wildlamp 1.0.1__tar.gz

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wildlamp-1.0.1/LICENSE ADDED
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+ Metadata-Version: 2.4
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+ Name: wildlamp
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+ Version: 1.0.1
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+ Summary: A computational pipeline for designing conserved RT-LAMP primers across genomically uncharacterised wildlife species.
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+ Author-email: Thomas Stocker <thomas.stocker@sydney.edu.au>
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+ Requires-Python: >=3.9
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+ Description-Content-Type: text/markdown
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+ License-File: LICENSE
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+ Requires-Dist: biopython>=1.80
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+ Requires-Dist: numpy>=1.23
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+ Requires-Dist: pandas>=1.5
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+ Requires-Dist: matplotlib>=3.6
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+ Requires-Dist: requests>=2.28
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+ Requires-Dist: primer3-py>=0.7
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+ Requires-Dist: viennarna>=2.6
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+ Provides-Extra: dev
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+ Requires-Dist: pytest; extra == "dev"
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+ Requires-Dist: black; extra == "dev"
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+ Requires-Dist: ruff; extra == "dev"
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+ Requires-Dist: mypy; extra == "dev"
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+ Dynamic: license-file
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+
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+ # wildlamp: a tool for identification of primer binding sites among conserved gene families of primers.
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+
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+ This package enables the construction of the LAMP primers, their optimisation and checking for quality/ cross-reactivity. The package can be downloaded as:
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+
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+ ```
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+ pip install wildlamp
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+ ```
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+
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+ The main command for the construction of LAMP primers is the command:
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+
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+ ```
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+ init_primers(alignment_path, output="fill in for your specified output.csv")
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+ ```
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+
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+ Where the user specifies the file path for the aligned set of sequences and the rest occurs by computer.
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+
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+ Following on from that the user can retrieve the species from the aligned sequence accessions provided they are from NCBI, using the command:
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+
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+ ```
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+ species_fetch(csv_file)
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+ ```
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+
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+ The primers can then be checked for hits against the genome of a species of their choice using either the csv2hits or the primer2hits command.
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+
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+ ```
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+ csv2hits(csv_file, taxid, output="fill in your preferred output prefix.csv")
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+
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+ # or use this command if you want to specify your own primers independent of the csv
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+ panel: [
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+ {"FIP": "ATCG...", "BIP": "GGTA..."},
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+ {"FIP": "...", "BIP": "..."},
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+ ...
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+ ]
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+
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+ primers2hits(panel, taxid, output="preferred specified csv output")
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+ ```
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+
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+ The final primers can be generated through the command:
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+
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+ ```
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+ final_primers(alignment_path, primer_csv_path, output="preferred csv output")
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+ ```
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+
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+ The final perturbation checks can be performed with the command below - with both lightweight and heavy perturbation analysis. Heavyweight analysis is primer-thermodynamic stress test and the lightweight is a biological/ transcript specificity/ sensitivity analysis... or more simply a multitransript mismatch scan. The first transcript in the fasta file is assumed to be the reference for the heavyweight analysis. Note only use unaligned fasta files for this section. The command can be called by:
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+
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+ ```
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+ final_perturbation(unaligned_fasta_path,
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+ primer_csv_path_from_earlier,
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+ output="perturbation_output.csv path")
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+ ```
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+
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+ Final validation check for the primer sets:
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+
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+ ```
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+ final_valid(primer_csv_path, unaligned_fasta_path, output="output csv file")
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+ ```
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+
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+ Once the primers are settled, run the csv file through this code to generate the standard curve. But the csv must be edited first to have a column "Gene" and "fasta":
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+ ```
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+ stand_curves(primer_gene_csv_path, output="standard_curve.csv, but fill in yourself")
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+ ```
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+
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+ If one wants to run the standard curve quantification in the absence of experimental data the following code will do that, but first caveates, must fill in the user R, G, B values, the gene name in the csv, the curve_csv from the step above, the output and the dilution factor. The dilution factor is 1:X where X is the user specified value:
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+ ```
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+ estimate_copies(user_R, user_G, user_B,
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+ gene_name, curve_csv,
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+ output="final_csv.csv",
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+ dilution_factor=1)
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+ ```
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+
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+ File directory is below:
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+
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+ ```
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+ wildlamp/
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+ |
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+ |-- alignment/
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+ | |-- conservation.py # compute_conservation
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+ | |-- load_seq.py # load_alignment and clean_alignment
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+ |
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+ |-- data/
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+ | |-- csv_results/
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+ | | |-- FILL IN LATER
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+ | |
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+ | |-- study_fasta/
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+ | | |-- DIO1_N_fur.fasta # DIO1 reference for followup
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+ | | |-- DIO1_pinniped_aligned.fasta # DIO1 aligned
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+ | | |-- DIO1_pinniped.fasta # unaligned
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+ | | |-- DIO2_N_fur.fasta # DIO2 reference
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+ | | |-- DIO2_pinniped_aligned.fasta # DIO2 aligned
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+ | | |-- DIO2_pinniped.fasta # DIO2 unaligned
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+ | | |-- DIO3_N_fur.fasta # DIO3 reference
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+ | | |-- DIO3_pinnipedia.fas # DIO3 ALIGNED
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+ | | |-- DIO3_pinnipeds.fasta # DIO3 UNALIGNED
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+ | | |-- HSP70_all_aligned.fasta # HSP70 aligned
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+ | | |-- HSP70_all.fasta # HSP70 unaligned
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+ | | |-- HSP70_N_fur.fasta # HSP70 reference
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+ | | |-- plasminogen_receptor_aligned.fasta # plasminogen receptor aligned
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+ | | |-- plasminogen_receptor.fasta # plasminogen receptor unaligned (note no ref - not studied)
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+ | | |-- slc25a43_aligned.fasta # slc25a43 aligned
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+ | | |-- slc25a43_N_fur.fasta # slc25a43 reference
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+ | | |-- slc25a43.fasta # unaligned
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+ |
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+ |-- failures/
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+ | |-- debug.py # debug_no_matches
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+ | |-- failure_mode.py # analyze_failure_modes
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+ | |-- suggest.py # suggest_degenerate
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+ |
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+ |-- perturbation/
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+ | |-- analysis.py # perturbation_analysis
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+ | |-- best_mismatch_score.py # best_mismatch_score, find_best_matches
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+ | |-- mismatch_counter.py # best_match
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+ | |-- mutate.py # mutate_base and perturb_primer
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+ | |-- robustness.py # built_robustness_matrix, compute_perturbation_robustness_scores
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+ |
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+ |-- pipeline/
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+ | |-- conc.py # estimate_copies
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+ | |-- csv2hits.py # csv2hits
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+ | |-- final_perturb.py # fianl_perturbation
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+ | |-- final_primers.py # final_primers
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+ | |-- init_primers.py # init_primers
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+ | |-- primer2hits.py # primers2hits
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+ | |-- species_fetch.py # species_fetch
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+ | |-- stand_curve.py # stand_curve
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+ | |-- validate.py # final_validate
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+ |
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+ |-- primer_hits/
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+ | |-- crossreactive.py # blast_sequence, biologically_meaningful
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+ |
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+ |-- primers/
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+ | |-- amplicons.py # amplicon_heuristic and amplicon_score
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+ | |-- analyse_primer_rows.py # analyse_row
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+ | |-- build_full_lset.py # build_full_lset
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+ | |-- clash.py # primer_clash, build_clash_map
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+ | |-- detect_lamp.py # detect_lamp_sets
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+ | |-- lamp_score.py # primer_basic_score, primer_thermo_score, primer_struct_score
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+ | | # primer_conservation_score, lamp_score, rtlamp_score
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+ | |-- mismatch.py # mismatch_cost
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+ | |-- optimise_primer.py # optimise_primer
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+ | |-- primer_from_csv.py # load_primers_from_csv
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+ | |-- scan.py # primer_ok, scan_primers
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+ | |-- species.py # primer_species_coverage, filter_primers_by_species
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+ |
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+ |-- scripts/ # contains the scripts used in the study
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+ | |-- acc2spp.py # extract_accession, accession_to_gene_id, get_species_from_accession,
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+ | | # extract_accessions_from_csv, write_species_lookup
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+ | |-- fasta-stats.py # no commands - just basic code
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+ | |-- final_dilution-LoD_3.py # rc, build_FIP, build_BIP, load_gene, best_match_mismatches,
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+ | | # compute_hairpin, compute_homodimer, compute_heterodimer,
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+ | | # has_3prime_dimer, compute_primer_features,
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+ | | # fraction_sequestered, fraction_free, binding_efficiency,
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+ | | # dimer_sink_factor, lamp_tm_score,
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+ | | # lamp_primer_biophysical_score, rt_lamp_rate, simulate_rt_qlamp
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+ | | # color_hnb_from_copies, color_pr_from_copies, delta_rgb,
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+ | | # simulate_quant_curve, fit_standard_curve,
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+ | | # copies_from_Tt_colour, plot_multi_gene_curve, plot_delta_rgb,
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+ | | # generate_all_thermo_tables, write_thermo_csv,
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+ | | # generate_standard_curve_summary, main
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+ | |-- final-validation.py # load_gene, gc_content, fold_rna, best_match, binding_accessibility
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+ | | # thermo, analyse_gene, write_gene_tables, write_gc_table,
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+ | | # write_long_all, main
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+ | |-- LAMP_Assay.py # load_alignment, clean_alignment, compute_conservation, gc, bad_run,
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+ | | # mismatch_cost, primers_ok, scan_primers, primer_species_coverage,
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+ | | # filter_primers_by_species, species_coverage, primers_clash,
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+ | | # build_clash_map, amplicon_heuristic, detect_lamp_sets, evaluate_primer3,
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+ | | # vienna_fold_dna, validate_primer_vienna, validate_lamp_set_vienna,
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+ | | # primer_basic_score, primer_thermo_score, primer_struct_score,
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+ | | # primer_conservation_score, amplicon_score, lamp_score, rtlamp_score,
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+ | | # suggest_degenerate, analyze_failure_modes, mutate_base, perturb_primer,
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+ | | # perturbation_analysis, build_robustness_matrix,
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+ | | # compute_perturbation_robustness_scores, debug_no_matches, main
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+ | |-- LAMP-hits.py # blast_sequences, biologically_meaningful
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+ | |-- pertubation_final.py # best_mismatch_score,
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+ | |-- primer_optimise.py # load_alignment, clean_alignment, gc, bad_run, rc, mismatch_cost,
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+ | # primer_species_coverage, thermo_score, primer_ok, optimise_primer,
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+ | # vienna_fold_dna, vienna_validate_set, mutate_base, perturb_primer,
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+ | # perturbation_analysis, compute_robustness_score, build_full_lset, main
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+ |
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+ |-- simulations/
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+ | |-- curve_fit.py # fit_standard_curve, copies_from_Tt
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+ | |-- dye.py # color_pr_from_copies, delta_rgb, parameters: PR_BASELINE
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+ | |-- model_rtlamp.py # best_match_mismatches, compute_hairpin, compute_homodimer,
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+ | | # compute_heterodimer, has_3prime_dimer, compute_primer_features,
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+ | | # fraction_sequestered, fraction_free, binding_efficiency,
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+ | | # dimer_sink_factor, lamp_tm_score, lamp_primer_biophysical_score,
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+ | | # rt_lamp_rate, simulate_rt_qlamp
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+ | |-- sim_curve.py # simulate_quant_curve_pr, parameters: QUANT_CONC
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+ |
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+ |-- species/
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+ | |-- accession.py # extract_accession, extract_accessions_from_csv
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+ | |-- ncbi_lookup.py # accession_to_gene_id, get_species_from_accession
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+ | |-- table.py # write_species_lookup
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+ |
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+ |-- thermodynamics/
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+ | |-- fold_rna.py # fold_rna
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+ | |-- primer_access.py # binding_accessibility
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+ | |-- primer3_eval.py # evaluate_primer3
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+ | |-- scoring.py # thermo_score
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+ | |-- simple_thermo.py # thermo
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+ | |-- vienna_eval.py # vienna_fold_dna, validate_primer_vienna, validate_lamp_set_vienna
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+ |
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+ |-- utils/
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+ | |-- build_primers.py # build_BIP, build_FIP
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+ | |-- gc_content.py # gc_content
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+ | |-- gene_primer.py # load_gene_primer_csv
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+ | |-- load_seq.py # load_primers_csv, load_fasta
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+ | |-- seq.py # gc, bad_run, rc
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+ | |-- valid_csv_write.py # write_outputs
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+ |
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+ |-- __init__.py
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+ |-- LICENSE # open access code - must cite
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+ |-- README.md
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+ ```
@@ -0,0 +1,212 @@
1
+ # wildlamp: a tool for identification of primer binding sites among conserved gene families of primers.
2
+
3
+ This package enables the construction of the LAMP primers, their optimisation and checking for quality/ cross-reactivity. The package can be downloaded as:
4
+
5
+ ```
6
+ pip install wildlamp
7
+ ```
8
+
9
+ The main command for the construction of LAMP primers is the command:
10
+
11
+ ```
12
+ init_primers(alignment_path, output="fill in for your specified output.csv")
13
+ ```
14
+
15
+ Where the user specifies the file path for the aligned set of sequences and the rest occurs by computer.
16
+
17
+ Following on from that the user can retrieve the species from the aligned sequence accessions provided they are from NCBI, using the command:
18
+
19
+ ```
20
+ species_fetch(csv_file)
21
+ ```
22
+
23
+ The primers can then be checked for hits against the genome of a species of their choice using either the csv2hits or the primer2hits command.
24
+
25
+ ```
26
+ csv2hits(csv_file, taxid, output="fill in your preferred output prefix.csv")
27
+
28
+ # or use this command if you want to specify your own primers independent of the csv
29
+ panel: [
30
+ {"FIP": "ATCG...", "BIP": "GGTA..."},
31
+ {"FIP": "...", "BIP": "..."},
32
+ ...
33
+ ]
34
+
35
+ primers2hits(panel, taxid, output="preferred specified csv output")
36
+ ```
37
+
38
+ The final primers can be generated through the command:
39
+
40
+ ```
41
+ final_primers(alignment_path, primer_csv_path, output="preferred csv output")
42
+ ```
43
+
44
+ The final perturbation checks can be performed with the command below - with both lightweight and heavy perturbation analysis. Heavyweight analysis is primer-thermodynamic stress test and the lightweight is a biological/ transcript specificity/ sensitivity analysis... or more simply a multitransript mismatch scan. The first transcript in the fasta file is assumed to be the reference for the heavyweight analysis. Note only use unaligned fasta files for this section. The command can be called by:
45
+
46
+ ```
47
+ final_perturbation(unaligned_fasta_path,
48
+ primer_csv_path_from_earlier,
49
+ output="perturbation_output.csv path")
50
+ ```
51
+
52
+ Final validation check for the primer sets:
53
+
54
+ ```
55
+ final_valid(primer_csv_path, unaligned_fasta_path, output="output csv file")
56
+ ```
57
+
58
+ Once the primers are settled, run the csv file through this code to generate the standard curve. But the csv must be edited first to have a column "Gene" and "fasta":
59
+ ```
60
+ stand_curves(primer_gene_csv_path, output="standard_curve.csv, but fill in yourself")
61
+ ```
62
+
63
+ If one wants to run the standard curve quantification in the absence of experimental data the following code will do that, but first caveates, must fill in the user R, G, B values, the gene name in the csv, the curve_csv from the step above, the output and the dilution factor. The dilution factor is 1:X where X is the user specified value:
64
+ ```
65
+ estimate_copies(user_R, user_G, user_B,
66
+ gene_name, curve_csv,
67
+ output="final_csv.csv",
68
+ dilution_factor=1)
69
+ ```
70
+
71
+ File directory is below:
72
+
73
+ ```
74
+ wildlamp/
75
+ |
76
+ |-- alignment/
77
+ | |-- conservation.py # compute_conservation
78
+ | |-- load_seq.py # load_alignment and clean_alignment
79
+ |
80
+ |-- data/
81
+ | |-- csv_results/
82
+ | | |-- FILL IN LATER
83
+ | |
84
+ | |-- study_fasta/
85
+ | | |-- DIO1_N_fur.fasta # DIO1 reference for followup
86
+ | | |-- DIO1_pinniped_aligned.fasta # DIO1 aligned
87
+ | | |-- DIO1_pinniped.fasta # unaligned
88
+ | | |-- DIO2_N_fur.fasta # DIO2 reference
89
+ | | |-- DIO2_pinniped_aligned.fasta # DIO2 aligned
90
+ | | |-- DIO2_pinniped.fasta # DIO2 unaligned
91
+ | | |-- DIO3_N_fur.fasta # DIO3 reference
92
+ | | |-- DIO3_pinnipedia.fas # DIO3 ALIGNED
93
+ | | |-- DIO3_pinnipeds.fasta # DIO3 UNALIGNED
94
+ | | |-- HSP70_all_aligned.fasta # HSP70 aligned
95
+ | | |-- HSP70_all.fasta # HSP70 unaligned
96
+ | | |-- HSP70_N_fur.fasta # HSP70 reference
97
+ | | |-- plasminogen_receptor_aligned.fasta # plasminogen receptor aligned
98
+ | | |-- plasminogen_receptor.fasta # plasminogen receptor unaligned (note no ref - not studied)
99
+ | | |-- slc25a43_aligned.fasta # slc25a43 aligned
100
+ | | |-- slc25a43_N_fur.fasta # slc25a43 reference
101
+ | | |-- slc25a43.fasta # unaligned
102
+ |
103
+ |-- failures/
104
+ | |-- debug.py # debug_no_matches
105
+ | |-- failure_mode.py # analyze_failure_modes
106
+ | |-- suggest.py # suggest_degenerate
107
+ |
108
+ |-- perturbation/
109
+ | |-- analysis.py # perturbation_analysis
110
+ | |-- best_mismatch_score.py # best_mismatch_score, find_best_matches
111
+ | |-- mismatch_counter.py # best_match
112
+ | |-- mutate.py # mutate_base and perturb_primer
113
+ | |-- robustness.py # built_robustness_matrix, compute_perturbation_robustness_scores
114
+ |
115
+ |-- pipeline/
116
+ | |-- conc.py # estimate_copies
117
+ | |-- csv2hits.py # csv2hits
118
+ | |-- final_perturb.py # fianl_perturbation
119
+ | |-- final_primers.py # final_primers
120
+ | |-- init_primers.py # init_primers
121
+ | |-- primer2hits.py # primers2hits
122
+ | |-- species_fetch.py # species_fetch
123
+ | |-- stand_curve.py # stand_curve
124
+ | |-- validate.py # final_validate
125
+ |
126
+ |-- primer_hits/
127
+ | |-- crossreactive.py # blast_sequence, biologically_meaningful
128
+ |
129
+ |-- primers/
130
+ | |-- amplicons.py # amplicon_heuristic and amplicon_score
131
+ | |-- analyse_primer_rows.py # analyse_row
132
+ | |-- build_full_lset.py # build_full_lset
133
+ | |-- clash.py # primer_clash, build_clash_map
134
+ | |-- detect_lamp.py # detect_lamp_sets
135
+ | |-- lamp_score.py # primer_basic_score, primer_thermo_score, primer_struct_score
136
+ | | # primer_conservation_score, lamp_score, rtlamp_score
137
+ | |-- mismatch.py # mismatch_cost
138
+ | |-- optimise_primer.py # optimise_primer
139
+ | |-- primer_from_csv.py # load_primers_from_csv
140
+ | |-- scan.py # primer_ok, scan_primers
141
+ | |-- species.py # primer_species_coverage, filter_primers_by_species
142
+ |
143
+ |-- scripts/ # contains the scripts used in the study
144
+ | |-- acc2spp.py # extract_accession, accession_to_gene_id, get_species_from_accession,
145
+ | | # extract_accessions_from_csv, write_species_lookup
146
+ | |-- fasta-stats.py # no commands - just basic code
147
+ | |-- final_dilution-LoD_3.py # rc, build_FIP, build_BIP, load_gene, best_match_mismatches,
148
+ | | # compute_hairpin, compute_homodimer, compute_heterodimer,
149
+ | | # has_3prime_dimer, compute_primer_features,
150
+ | | # fraction_sequestered, fraction_free, binding_efficiency,
151
+ | | # dimer_sink_factor, lamp_tm_score,
152
+ | | # lamp_primer_biophysical_score, rt_lamp_rate, simulate_rt_qlamp
153
+ | | # color_hnb_from_copies, color_pr_from_copies, delta_rgb,
154
+ | | # simulate_quant_curve, fit_standard_curve,
155
+ | | # copies_from_Tt_colour, plot_multi_gene_curve, plot_delta_rgb,
156
+ | | # generate_all_thermo_tables, write_thermo_csv,
157
+ | | # generate_standard_curve_summary, main
158
+ | |-- final-validation.py # load_gene, gc_content, fold_rna, best_match, binding_accessibility
159
+ | | # thermo, analyse_gene, write_gene_tables, write_gc_table,
160
+ | | # write_long_all, main
161
+ | |-- LAMP_Assay.py # load_alignment, clean_alignment, compute_conservation, gc, bad_run,
162
+ | | # mismatch_cost, primers_ok, scan_primers, primer_species_coverage,
163
+ | | # filter_primers_by_species, species_coverage, primers_clash,
164
+ | | # build_clash_map, amplicon_heuristic, detect_lamp_sets, evaluate_primer3,
165
+ | | # vienna_fold_dna, validate_primer_vienna, validate_lamp_set_vienna,
166
+ | | # primer_basic_score, primer_thermo_score, primer_struct_score,
167
+ | | # primer_conservation_score, amplicon_score, lamp_score, rtlamp_score,
168
+ | | # suggest_degenerate, analyze_failure_modes, mutate_base, perturb_primer,
169
+ | | # perturbation_analysis, build_robustness_matrix,
170
+ | | # compute_perturbation_robustness_scores, debug_no_matches, main
171
+ | |-- LAMP-hits.py # blast_sequences, biologically_meaningful
172
+ | |-- pertubation_final.py # best_mismatch_score,
173
+ | |-- primer_optimise.py # load_alignment, clean_alignment, gc, bad_run, rc, mismatch_cost,
174
+ | # primer_species_coverage, thermo_score, primer_ok, optimise_primer,
175
+ | # vienna_fold_dna, vienna_validate_set, mutate_base, perturb_primer,
176
+ | # perturbation_analysis, compute_robustness_score, build_full_lset, main
177
+ |
178
+ |-- simulations/
179
+ | |-- curve_fit.py # fit_standard_curve, copies_from_Tt
180
+ | |-- dye.py # color_pr_from_copies, delta_rgb, parameters: PR_BASELINE
181
+ | |-- model_rtlamp.py # best_match_mismatches, compute_hairpin, compute_homodimer,
182
+ | | # compute_heterodimer, has_3prime_dimer, compute_primer_features,
183
+ | | # fraction_sequestered, fraction_free, binding_efficiency,
184
+ | | # dimer_sink_factor, lamp_tm_score, lamp_primer_biophysical_score,
185
+ | | # rt_lamp_rate, simulate_rt_qlamp
186
+ | |-- sim_curve.py # simulate_quant_curve_pr, parameters: QUANT_CONC
187
+ |
188
+ |-- species/
189
+ | |-- accession.py # extract_accession, extract_accessions_from_csv
190
+ | |-- ncbi_lookup.py # accession_to_gene_id, get_species_from_accession
191
+ | |-- table.py # write_species_lookup
192
+ |
193
+ |-- thermodynamics/
194
+ | |-- fold_rna.py # fold_rna
195
+ | |-- primer_access.py # binding_accessibility
196
+ | |-- primer3_eval.py # evaluate_primer3
197
+ | |-- scoring.py # thermo_score
198
+ | |-- simple_thermo.py # thermo
199
+ | |-- vienna_eval.py # vienna_fold_dna, validate_primer_vienna, validate_lamp_set_vienna
200
+ |
201
+ |-- utils/
202
+ | |-- build_primers.py # build_BIP, build_FIP
203
+ | |-- gc_content.py # gc_content
204
+ | |-- gene_primer.py # load_gene_primer_csv
205
+ | |-- load_seq.py # load_primers_csv, load_fasta
206
+ | |-- seq.py # gc, bad_run, rc
207
+ | |-- valid_csv_write.py # write_outputs
208
+ |
209
+ |-- __init__.py
210
+ |-- LICENSE # open access code - must cite
211
+ |-- README.md
212
+ ```
@@ -0,0 +1,34 @@
1
+ [project]
2
+ name = "wildlamp"
3
+ version = "1.0.1"
4
+ description = "A computational pipeline for designing conserved RT-LAMP primers across genomically uncharacterised wildlife species."
5
+ authors = [
6
+ { name = "Thomas Stocker", email = "thomas.stocker@sydney.edu.au" }
7
+ ]
8
+ readme = "README.md"
9
+ requires-python = ">=3.9"
10
+
11
+ dependencies = [
12
+ "biopython>=1.80",
13
+ "numpy>=1.23",
14
+ "pandas>=1.5",
15
+ "matplotlib>=3.6",
16
+ "requests>=2.28",
17
+ "primer3-py>=0.7",
18
+ "viennarna>=2.6",
19
+ ]
20
+
21
+ [project.optional-dependencies]
22
+ dev = [
23
+ "pytest",
24
+ "black",
25
+ "ruff",
26
+ "mypy"
27
+ ]
28
+
29
+ [build-system]
30
+ requires = ["setuptools>=65", "wheel"]
31
+ build-backend = "setuptools.build_meta"
32
+
33
+ [tool.setuptools.packages.find]
34
+ include = ["wildlamp*"]
@@ -0,0 +1,4 @@
1
+ [egg_info]
2
+ tag_build =
3
+ tag_date = 0
4
+
@@ -0,0 +1,234 @@
1
+ Metadata-Version: 2.4
2
+ Name: wildlamp
3
+ Version: 1.0.1
4
+ Summary: A computational pipeline for designing conserved RT-LAMP primers across genomically uncharacterised wildlife species.
5
+ Author-email: Thomas Stocker <thomas.stocker@sydney.edu.au>
6
+ Requires-Python: >=3.9
7
+ Description-Content-Type: text/markdown
8
+ License-File: LICENSE
9
+ Requires-Dist: biopython>=1.80
10
+ Requires-Dist: numpy>=1.23
11
+ Requires-Dist: pandas>=1.5
12
+ Requires-Dist: matplotlib>=3.6
13
+ Requires-Dist: requests>=2.28
14
+ Requires-Dist: primer3-py>=0.7
15
+ Requires-Dist: viennarna>=2.6
16
+ Provides-Extra: dev
17
+ Requires-Dist: pytest; extra == "dev"
18
+ Requires-Dist: black; extra == "dev"
19
+ Requires-Dist: ruff; extra == "dev"
20
+ Requires-Dist: mypy; extra == "dev"
21
+ Dynamic: license-file
22
+
23
+ # wildlamp: a tool for identification of primer binding sites among conserved gene families of primers.
24
+
25
+ This package enables the construction of the LAMP primers, their optimisation and checking for quality/ cross-reactivity. The package can be downloaded as:
26
+
27
+ ```
28
+ pip install wildlamp
29
+ ```
30
+
31
+ The main command for the construction of LAMP primers is the command:
32
+
33
+ ```
34
+ init_primers(alignment_path, output="fill in for your specified output.csv")
35
+ ```
36
+
37
+ Where the user specifies the file path for the aligned set of sequences and the rest occurs by computer.
38
+
39
+ Following on from that the user can retrieve the species from the aligned sequence accessions provided they are from NCBI, using the command:
40
+
41
+ ```
42
+ species_fetch(csv_file)
43
+ ```
44
+
45
+ The primers can then be checked for hits against the genome of a species of their choice using either the csv2hits or the primer2hits command.
46
+
47
+ ```
48
+ csv2hits(csv_file, taxid, output="fill in your preferred output prefix.csv")
49
+
50
+ # or use this command if you want to specify your own primers independent of the csv
51
+ panel: [
52
+ {"FIP": "ATCG...", "BIP": "GGTA..."},
53
+ {"FIP": "...", "BIP": "..."},
54
+ ...
55
+ ]
56
+
57
+ primers2hits(panel, taxid, output="preferred specified csv output")
58
+ ```
59
+
60
+ The final primers can be generated through the command:
61
+
62
+ ```
63
+ final_primers(alignment_path, primer_csv_path, output="preferred csv output")
64
+ ```
65
+
66
+ The final perturbation checks can be performed with the command below - with both lightweight and heavy perturbation analysis. Heavyweight analysis is primer-thermodynamic stress test and the lightweight is a biological/ transcript specificity/ sensitivity analysis... or more simply a multitransript mismatch scan. The first transcript in the fasta file is assumed to be the reference for the heavyweight analysis. Note only use unaligned fasta files for this section. The command can be called by:
67
+
68
+ ```
69
+ final_perturbation(unaligned_fasta_path,
70
+ primer_csv_path_from_earlier,
71
+ output="perturbation_output.csv path")
72
+ ```
73
+
74
+ Final validation check for the primer sets:
75
+
76
+ ```
77
+ final_valid(primer_csv_path, unaligned_fasta_path, output="output csv file")
78
+ ```
79
+
80
+ Once the primers are settled, run the csv file through this code to generate the standard curve. But the csv must be edited first to have a column "Gene" and "fasta":
81
+ ```
82
+ stand_curves(primer_gene_csv_path, output="standard_curve.csv, but fill in yourself")
83
+ ```
84
+
85
+ If one wants to run the standard curve quantification in the absence of experimental data the following code will do that, but first caveates, must fill in the user R, G, B values, the gene name in the csv, the curve_csv from the step above, the output and the dilution factor. The dilution factor is 1:X where X is the user specified value:
86
+ ```
87
+ estimate_copies(user_R, user_G, user_B,
88
+ gene_name, curve_csv,
89
+ output="final_csv.csv",
90
+ dilution_factor=1)
91
+ ```
92
+
93
+ File directory is below:
94
+
95
+ ```
96
+ wildlamp/
97
+ |
98
+ |-- alignment/
99
+ | |-- conservation.py # compute_conservation
100
+ | |-- load_seq.py # load_alignment and clean_alignment
101
+ |
102
+ |-- data/
103
+ | |-- csv_results/
104
+ | | |-- FILL IN LATER
105
+ | |
106
+ | |-- study_fasta/
107
+ | | |-- DIO1_N_fur.fasta # DIO1 reference for followup
108
+ | | |-- DIO1_pinniped_aligned.fasta # DIO1 aligned
109
+ | | |-- DIO1_pinniped.fasta # unaligned
110
+ | | |-- DIO2_N_fur.fasta # DIO2 reference
111
+ | | |-- DIO2_pinniped_aligned.fasta # DIO2 aligned
112
+ | | |-- DIO2_pinniped.fasta # DIO2 unaligned
113
+ | | |-- DIO3_N_fur.fasta # DIO3 reference
114
+ | | |-- DIO3_pinnipedia.fas # DIO3 ALIGNED
115
+ | | |-- DIO3_pinnipeds.fasta # DIO3 UNALIGNED
116
+ | | |-- HSP70_all_aligned.fasta # HSP70 aligned
117
+ | | |-- HSP70_all.fasta # HSP70 unaligned
118
+ | | |-- HSP70_N_fur.fasta # HSP70 reference
119
+ | | |-- plasminogen_receptor_aligned.fasta # plasminogen receptor aligned
120
+ | | |-- plasminogen_receptor.fasta # plasminogen receptor unaligned (note no ref - not studied)
121
+ | | |-- slc25a43_aligned.fasta # slc25a43 aligned
122
+ | | |-- slc25a43_N_fur.fasta # slc25a43 reference
123
+ | | |-- slc25a43.fasta # unaligned
124
+ |
125
+ |-- failures/
126
+ | |-- debug.py # debug_no_matches
127
+ | |-- failure_mode.py # analyze_failure_modes
128
+ | |-- suggest.py # suggest_degenerate
129
+ |
130
+ |-- perturbation/
131
+ | |-- analysis.py # perturbation_analysis
132
+ | |-- best_mismatch_score.py # best_mismatch_score, find_best_matches
133
+ | |-- mismatch_counter.py # best_match
134
+ | |-- mutate.py # mutate_base and perturb_primer
135
+ | |-- robustness.py # built_robustness_matrix, compute_perturbation_robustness_scores
136
+ |
137
+ |-- pipeline/
138
+ | |-- conc.py # estimate_copies
139
+ | |-- csv2hits.py # csv2hits
140
+ | |-- final_perturb.py # fianl_perturbation
141
+ | |-- final_primers.py # final_primers
142
+ | |-- init_primers.py # init_primers
143
+ | |-- primer2hits.py # primers2hits
144
+ | |-- species_fetch.py # species_fetch
145
+ | |-- stand_curve.py # stand_curve
146
+ | |-- validate.py # final_validate
147
+ |
148
+ |-- primer_hits/
149
+ | |-- crossreactive.py # blast_sequence, biologically_meaningful
150
+ |
151
+ |-- primers/
152
+ | |-- amplicons.py # amplicon_heuristic and amplicon_score
153
+ | |-- analyse_primer_rows.py # analyse_row
154
+ | |-- build_full_lset.py # build_full_lset
155
+ | |-- clash.py # primer_clash, build_clash_map
156
+ | |-- detect_lamp.py # detect_lamp_sets
157
+ | |-- lamp_score.py # primer_basic_score, primer_thermo_score, primer_struct_score
158
+ | | # primer_conservation_score, lamp_score, rtlamp_score
159
+ | |-- mismatch.py # mismatch_cost
160
+ | |-- optimise_primer.py # optimise_primer
161
+ | |-- primer_from_csv.py # load_primers_from_csv
162
+ | |-- scan.py # primer_ok, scan_primers
163
+ | |-- species.py # primer_species_coverage, filter_primers_by_species
164
+ |
165
+ |-- scripts/ # contains the scripts used in the study
166
+ | |-- acc2spp.py # extract_accession, accession_to_gene_id, get_species_from_accession,
167
+ | | # extract_accessions_from_csv, write_species_lookup
168
+ | |-- fasta-stats.py # no commands - just basic code
169
+ | |-- final_dilution-LoD_3.py # rc, build_FIP, build_BIP, load_gene, best_match_mismatches,
170
+ | | # compute_hairpin, compute_homodimer, compute_heterodimer,
171
+ | | # has_3prime_dimer, compute_primer_features,
172
+ | | # fraction_sequestered, fraction_free, binding_efficiency,
173
+ | | # dimer_sink_factor, lamp_tm_score,
174
+ | | # lamp_primer_biophysical_score, rt_lamp_rate, simulate_rt_qlamp
175
+ | | # color_hnb_from_copies, color_pr_from_copies, delta_rgb,
176
+ | | # simulate_quant_curve, fit_standard_curve,
177
+ | | # copies_from_Tt_colour, plot_multi_gene_curve, plot_delta_rgb,
178
+ | | # generate_all_thermo_tables, write_thermo_csv,
179
+ | | # generate_standard_curve_summary, main
180
+ | |-- final-validation.py # load_gene, gc_content, fold_rna, best_match, binding_accessibility
181
+ | | # thermo, analyse_gene, write_gene_tables, write_gc_table,
182
+ | | # write_long_all, main
183
+ | |-- LAMP_Assay.py # load_alignment, clean_alignment, compute_conservation, gc, bad_run,
184
+ | | # mismatch_cost, primers_ok, scan_primers, primer_species_coverage,
185
+ | | # filter_primers_by_species, species_coverage, primers_clash,
186
+ | | # build_clash_map, amplicon_heuristic, detect_lamp_sets, evaluate_primer3,
187
+ | | # vienna_fold_dna, validate_primer_vienna, validate_lamp_set_vienna,
188
+ | | # primer_basic_score, primer_thermo_score, primer_struct_score,
189
+ | | # primer_conservation_score, amplicon_score, lamp_score, rtlamp_score,
190
+ | | # suggest_degenerate, analyze_failure_modes, mutate_base, perturb_primer,
191
+ | | # perturbation_analysis, build_robustness_matrix,
192
+ | | # compute_perturbation_robustness_scores, debug_no_matches, main
193
+ | |-- LAMP-hits.py # blast_sequences, biologically_meaningful
194
+ | |-- pertubation_final.py # best_mismatch_score,
195
+ | |-- primer_optimise.py # load_alignment, clean_alignment, gc, bad_run, rc, mismatch_cost,
196
+ | # primer_species_coverage, thermo_score, primer_ok, optimise_primer,
197
+ | # vienna_fold_dna, vienna_validate_set, mutate_base, perturb_primer,
198
+ | # perturbation_analysis, compute_robustness_score, build_full_lset, main
199
+ |
200
+ |-- simulations/
201
+ | |-- curve_fit.py # fit_standard_curve, copies_from_Tt
202
+ | |-- dye.py # color_pr_from_copies, delta_rgb, parameters: PR_BASELINE
203
+ | |-- model_rtlamp.py # best_match_mismatches, compute_hairpin, compute_homodimer,
204
+ | | # compute_heterodimer, has_3prime_dimer, compute_primer_features,
205
+ | | # fraction_sequestered, fraction_free, binding_efficiency,
206
+ | | # dimer_sink_factor, lamp_tm_score, lamp_primer_biophysical_score,
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+ | | # rt_lamp_rate, simulate_rt_qlamp
208
+ | |-- sim_curve.py # simulate_quant_curve_pr, parameters: QUANT_CONC
209
+ |
210
+ |-- species/
211
+ | |-- accession.py # extract_accession, extract_accessions_from_csv
212
+ | |-- ncbi_lookup.py # accession_to_gene_id, get_species_from_accession
213
+ | |-- table.py # write_species_lookup
214
+ |
215
+ |-- thermodynamics/
216
+ | |-- fold_rna.py # fold_rna
217
+ | |-- primer_access.py # binding_accessibility
218
+ | |-- primer3_eval.py # evaluate_primer3
219
+ | |-- scoring.py # thermo_score
220
+ | |-- simple_thermo.py # thermo
221
+ | |-- vienna_eval.py # vienna_fold_dna, validate_primer_vienna, validate_lamp_set_vienna
222
+ |
223
+ |-- utils/
224
+ | |-- build_primers.py # build_BIP, build_FIP
225
+ | |-- gc_content.py # gc_content
226
+ | |-- gene_primer.py # load_gene_primer_csv
227
+ | |-- load_seq.py # load_primers_csv, load_fasta
228
+ | |-- seq.py # gc, bad_run, rc
229
+ | |-- valid_csv_write.py # write_outputs
230
+ |
231
+ |-- __init__.py
232
+ |-- LICENSE # open access code - must cite
233
+ |-- README.md
234
+ ```
@@ -0,0 +1,8 @@
1
+ LICENSE
2
+ README.md
3
+ pyproject.toml
4
+ wildlamp.egg-info/PKG-INFO
5
+ wildlamp.egg-info/SOURCES.txt
6
+ wildlamp.egg-info/dependency_links.txt
7
+ wildlamp.egg-info/requires.txt
8
+ wildlamp.egg-info/top_level.txt
@@ -0,0 +1,13 @@
1
+ biopython>=1.80
2
+ numpy>=1.23
3
+ pandas>=1.5
4
+ matplotlib>=3.6
5
+ requests>=2.28
6
+ primer3-py>=0.7
7
+ viennarna>=2.6
8
+
9
+ [dev]
10
+ pytest
11
+ black
12
+ ruff
13
+ mypy