Integrate the graphs across samples, to form one merged splicing graph (per gene).
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  1. task spladder {
  2. String sample_id
  3. Array[File] bam
  4. Array[File] bai
  5. Array[File] pickle
  6. File reference_gtf_file
  7. String docker
  8. String cluster
  9. String disk_size
  10. command <<<
  11. set -o pipefail
  12. set -e
  13. mkdir -p ${sample_id}/spladder_out/spladder
  14. for i in ${sep=" " bam}
  15. do
  16. echo $i >> alignment.txt
  17. done
  18. for i in ${sep=" " bai}
  19. do
  20. echo $i >> alignment_bai.txt
  21. done
  22. for i in ${sep=" " pickle}
  23. do
  24. ln -s $i ${sample_id}/spladder_out/spladder/
  25. ls ${sample_id}/spladder_out/spladder/ >> pickle.txt
  26. done
  27. spladder build -o ${sample_id}/spladder_out \
  28. --annotation ${reference_gtf_file} \
  29. --bams alignment.txt \
  30. --confidence 2 \
  31. --merge-strat merge_graphs \
  32. --validate-sg \
  33. --readlen 150 \
  34. --parallel 4 \
  35. --event-types exon_skip,intron_retention,alt_3prime,alt_5prime,mutex_exons,mult_exon_skip
  36. find . -depth > fileList.txt
  37. >>>
  38. runtime {
  39. docker: docker
  40. cluster: cluster
  41. systemDisk: "cloud_ssd 40"
  42. dataDisk: "cloud_ssd " + disk_size + " /cromwell_root/"
  43. }
  44. output {
  45. File fileList = "fileList.txt"
  46. File alignment = "alignment.txt"
  47. File alignment_bai = "alignment_bai.txt"
  48. File pickle_txt = "pickle.txt"
  49. Array[File] AS_gff = glob("${sample_id}/spladder_out/*.gff3")
  50. Array[File] AS_pickle = glob("${sample_id}/spladder_out/*.pickle")
  51. Array[File] AS_gz = glob("${sample_id}/spladder_out/*.gz")
  52. Array[File] AS_hdf5 = glob("${sample_id}/spladder_out/*.hdf5")
  53. Array[File] spladder = glob("${sample_id}/spladder_out/spladder/*")
  54. Array[File] tmp = glob("${sample_id}/spladder_out/tmp/*")
  55. }
  56. }