-<FFAFFJFAJJF<<FJ----<<-7<J-FF-AJJJF<J<JF-AFAA7-7AJJJF-7777A-7AA---777---7FJ--AFA7-7AAJFAA)7))7---A<7<--7---A7
#> 4 AJA-FFJJJFF<7FF-AA<7F<AF<-7FJFJJJJJFF-<7-JFJJJJFFAJFJ<A-JF-JJJAFFFFJJJJFJ7<--F-A-<7JF<-FF<<---<-77<-A-FJJFJJFJFJJJJJJJJJJJ<JJJJJJJJJJJJJJ<7JJJF<FFAAA#
#> 5 #AAFFF-FJJJA-AFJJJJJJJJJJJJJJJJJJJJJJJJFJF7-7FJJJFJJJ<<F-FF-FJJFJFJ-F<JA7-7-7AF-JJJFJJJFJJJ7FJJJ<FJJJJJJJJJJJJFJJJJJ7FFJ-7-7-A-AFFF-F--7F7AJJJJJ-<<FJJ
#> 6 7A7-7--<A-)<)AA7-7-A<<7-FF<7<F<7-7A-F-JJAAFJJJJJJA<JF<A7JJJFAA-J<JJFJJA-7<JJJJFFJJAJJA7<<<7<FJJAJJJFJJFJJJA-JJFJJFJJJJJJJJFJJJJJJ<F-JJJJJFFJJFJJFFAAA#

3.5 Fast count summaries

bam_count() provides chromosome-level count summaries using the same BAM filtering model.

counts <- bam_count(bam, threads = 2)
counts
#>    seqname seqlength count
#> 1        1 248956422  1308
#> 2       10 133797422   308
#> 3       11 135086622   600
#> 4       12 133275309   648
#> 5       13 114364328   162
#> 6       14 107043718   230
#> 7       15 101991189   294
#> 8       16  90338345   334
#> 9       17  83257441   570
#> 10      18  80373285    78
#> 11      19  58617616   600
#> 12       2 242193529   586
#> 13      20  64444167   168
#> 14      21  46709983    76
#> 15      22  50818468   200
#> 16       3 198295559   454
#> 17       4 190214555   252
#> 18       5 181538259   516
#> 19       6 170805979   824
#> 20       7 159345973   412
#> 21       8 145138636   452
#> 22       9 138394717   372
#> 23      MT     16569   288
#> 24       X 156040895   254
#> 25       Y  57227415    14
#> 26       *        NA     0

4 Relationship to existing Bioconductor tools

BamScale is intended to complement, not replace, existing Bioconductor packages.

Rsamtools remains the canonical low-level BAM access layer in R and defines the filtering idioms that BamScale reuses through ScanBamParam.
GenomicAlignments remains the standard package for alignment-centric downstream workflows, and BamScale supports direct generation of compatible alignment objects.
BiocParallel remains the standard mechanism for file-level parallelism, and BamScale adds a second axis of parallelism through per-file OpenMP threads.

The main difference is therefore performance-oriented: BamScale accelerates the traversal step itself while staying close to existing Bioconductor usage patterns.

5 Session information

sessionInfo()
#> R version 4.6.0 RC (2026-04-17 r89917)
#> Platform: x86_64-pc-linux-gnu
#> Running under: Ubuntu 24.04.4 LTS
#> 
#> Matrix products: default
#> BLAS:   /home/biocbuild/bbs-3.23-bioc/R/lib/libRblas.so 
#> LAPACK: /usr/lib/x86_64-linux-gnu/lapack/liblapack.so.3.12.0  LAPACK version 3.12.0
#> 
#> locale:
#>  [1] LC_CTYPE=en_US.UTF-8       LC_NUMERIC=C              
#>  [3] LC_TIME=en_GB              LC_COLLATE=C              
#>  [5] LC_MONETARY=en_US.UTF-8    LC_MESSAGES=en_US.UTF-8   
#>  [7] LC_PAPER=en_US.UTF-8       LC_NAME=C                 
#>  [9] LC_ADDRESS=C               LC_TELEPHONE=C            
#> [11] LC_MEASUREMENT=en_US.UTF-8 LC_IDENTIFICATION=C       
#> 
#> time zone: America/New_York
#> tzcode source: system (glibc)
#> 
#> attached base packages:
#> [1] stats     graphics  grDevices utils     datasets  methods   base     
#> 
#> other attached packages:
#> [1] BamScale_0.99.9  BiocStyle_2.40.0
#> 
#> loaded via a namespace (and not attached):
#>  [1] Matrix_1.7-5                jsonlite_2.0.0             
#>  [3] compiler_4.6.0              BiocManager_1.30.27        
#>  [5] crayon_1.5.3                Rcpp_1.1.1-1.1             
#>  [7] SummarizedExperiment_1.42.0 Biobase_2.72.0             
#>  [9] Rsamtools_2.28.0            GenomicRanges_1.64.0       
#> [11] bitops_1.0-9                Biostrings_2.80.0          
#> [13] GenomicAlignments_1.48.0    parallel_4.6.0             
#> [15] jquerylib_0.1.4             IRanges_2.46.0             
#> [17] Seqinfo_1.2.0               BiocParallel_1.46.0        
#> [19] yaml_2.3.12                 fastmap_1.2.0              
#> [21] lattice_0.22-9              R6_2.6.1                   
#> [23] XVector_0.52.0              S4Arrays_1.12.0            
#> [25] generics_0.1.4              knitr_1.51                 
#> [27] BiocGenerics_0.58.0         DelayedArray_0.38.1        
#> [29] bookdown_0.46               MatrixGenerics_1.24.0      
#> [31] bslib_0.10.0                rlang_1.2.0                
#> [33] cachem_1.1.0                ompBAM_1.16.0              
#> [35] xfun_0.57                   sass_0.4.10                
#> [37] otel_0.2.0                  SparseArray_1.12.2         
#> [39] cli_3.6.6                   grid_4.6.0                 
#> [41] digest_0.6.39               lifecycle_1.0.5            
#> [43] S4Vectors_0.50.0            evaluate_1.0.5             
#> [45] cigarillo_1.2.0             codetools_0.2-20           
#> [47] abind_1.4-8                 stats4_4.6.0               
#> [49] rmarkdown_2.31              matrixStats_1.5.0          
#> [51] tools_4.6.0                 htmltools_0.5.9

Getting started with BamScale

4 May 2026

Contents

1 Introduction

2 Installation

3 Basic usage

3.1 Metadata-oriented BAM access

3.2 Filtering with `ScanBamParam`

3.3 Alignment-object output

3.4 Sequence and quality extraction

3.5 Fast count summaries

4 Relationship to existing Bioconductor tools

5 Session information

Getting started with BamScale

4 May 2026

Contents

1 Introduction

2 Installation

3 Basic usage

3.1 Metadata-oriented BAM access

3.2 Filtering with ScanBamParam

3.3 Alignment-object output

3.4 Sequence and quality extraction

3.5 Fast count summaries

4 Relationship to existing Bioconductor tools

5 Session information

3.2 Filtering with `ScanBamParam`