Mercurial > repos > greg > pima_report
changeset 25:4986a7fb2145 draft
Uploaded
author | greg |
---|---|
date | Thu, 20 Apr 2023 18:47:01 +0000 |
parents | 803e5965ed20 |
children | 46edd7435555 |
files | pima_report.py pima_report.xml |
diffstat | 2 files changed, 8 insertions(+), 3 deletions(-) [+] |
line wrap: on
line diff
--- a/pima_report.py Thu Apr 20 18:10:58 2023 +0000 +++ b/pima_report.py Thu Apr 20 18:47:01 2023 +0000 @@ -542,7 +542,7 @@ contig_title = 'Alignment to %s' % contig self.doc.new_line() self.doc.new_header(level=3, title=contig_title) - self.doc.new_line('Blue indicates aligned sequences (to the reference) and yellow indicates missing sequences') + self.doc.new_line('Blue color indicates query sequences aligned to the reference sequence, which is shown in yellow') self.doc.new_line(self.doc.new_inline_image(text='contig_title', path=os.path.abspath(circos_file))) self.doc.new_line('<div style="page-break-after: always;"></div>') self.doc.new_line() @@ -714,7 +714,7 @@ amr_deletions = amr_deletions.loc[amr_deletions['type'].isin(['large-deletion', 'any']), :] self.doc.new_line() self.doc.new_header(level=2, title=self.large_indel_title) - self.doc.new_line('This section is informative only when your idolates were identified as *Bacillus anthracis* strains') + self.doc.new_line('This section is informative only when your isolates were identified as *Bacillus anthracis* strains') for genome in ['Reference insertions', 'Query insertions']: genome_indels = large_indels[genome].copy() self.doc.new_line()
--- a/pima_report.xml Thu Apr 20 18:10:58 2023 +0000 +++ b/pima_report.xml Thu Apr 20 18:47:01 2023 +0000 @@ -7,7 +7,11 @@ <command detect_errors="exit_code"><![CDATA[ #import re -#set analysis_name = re.sub('[^\s\w\-]', '_', str($fastq_file.element_identifier)) +#if str($read_type) == 'ont': + #set analysis_name = re.sub('[^\s\w\-]', '_', str($fastq_file.element_identifier)) +#else: + #set analysis_name = re.sub('[^\s\w\-]', '_', str($extracted_fastq_file.element_identifier)) +#end if #set assembly_name = re.sub('[^\s\w\-]', '_', str($assembly_fasta_file.element_identifier)) #if str($bedtools_complementbed_file) not in ['None', '']: @@ -137,6 +141,7 @@ <param name="contig_coverage_file" type="data" format="tabular,tsv" label="Contig coverage tabular file"/> <param name="dnadiff_snps_file" type="data" format="tabular" label="DNAdiff snps tabular file"/> <param name="errors_file" type="data" format="txt" label="AMR mutation regions error txt file"/> + <param name="extracted_fastq_file" type="data" format="fastqsanger,fastqsanger.gz" optional="true" label="Fastq sample file extracted from a paired collection" help="Used only with Illumina paired reads, leave blank to ignore"/> <param name="fastq_file" type="data" format="fastqsanger,fastqsanger.gz" label="Fastq sample file"/> <param name="features_bed" format="bed" type="data_collection" collection_type="list" label="Collection of best feature hits BED files"/> <param name="features_png" format="png" type="data_collection" collection_type="list" label="Collection of best feature hits PNG files"/>