Collection of scripts used in the Cassava Genomics Project
| Script | Version | Source | Cite |
|---|---|---|---|
| clean_genomic_fasta.py: Clean contig identifiers to avoid incompatibility issues | 0.15 | https://github.com/bpucker/GenomeAssembly/ | 10.1101/2023.06.27.546741 |
| contig_stats.py: Calculate contig statistics | 1.31 | https://github.com/bpucker/script_collection/ | 10.1371/journal.pone.0164321 |
| genetic_map_to_fasta.py: Create input file for ALLMAPS merge command by mapping genetic markers to assembly contigs | 0.2 | - | /10.1101/2024.09.30.615795 |
| cov_plot.py: Create assembly coverage plot from coverage file. | 0.2 | https://github.com/bpucker/At7 | 10.1371/journal.pone.0164321 |
| coverage_te_plot.py: Adjusted to create a coverage plot including density of TE repeats for M. esculenta. | 0.5 | - | 10.1371/journal.pone.0164321 |
| RNAseq_cov_analysis.py: Analyse coverage of predicted polypeptide sequences by RNAseq data | 0.1 | https://github.com/bpucker/GenomeAssembly/ | 10.1101/2023.06.27.546741 |
| TE_repeat_analysis.R: Analyse repeat density of EDTA results | 0.1 | - | 10.1038/s41597-023-02800-0 |
python genetic_map_to_fasta.py \
--map <FULL_PATH_TO_GENETIC_MAP_FILE> \
--contigs <FULL_PATH_TO_CONTIGS_FILE>
--output <BASE_PATH_TO_OUTPUT_FILE>
[--sim <MINIMUM_SIMILARITY_BEST_HIT]
[--score <MINIMUM_SCORE_BEST_HIT]
Mapping of genetic markers (--map) to assembly contigs (--contigs). Genetic markers are expected in the format of the composite genetic map from Manihot esculenta Crantz by the ICGMC (File S2, https://doi.org/10.1534/g3.114.015008).
Input:
--map: genetic markers--fasta: FASTA file containing assembly contigs--output: Base path to output files (without extension)
Output:
<output>.fasta: FASTA file containing marker sequences<output>_blastn_marker_contig_mapping.txt: BLASTN output<output>_mapped_contigs.csv: Mapped markers, compatible with ALLMAPS merge command
python coverage_te_plot.py \
--coverage_file <FULL_PATH_TO_COVERAGE_FILE> \
--te_file <FULL_PATH_TO_TE_FILE> \
--out <FULL_PATH_TO_OUTPUT_FILE> \
--cov <AVERAGE_COVERAGE>
[--res <RESOLUTION, WINDOW_SIZE_FOR_COVERAGE_CALCULATION> 1000]
[--sat <SATURATION, CUTOFF_FOR_MAX_COVERAGE_VALUE> 100.0]
[--num_contigs <NUMBER_OF_CONTIGS_TO_PLOT> 18]
[--max_cov <MAXIMUM_COVERAGE 600]
[--max_chromosome <MAXIMUM_CHROMOSOME_SIZE_BP 55000000]
Creates a coverage plot showing the average coverage in blocks of resolution size (--res). The maximum displayed coverage is defined by the saturation (--sat). Each chromosome is plotted separatly and the average coverage is marked by a red line. For each chromosome, a histogram is created showing the coverage distribution.
Input:
--coverage_file: Coverage file--te_file: Repeats TSV created with Circos genomicDensity function--cov: Average coverage--out: Base path to output files (without extension)
Output:
<out>.png: Coverage plot<out>_<contig>.png: Histogram of coverage for each contig/chromosome<out>_coverage_resolution<res>.tsv: Average coverage per block
Rscript TE_repeat_analysis.R \
--repeat_gff3 <FULL_PATH_TO_REPEAT_GFF3_FILE> \
--repeat_gff3_intact <FULL_PATH_TO_INTACT_REPEAT_GFF3_FILE> \
--gene_gff3 <FULL_PATH_TO_GENE_GFF3_FILE> \
--chr_length_A <FULL_PATH_TO_CHR_LENGTH_A_FILE> \
--chr_length_B <FULL_PATH_TO_CHR_LENGTH_B_FILE> \
--output_dir <FULL_PATH_TO_OUTPUT_DIRECTORY>
Analyzes EDTA annotation results by classifying repeats. A bar plot is generated to show the distribution of transposable element (TE) families across chromosomes for each haplophase separately. Additionally, a circos density plot is produced, displaying the genomic density of TE repeats, intact TE repeats, and predicted coding sequences. The inner track of the plot includes a rainfall (rainbow) plot that illustrates the minimal distance between neighboring repeats for each TE family.
Input:
--repeat_gff3: Path to repeat GFF3 file from EDTA results--repeat_gff3_intact: Path to intact repeat GFF3 file from EDTA results--gene_gff3: Path to GFF3 file annotating predicted coding sequences--chr_length_A: Path to TSV mapping chromosome IDs to chromosome length for haplophase A--chr_length_B: Path to TSV mapping chromosome IDs to chromosome length for haplophase B--output_dir: Directory for output files
Output:
<output_dir>/tables/TEs_barplot.png: Barplot showing distribution of TE families for each chromosome<output_dir>/tables/density_repeats_A.tsv: Density of repeats for haplophase A<output_dir>/tables/density_repeats_B.tsv: Density of repeats for haplophase B<output_dir>/plots/circos_genomic_density_A.png: Circos plot for haplophase A<output_dir>/plots/circos_genomic_density_B.png: Circos plot for haplophase B