pileup-events

Count alleles and alignment events per position for a specified genomic region.

Installation

Minimal

You will need cmake>=3.16 and htslib>=1.14 installed, and preferably pkg-config if you want to install the easy way. If you want to create python and/or R bindings you will also need SWIG>=4.0. If you don't already have these dependencies, it would be best to install via your package manager. e.g. on Ubuntu

  apt install cmake swig pkg-config libhts-dev

or on mac

  brew install cmake swig pkg-config htslib

Once you have these dependencies, to create the pileup-events binary and/or R and python bindings:

  # git clone <this repo>
  # cd <repo folder>
  mkdir build
  cd build
  cmake .. \
    -DMAKE_EXE=ON \ # create binary
    -DMAKE_PY_BINDS=ON \ # make python bindings
    -DMAKE_R_BINDS=ON # R
  cmake --build .

You can then invoke the binary like ./path/to/pileup-events --help. Add the binary path to PATH to be able to call pileup-events from anywhere. For usage of the R and python bindings see subsequent sections.

Extended

It is possible to direct cmake to use specific builds of htslib via the -DHTS_INCLUDE_DIR and -DHTS_LIBRARY options to cmake ...

pileup-events relies on cxxopts for the CLI interface, and Catch2 if building the test binary. These dependencies will be fetched automatically during the build process.

Usage

pileup-events --help:

-----pileup-events:-------------------------------------|
                                                        |
  Count alleles and alignment events per position for   |
  a specified genomic region.                           |
                                                        |
   -----------                                          |
                                                        |
  Where reference names contain colons, surround in     |
  curly braces like {HLA-DRB1*12:17}:<start>{-<end>}.   |
                                                        |
  chr1:100 is treated as the single base pair region    |
  chr1:100-100. chr1:-100 is shorthand for chr1:1-100   |
  and chr1:100- is ch1:100-<end>. All co-ordinates are  |
  1-based, end-inclusive; i.e. as reported in a VCF.    |
                                                        |
  A result matrix with end-start rows and 22 columns    |
  of event counters (see --head) is printed to stdout   |
  as a csv. The first 12 columns represent events on    |
  the forward strand, the next 12 the reverse.          |
                                                        |
--------------------------------------------------------|

Usage:
  pileup-events [OPTION...] <.BAM/.CRAM> chr:start-end

  -b, --baseq arg         Minimum base quality to treat base as
                          unambiguous. (default 30)
  -m, --mapq arg          Minimum mapping quality to include read (default
                          25)
  -c, --clip arg          Treat bases within <clip> bases of read edges as
                          ambiguous. (default 0)
  -i, --include arg       Include only reads with all bits set in sam flag.
                          Provide flag as integer. (default 0)
  -e, --exclude arg       Exclude reads with any bits set in sam flag.
                          Provide flag as integer. (default 3844)
  -d, --depth arg         Maximum read depth (default 1000000)
      --head              Print header
      --row               Print genomic position index for each row
      --discard-overlaps  Avoid double counting of bases from the same
                          template
  -h, --help              Print usage
      --version           Print program version

Pick a location to investigate, for example a variant from a VCF or a region from a BED file, and run on that location to see the event counts.

e.g.:

  pileup-events \
    -i 2 \  # only count reads in proper pairs
    ~/path/to/sample.bam \
    chr1:1000  # single location

  pileup-events \
    ~/path/to/sample.bam \
    chr1:1000-2000  # 1001bp range

The region string is 1-indexed, end-inclusive, i.e. identical to samtools view - excepting the fact that pileup-events allows a series of shorthands such as <chr>:<pos> for a single location. See the helptext for more details. Assuming compilation against a recent version of htslib, both .bam and .cram are in principle supported. No testing on cram has been done as of yet.

R & Python Bindings

Bindings for usage of pileup events in both R and Python can be generated during compilation. This is enabled by SWIG. As described in the installation section above, python bindings may be created with the -DMAKE_PY_BINDS=ON option and R with -DMAKE_R_BINDS=ON. Doing so will result in the generation of build/python and build/r respectively.

At present bindings are somewhat rudimentary - this may be improved upon in the future. Usage is as follows:

R:

  build_dir <- "</absolute/path/to/build>/r"  # replace between <>
  dyn.load(paste0(build_dir, "/pileup_events.so"))
  source(paste0(build_dir, "/pileup_events.R"))
  count_events(
    "absolute/path/to/bam",
    "chrX:150"
    # no_overlaps=False,  # optional parameters with default values
    # min_mapq=25,
    # min_baseq=30,
    # include_flag=0,
    # exclude_flag=3844,
    # max_depth=1000000,
    # clip_bound=0
  )

Python:

  # setup in BASH
  pev_bind_path=</path/to/build>/python   # replace between <>
  export PYTHONPATH=${PYTHONPATH}:${pev_bind_path}  # add to python path (not permanent)

  import pileup_events as pev
  help(pev.count_events)
  pev.count_events(
    "absolute/path/to/bam",
    "chrX:100-200"
    # no_overlaps=False,  # optional parameters with default values
    # min_mapq=25,
    # min_baseq=30,
    # include_flag=0,
    # exclude_flag=3844,
    # max_depth=1000000,
    # clip_bound=0
  )

In either case the return value of the count events function is a 1D vector, where each of the genomic positions counted is a block of 24 cells in the vector. It is currently left to the user to transform this strucutre into any desirable alternative.

The compiled bindings directories (python/ and r/) can be renamed, and moved anywhere appropriate on the system. They are not dependent on other build artefacts. Do not modify or rename any of the files within these directories. Note that for the python bindings if you do move/rename the python/ directory you will need to add the new location to PYTHONPATH.

Development & Testing

To enable compliation with debug flags and compilation of the test binary, add the following options to the cmake .. step:

  cmake .. \
    -DENABLE_DEBUG_FLAGS=ON \
    -DMAKE_TEST=ON # \
    # other options

Compliation of the test binary will produce an additional artefact, build/test-pev. Execution of this artefact will run the test suite. The test suite is currently quite brief, and may be expanded upon in the future.

Authors & Acknowledgements

pileup-events is the work of Alex Byrne ([email protected]) & Luca Barbon of CASM Informatics, Wellcome Sanger Institute.

This tool uses htslib for accessing sequence data, and cxxopts for the CLI interface. Testing is made using Catch2

The function of the tool is to provide an standalone version of the bam2R() functionality found in the R package deepSNV. It is a complete rewrite of the concepts found therein.

Citations

htslib:

HTSlib: C library for reading/writing high-throughput sequencing data James K Bonfield, John Marshall, Petr Danecek, Heng Li, Valeriu Ohan, Andrew Whitwham, Thomas Keane, Robert M Davies GigaScience, Volume 10, Issue 2, February 2021, giab007, https://doi.org/10.1093/gigascience/giab007

deepSNV:

Gerstung M, Beisel C, Rechsteiner M, Wild P, Schraml P, Moch H, Beerenwinkel N (2012). “Reliable detection of subclonal single-nucleotide variants in tumor cell populations.” Nat Commun, 3, 811.
Gerstung M, Papaemmanuil E, Campbell PJ (2014). “Subclonal variant calling with multiple samples and prior knowledge.” Bioinformatics, 30, 1198-1204.