| (** This test uses the high-level EDSL and tries different compilation targets,
but does not produce runnable workflows.
The workflow itself is voluntarily too big and abuses lambda expressions. *) |
open Nonstd
module type TEST_PIPELINE =
functor (Bfx : Biokepi.EDSL.Semantics) ->
sig
val run : unit -> unit Bfx.observation
end
module Run_test(Test_pipeline : TEST_PIPELINE) = struct
let write_file file ~content =
let out_file = open_out file in
try
output_string out_file content;
close_out out_file
with _ ->
close_out out_file
let cmdf fmt =
ksprintf (fun s ->
printf "CMD: %s\n%!" s;
match Sys.command s with
| 0 -> ()
| other -> ksprintf failwith "non-zero-exit: %s -> %d" s other) fmt
let (//) = Filename.concat
let test_dir = "_build/ttfi-test-results/"
let main prefix =
let start_time = Unix.gettimeofday () in
cmdf "mkdir -p %s" test_dir;
let results = ref [] in
let add_result fmt = ksprintf (fun s -> results := s :: !results) fmt in
let add_result_file name path =
let size =
let s = Unix.stat path in
match s.Unix.st_size with
| 0 -> "EMPTY"
| small when small < 1024 -> sprintf "%d B" small
| avg when avg < (1024 * 1024) ->
sprintf "%.2f KB" (float avg /. 1024.)
| big ->
sprintf "%.2f MB" (float big /. (1024. *. 1024.))
in
add_result "%s: `%s` (%s)" name path size;
in
let output_path suffix = test_dir // prefix ^ suffix in
begin
let module Display_pipeline = Test_pipeline(Biokepi.EDSL.Compile.To_display) in
let pseudocode = output_path "-pseudocode.txt" in
write_file pseudocode
~content:(Display_pipeline.run () |> SmartPrint.to_string 80 2);
add_result_file "Pseudo-code" pseudocode;
end;
begin
let module Jsonize_pipeline =
Test_pipeline(Biokepi.EDSL.Compile.To_json) in
let json = output_path ".json" in
write_file json
~content:(Jsonize_pipeline.run ()
|> Yojson.Basic.pretty_to_string ~std:true);
add_result_file "JSON" json;
end;
let output_dot sm dot png =
try
let out = open_out dot in
SmartPrint.to_out_channel 80 2 out sm;
close_out out;
add_result_file "DOT" dot;
let dotlog = png ^ ".log" in
cmdf "dot -v -x -Tpng %s -o %s > %s 2>&1" dot png dotlog;
add_result_file "PNG" png;
with e ->
add_result "FAILED TO OUTPUT: %s (%s)" dot (Printexc.to_string e);
in
begin
let module Dotize_pipeline = Test_pipeline(Biokepi.EDSL.Compile.To_dot) in
let sm_dot = Dotize_pipeline.run () in
let dot = output_path "-1.dot" in
let png = output_path "-1.png" in
output_dot sm_dot dot png
end;
begin
let module Dotize_twice_beta_reduced_pipeline =
Test_pipeline(
Biokepi.EDSL.Transform.Apply_functions(
Biokepi.EDSL.Transform.Apply_functions(
Biokepi.EDSL.Compile.To_dot
)
)
)
in
let dot = output_path "-double-beta.dot" in
let sm_dot = Dotize_twice_beta_reduced_pipeline.run () in
let png = output_path "-double-beta.png" in
output_dot sm_dot dot png
end;
begin
let module Workflow_compiler =
Biokepi.EDSL.Compile.To_workflow.Make(struct
include Biokepi.EDSL.Compile.To_workflow.Defaults
let processors = 42
let work_dir = "/work/dir/"
let machine =
Biokepi.Setup.Build_machine.create
"ssh://example.com/tmp/KT/"
end)
in
let module Ketrew_pipeline = Test_pipeline(Workflow_compiler) in
let workflow =
Ketrew_pipeline.run ()
|> Biokepi.EDSL.Compile.To_workflow.File_type_specification.get_unit_workflow
~name:"Biokepi TTFI test top-level node"
in
ignore workflow
end;
let end_time = Unix.gettimeofday () in
add_result "Total-time: %.2f s" (end_time -. start_time);
List.rev !results
end
module Pipeline_insane (Bfx : Biokepi.EDSL.Semantics) = struct
let fastq_list ~dataset files =
List.map files ~f:begin function
| `Pair (r1, r2) ->
if Filename.check_suffix r1 ".gz"
|| Filename.check_suffix r1 ".fqz"
then
Bfx.(fastq_gz ~sample_name:dataset ~r1 ~r2 () |> gunzip)
else
Bfx.(fastq ~sample_name:dataset ~r1 ~r2 ())
end
|> Bfx.list
let every_vc_on_fastqs ~reference_build ~normal ~tumor =
let aligner which_one =
Bfx.lambda (fun fq -> which_one ~reference_build fq) in
let align_list how (list_of_fastqs : [ `Fastq ] list Bfx.repr) =
Bfx.list_map list_of_fastqs ~f:how |> Bfx.merge_bams
in
let aligners = Bfx.list [
aligner @@ Bfx.bwa_aln ?configuration: None;
aligner @@ Bfx.bwa_mem ?configuration: None;
aligner @@ Bfx.hisat ~configuration:Biokepi.Tools.Hisat.Configuration.default_v1;
aligner @@ Bfx.hisat ~configuration:Biokepi.Tools.Hisat.Configuration.default_v2;
aligner @@ Bfx.star ~configuration:Biokepi.Tools.Star.Configuration.Align.default;
aligner @@ Bfx.mosaik;
aligner @@ (fun ~reference_build fastq ->
Bfx.bwa_aln ~reference_build fastq
|> Bfx.bam_to_fastq ~sample_name:"realigned" `PE
|> Bfx.bwa_mem ?configuration: None ~reference_build
);
] in
let somatic_of_pair how =
Bfx.lambda (fun pair ->
let normal = Bfx.pair_first pair in
let tumor = Bfx.pair_second pair in
how ~normal ~tumor ())
in
let somatic_vcs =
List.map ~f:somatic_of_pair [
Bfx.mutect
~configuration:Biokepi.Tools.Mutect.Configuration.default;
Bfx.mutect2
~configuration:Biokepi.Tools.Gatk.Configuration.Mutect2.default;
Bfx.somaticsniper
~configuration:Biokepi.Tools.Somaticsniper.Configuration.default;
Bfx.strelka
~configuration:Biokepi.Tools.Strelka.Configuration.default;
Bfx.varscan_somatic ?adjust_mapq:None;
Bfx.muse
~configuration:Biokepi.Tools.Muse.Configuration.wes;
Bfx.virmid
~configuration:Biokepi.Tools.Virmid.Configuration.default;
]
in
let aligned_pairs
: (([ `Fastq ] list * [ `Fastq ] list) -> ([ `Bam ] * [ `Bam ]) list) Bfx.repr =
Bfx.lambda (fun pair ->
Bfx.list_map aligners ~f:(
Bfx.lambda (fun (al : ([ `Fastq ] -> [ `Bam ]) Bfx.repr) ->
Bfx.pair
(align_list al (Bfx.pair_first pair : [ `Fastq ] list Bfx.repr))
(align_list al (Bfx.pair_second pair))
)
)
)
in
let vcfs =
Bfx.lambda (fun pair ->
List.map somatic_vcs ~f:(fun vc ->
Bfx.list_map (Bfx.apply aligned_pairs pair) ~f:(
Bfx.lambda (fun bam_pair ->
let (||>) x f = Bfx.apply f x in
let indelreal =
Bfx.lambda (fun pair ->
Bfx.gatk_indel_realigner_joint
~configuration: Biokepi.Tools.Gatk.Configuration.default_indel_realigner
pair)
in
let map_pair f =
Bfx.lambda (fun pair ->
let b1 = Bfx.pair_first pair in
let b2 = Bfx.pair_second pair in
Bfx.pair (f b1) (f b2)
)
in
let bqsr_pair =
Bfx.gatk_bqsr
~configuration: Biokepi.Tools.Gatk.Configuration.default_bqsr
|> map_pair in
let markdups_pair =
Bfx.picard_mark_duplicates
~configuration:Biokepi.Tools.Picard.Mark_duplicates_settings.default
|> map_pair in
bam_pair ||> markdups_pair ||> indelreal ||> bqsr_pair ||> vc
||> Bfx.lambda Bfx.to_unit
)
)
)
|> Bfx.list
)
in
let workflow_of_pair =
Bfx.lambda (fun pair ->
Bfx.list [
(Bfx.apply aligned_pairs pair
|> Bfx.list_map ~f:(Bfx.lambda (fun p ->
Bfx.pair_first p
|> Bfx.stringtie
~configuration:Biokepi.Tools.Stringtie.Configuration.default)
)) |> Bfx.to_unit;
Bfx.apply vcfs pair |> Bfx.to_unit;
begin
Bfx.apply
(Bfx.lambda (fun p -> Bfx.pair_first p |> Bfx.concat |> Bfx.seq2hla))
pair
|> Bfx.to_unit
end;
begin
Bfx.apply
(Bfx.lambda (fun p -> Bfx.pair_second p |> Bfx.concat |> Bfx.optitype `RNA))
pair
|> Bfx.to_unit
end;
begin
Bfx.apply aligned_pairs pair
|> Bfx.list_map ~f:(Bfx.lambda (fun p ->
Bfx.pair_first p
|> Bfx.gatk_haplotype_caller
))
|> Bfx.to_unit
end;
]
|> Bfx.to_unit
)
in
Bfx.apply workflow_of_pair (Bfx.pair normal tumor)
let normal =
("normal-1", [
`Pair ("/input/normal-1-001-r1.fastq", "/input/normal-1-001-r2.fastq");
`Pair ("/input/normal-1-002-r1.fastq", "/input/normal-1-002-r2.fastq");
`Pair ("/input/normal-1-003-r1.fqz", "/input/normal-1-003-r2.fqz");
])
let tumor =
("tumor-1", [
`Pair ("/input/tumor-1-001-r1.fastq.gz", "/input/tumor-1-001-r2.fastq.gz");
`Pair ("/input/tumor-1-002-r1.fastq.gz", "/input/tumor-1-002-r2.fastq.gz");
])
let run () =
Bfx.observe (fun () ->
every_vc_on_fastqs
~reference_build:"b37"
~normal:(fastq_list ~dataset:(fst normal) (snd normal))
~tumor:(fastq_list ~dataset:(fst tumor) (snd tumor))
)
end
module Somatic_simplish(Bfx: Biokepi.EDSL.Semantics) = struct
module Insane_library = Pipeline_insane(Bfx)
let vc =
let normal =
Insane_library.(fastq_list ~dataset:(fst normal) (snd normal))
in
let tumor =
Insane_library.(fastq_list ~dataset:(fst tumor) (snd tumor))
in
let ot_hla =
normal |> Bfx.concat |> Bfx.optitype `DNA |> Bfx.to_unit
in
let align fastq =
Bfx.list_map fastq ~f:(Bfx.lambda (fun fq ->
Bfx.bwa_mem fq
~reference_build:"b37"
|> Bfx.picard_mark_duplicates
~configuration:Biokepi.Tools.Picard.Mark_duplicates_settings.default
)) in
let normal_bam = align normal |> Bfx.merge_bams in
let tumor_bam = align tumor |> Bfx.merge_bams in
let bam_pair = Bfx.pair normal_bam tumor_bam in
let indel_realigned_pair =
Bfx.gatk_indel_realigner_joint bam_pair
~configuration: Biokepi.Tools.Gatk.Configuration.default_indel_realigner
in
let final_normal_bam =
Bfx.pair_first indel_realigned_pair
|> Bfx.gatk_bqsr
~configuration: Biokepi.Tools.Gatk.Configuration.default_bqsr
in
let final_tumor_bam =
Bfx.pair_second indel_realigned_pair
|> Bfx.gatk_bqsr
~configuration: Biokepi.Tools.Gatk.Configuration.default_bqsr
in
let vcfs =
let normal, tumor = final_normal_bam, final_tumor_bam in
Bfx.list [
Bfx.mutect ~normal ~tumor ();
Bfx.somaticsniper ~normal ~tumor ();
Bfx.strelka ~normal ~tumor ();
] in
Bfx.list [
Bfx.to_unit vcfs;
ot_hla;
] |> Bfx.to_unit
let run () =
Bfx.observe (fun () -> vc)
end
let () =
let module Go_insane = Run_test(Pipeline_insane) in
let insane_result = Go_insane.main "pipeline-insane" in
let module Go_simple_somatic = Run_test(Somatic_simplish) in
let simple_somatic_result = Go_simple_somatic.main "pipeline-simple-somatic" in
let display_result mod_name results =
printf "- `%s`:\n%s\n%!"
mod_name
(List.map results ~f:(sprintf " * %s\n") |> String.concat "");
in
printf "\n### Test results:\n\n";
display_result "Pipeline_insane" insane_result;
display_result "Somatic_simplish" simple_somatic_result;
()