apscale-gui 3.2.1__tar.gz → 3.2.2__tar.gz

This diff represents the content of publicly available package versions that have been released to one of the supported registries. The information contained in this diff is provided for informational purposes only and reflects changes between package versions as they appear in their respective public registries.
@@ -1,6 +1,6 @@
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  Metadata-Version: 2.4
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  Name: apscale_gui
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- Version: 3.2.1
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+ Version: 3.2.2
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  Summary: Advanced Pipeline for Simple yet Comprehensive AnaLysEs of DNA metabarcoding data - Graphical User Interface
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  Home-page: https://github.com/TillMacher/apscale_gui
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  Author: Till-Hendrik Macher
@@ -942,6 +942,8 @@ def main():
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  if st.session_state["P5 Primer (5' - 3')"] == '' or st.session_state["P7 Primer (5' - 3')"] == '' or st.session_state['min length'] == '' or st.session_state['max length'] =='':
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  st.error('Please fill out all required fields!')
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+ elif float(st.session_state["sequence group threshold"]) >= 1:
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+ st.error('Please choose a sequence group threshold > 1.\n\nESVs are generated seperately!')
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  else:
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  if st.session_state['run_apscale_mode'] == 'Run apscale (basic mode)':
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  st.info('The "Basic mode" mode skips "Replicate merging" and "NC removal".')
@@ -1040,19 +1042,16 @@ def main():
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  subprocess.Popen(cmd, creationflags=subprocess.DETACHED_PROCESS | subprocess.CREATE_NEW_PROCESS_GROUP)
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  st.success("APSCALE analysis module started — it will open in a new browser tab.")
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- with st.expander("🧩 TaxonTableTools Table Conversion", expanded=False):
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+ with st.expander("🧩 TaxonTableTools2", expanded=False):
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  st.write(
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- "Combine your read and taxonomy tables into a single, merged table. "
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- "This format is fully compatible with TaxonTableTools for downstream analyses "
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- "and provides a more convenient structure for working with your data."
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- )
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- available_read_tables = {Path(i).name: Path(i) for i in glob.glob(str(project_folder / '11_read_table' / 'data' / '*_read_table_*.xlsx'))}
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- available_taxonomy_tables = {Path(i).name: Path(i) for i in glob.glob(str(project_folder / '11_read_table' / 'data' / 'blastn_*' / 'blastn_*.xlsx'))}
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- st.selectbox(label='Read table', key='TTT_read_table', options=list(available_read_tables.keys()))
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- st.selectbox(label='Taxonomy table', key='TTT_taxonomy_table', options=list(available_taxonomy_tables.keys()))
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-
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- if st.button('Merge tables'):
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- merge_tables(available_read_tables[st.session_state['TTT_read_table']], available_taxonomy_tables[st.session_state['TTT_taxonomy_table']])
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+ "Combine your read and taxonomy tables into a single, merged table for TaxonTableTools2.\n\n"
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+ "TaxonTableTools2 (TTT) is an easy-to-use graphical software designed for the analysis"
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+ "and visualization of DNA metabarcoding data. It enables biologists and researchers"
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+ "without bioinformatics experience to explore taxonomic datasets quickly, reproducibly,"
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+ "and interactively through a modern graphical user interface."
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+ )
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+ if st.button('Learn More'):
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+ webbrowser.open("https://github.com/TillMacher/TaxonTableTools2")
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  ############################################################################################################
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  st.markdown("---")
@@ -1,6 +1,6 @@
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  Metadata-Version: 2.4
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  Name: apscale_gui
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- Version: 3.2.1
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+ Version: 3.2.2
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  Summary: Advanced Pipeline for Simple yet Comprehensive AnaLysEs of DNA metabarcoding data - Graphical User Interface
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  Home-page: https://github.com/TillMacher/apscale_gui
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  Author: Till-Hendrik Macher
@@ -5,7 +5,7 @@ with open("README.md", "r") as fh:
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  setuptools.setup(
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  name="apscale_gui",
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- version="3.2.1",
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+ version="3.2.2",
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  author="Till-Hendrik Macher",
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  author_email="macher@uni-trier.de",
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  description="Advanced Pipeline for Simple yet Comprehensive AnaLysEs of DNA metabarcoding data - Graphical User Interface",
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