Infer and visualize copy number from high-throughput DNA sequencing data.
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  1. {
  2. "fasta": "oss://pgx-reference-data/GRCh38.d1.vd1/GRCh38.d1.vd1.fa",
  3. "faidx": "oss://pgx-reference-data/GRCh38.d1.vd1/GRCh38.d1.vd1.fa.fai",
  4. "docker": "registry.cn-shanghai.aliyuncs.com/pgx-docker-registry/cnvkit:0.9.7",
  5. "disk_size": "400",
  6. "cluster_config": "OnDemand bcs.a2.7xlarge img-ubuntu-vpc",
  7. "bed": "oss://pgx-reference-data/reference/wes_bedfiles/agilent_v6/SureSelect_Human_All_Exon_V6_r2.bed",
  8. "ref_flat": "oss://pgx-reference-data/GRCh38.d1.vd1/refFlat.txt",
  9. "min_gap_size": "5000",
  10. "method": "hybrid",
  11. "segment_method": "cbs"
  12. }