EXCAVATE-HT

Contents

  • Introduction
  • Installation
  • Parameters
  • EXCAVATE-HT Modes
  • EXCAVATE-HT Examples
  • API Reference
  • Contributing
EXCAVATE-HT
  • EXCAVATE-HT Documentation
  • View page source

EXCAVATE-HT Documentation

EXCAVATE-HT (EXtraction of Common Allelic VAriants for Targeted Editing in High-Throughput) is a Python-based bioinformatic pipeline to mine population and personalised variant data to identify genomic loci targetable for CRISPR-based allele-specific editing and create single and dual-gRNA libraries to enable high-throughput screens of these edits.

Contents

  • Introduction
  • Installation
    • Prerequisites
    • Set Up
    • Prepare input data files
    • Using EXCAVATE-HT
    • Off-target Analysis Setup
    • Troubleshooting
  • Parameters
  • EXCAVATE-HT Modes
    • excavate-ht generate
    • excavate-ht pair
  • EXCAVATE-HT Examples
    • Example run: Generating a paired dual-gRNA library
    • Example run: Generating a single-gRNA library, editing it, then pairing to create a dual-gRNA library
  • API Reference
    • add_common_args()
    • add_generate_parser()
    • add_pair_parser()
    • apply_pairing()
    • initialize_cas_obj()
    • load_variant_data()
    • main()
    • run_generate()
    • run_off_targets()
    • run_pairing()
    • Cas
    • SaCas9
    • all_guides_var_info()
    • cas_obj
    • count_exact_matches()
    • create_custom_cas_obj()
    • create_exclusion_pos_set()
    • create_gens()
    • create_regex_pam()
    • find_guides()
    • fixed_point_pair()
    • getaltseq()
    • init_worker()
    • makeseq()
    • one_mismatch()
    • output_bed_format()
    • random_pair()
    • search_pattern()
    • split_phased()
    • targetable_vars()
    • tiling_pair()
  • Contributing
    • Reporting Issues

Indices and tables

  • Index

  • Module Index

  • Search Page

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