ScreenPro2 0.5.0__tar.gz → 0.6.1__tar.gz

{screenpro2-0.5.0 → screenpro2-0.6.1}/LICENSE

@@ -1,6 +1,6 @@
 MIT License
 
-Copyright (c) 2022-2024 ScreenPro2 Development Team.
+Copyright (c) 2022-2026 ScreenPro2 Development Team.
 All rights reserved.
 Gilbart Lab, UCSF / Arc Institute.
 Multi-Omics Tech Center, Arc Insititue.

{screenpro2-0.5.0 → screenpro2-0.6.1}/PKG-INFO

@@ -1,11 +1,12 @@
-Metadata-Version: 2.3
+Metadata-Version: 2.4
 Name: ScreenPro2
-Version: 0.5.0
+Version: 0.6.1
 Summary: Flexible analysis of high-content CRISPR screening
 License: MIT
+License-File: LICENSE
 Keywords: CRISPR,screening,bioinformatics
-Author: Abe Arab
-Author-email: abea@arcinstitute.org
+Author: Abolfazl Arab
+Author-email: abolfazl.arab@ucsf.edu
 Requires-Python: >=3.9
 Classifier: License :: OSI Approved :: MIT License
 Classifier: Programming Language :: Python :: 3
@@ -14,16 +15,18 @@ Classifier: Programming Language :: Python :: 3.10
 Classifier: Programming Language :: Python :: 3.11
 Classifier: Programming Language :: Python :: 3.12
 Classifier: Programming Language :: Python :: 3.13
+Classifier: Programming Language :: Python :: 3.14
 Project-URL: Homepage, https://github.com/ArcInstitute/ScreenPro2
 Project-URL: Repository, https://github.com/ArcInstitute/ScreenPro2
 Description-Content-Type: text/markdown
 
 [![website](https://img.shields.io/badge/website-live-brightgreen)](https://arcinstitute.org/tools/screenpro2)
+[![DOI](https://zenodo.org/badge/DOI/10.5281/zenodo.18807934.svg)](https://doi.org/10.5281/zenodo.18807934)
 [![PyPI version](https://badge.fury.io/py/ScreenPro2.svg)](https://badge.fury.io/py/ScreenPro2)
 [![Documentation Status](https://readthedocs.org/projects/screenpro2/badge/?version=latest)](https://screenpro2.readthedocs.io/en/latest/?version=latest)
 [![Downloads](https://static.pepy.tech/badge/screenpro2)](https://pepy.tech/project/screenpro2)
 [![Downloads](https://static.pepy.tech/badge/screenpro2/month)](https://pepy.tech/project/screenpro2)
-[![CodeQL](https://github.com/ArcInstitute/ScreenPro2/actions/workflows/github-code-scanning/codeql/badge.svg)](https://github.com/ArcInstitute/ScreenPro2/actions/workflows/github-code-scanning/codeql)
+
 # ScreenPro2
 
 ## Introduction

{screenpro2-0.5.0 → screenpro2-0.6.1}/README.md

@@ -1,9 +1,10 @@
 [![website](https://img.shields.io/badge/website-live-brightgreen)](https://arcinstitute.org/tools/screenpro2)
+[![DOI](https://zenodo.org/badge/DOI/10.5281/zenodo.18807934.svg)](https://doi.org/10.5281/zenodo.18807934)
 [![PyPI version](https://badge.fury.io/py/ScreenPro2.svg)](https://badge.fury.io/py/ScreenPro2)
 [![Documentation Status](https://readthedocs.org/projects/screenpro2/badge/?version=latest)](https://screenpro2.readthedocs.io/en/latest/?version=latest)
 [![Downloads](https://static.pepy.tech/badge/screenpro2)](https://pepy.tech/project/screenpro2)
 [![Downloads](https://static.pepy.tech/badge/screenpro2/month)](https://pepy.tech/project/screenpro2)
-[![CodeQL](https://github.com/ArcInstitute/ScreenPro2/actions/workflows/github-code-scanning/codeql/badge.svg)](https://github.com/ArcInstitute/ScreenPro2/actions/workflows/github-code-scanning/codeql)
+
 # ScreenPro2
 
 ## Introduction

{screenpro2-0.5.0 → screenpro2-0.6.1}/pyproject.toml

@@ -1,9 +1,10 @@
 [tool.poetry]
 name = "ScreenPro2"
-version = "0.5.0"
 description = "Flexible analysis of high-content CRISPR screening"
+version = "0.6.1"
 authors = [
-    "Abe Arab <abea@arcinstitute.org>"
+	"Abolfazl Arab <abolfazl.arab@ucsf.edu>",
+	"Nick Youngblut <nick.youngblut@arcinstitute.org>",
 ]
 license = "MIT"
 readme = "README.md"
@@ -14,6 +15,7 @@ packages = [
 	{ include = "screenpro" },
 	{ include = "pyproject.toml" },
 ]
+dynamic = ["version"]
 
 [tool.poetry.dependencies]
 python = ">=3.9"
@@ -25,6 +27,9 @@ screenpro = "screenpro.main:main"
 pytest = "*"
 tomli = "*"
 
+[tool.poetry-dynamic-versioning]
+enable = true
+
 [build-system]
 requires = ["poetry-core>=1.0.0", "poetry-dynamic-versioning>=1.0.0,<2.0.0"]
-build-backend = "poetry_dynamic_versioning.backend"
+build-backend = "poetry.core.masonry.api"

{screenpro2-0.5.0 → screenpro2-0.6.1}/screenpro/__init__.py

@@ -29,3 +29,21 @@ from . import dashboard
 from .ngs import GuideCounter
 from .assays import PooledScreens, GImaps
 from .dashboard import DrugScreenDashboard
+
+
+def _get_version():
+
+    import os
+
+    pyproject_path = os.path.join(os.path.dirname(__file__), "..", "pyproject.toml")
+
+    with open(pyproject_path, "r") as pyproject_file:
+        for line in pyproject_file.readlines():
+            if "version" in line:
+                return line.split("=")[1].strip().strip('"')
+
+
+try:
+    __version__ = _get_version()
+except Exception:
+    __version__ = "Unknown"

{screenpro2-0.5.0 → screenpro2-0.6.1}/screenpro/assays/__init__.py

@@ -71,8 +71,8 @@ class PooledScreens(object):
         growth_factors = []
         # calculate growth factor for gamma, tau, or rho score per replicates
         for replicate in adat.obs.replicate.unique():
-            db_untreated = adat.obs.query(f'condition == "{untreated}" & replicate == {str(replicate)}')[db_rate_col][0]
-            db_treated = adat.obs.query(f'condition == "{treated}" & replicate == {str(replicate)}')[db_rate_col][0]
+            db_untreated = adat.obs.query(f'condition == "{untreated}" & replicate == {str(replicate)}')[db_rate_col].iloc[0]
+            db_treated = adat.obs.query(f'condition == "{treated}" & replicate == {str(replicate)}')[db_rate_col].iloc[0]
 
             growth_factors.append(('gamma', db_untreated, replicate, f'gamma_replicate_{replicate}'))
             growth_factors.append(('tau', db_treated, replicate, f'tau_replicate_{replicate}'))

{screenpro2-0.5.0 → screenpro2-0.6.1}/screenpro/ngs/cas9.py

@@ -154,10 +154,9 @@ def map_to_library_single_guide(df_count, library, return_type='all', verbose=Fa
         )
 
     if verbose:
-        print("% mapped reads",
-            100 * \
-            res_map.to_pandas()['count'].fillna(0).sum() / \
-            int(res.select(pl.sum("count")).to_pandas()['count'])
+        print(
+            "% mapped reads",
+            100 * res_map['count'].sum() / res["count"].sum()
         )
     
     if return_type == 'unmapped':
@@ -221,8 +220,8 @@ def map_to_library_dual_guide(df_count, library, get_recombinant=False, return_t
     if verbose:
         print("% mapped reads",
             100 * \
-            res_map.to_pandas()['count'].fillna(0).sum() / \
-            int(res.select(pl.sum("count")).to_pandas()['count'])
+            res_map['count'].sum() / \
+            res["count"].sum()
         )
     
     if get_recombinant:
@@ -230,8 +229,8 @@ def map_to_library_dual_guide(df_count, library, get_recombinant=False, return_t
         if verbose:
             print("% unmapped reads",
                 100 * \
-                res_unmap.to_pandas()['count'].fillna(0).sum() / \
-                int(res.select(pl.sum("count")).to_pandas()['count'])
+                res_unmap['count'].sum() / \
+                res["count"].sum()
             )
         
         sgRNA_table = pd.concat([
@@ -253,8 +252,8 @@ def map_to_library_dual_guide(df_count, library, get_recombinant=False, return_t
         if verbose:
             print("% fully remapped recombination events",
                 100 * \
-                res_recomb_events.drop_nulls().to_pandas()['count'].fillna(0).sum() / \
-                int(res.select(pl.sum("count")).to_pandas()['count'])
+                res_recomb_events.drop_nulls()['count'].sum() / \
+                res['count'].sum()
             )
     
     if return_type == 'unmapped':