sphinx fixed

src/python/ensembl/tools/anno/transcriptomic_annotation/star.py

@@ -63,6 +63,7 @@ def run_star(  # pylint:disable=too-many-branches
 ) -> None:
     """
     Run STAR alignment on list of short read data.
+    
         :param genome_file: Genome file path.
         :type genome_file: Path
         :param output_dir: Working directory path.
@@ -81,15 +82,11 @@ def run_star(  # pylint:disable=too-many-branches
         :type subsample_read_limit:int, default 100000000,
         :param subsample_percentage: Maximun percentage of reads to subsample.
         :type subsample_percentage: int, default 0.25,
-        :param sampling_via_read_limit: If True will subsample an input dataset of \
-            fastq files using --subsample_read_limit value.
+        :param sampling_via_read_limit: subsample fastq files using --subsample_read_limit.
         :type sampling_via_read_limit : boolean, False,
-        :param sampling_via_percentage: If True will subsample an input dataset of \
-            fastq files using --subsample_percentage value.
+        :param sampling_via_percentage: subsample fastq files using --subsample_percentage.
         :type sampling_via_percentage : boolean, False,
-        :param sampling_via_read_limit_percentage: If True will subsample an input dataset \
-            of fastq files using --subsample_read_limit and --subsample_percentage value; \
-            the lowest number of reads is taken.
+        :param sampling_via_read_limit_percentage: use max read limit and  percentage value.
         :type sampling_via_read_limit_percentage : boolean, False,
         :param num_threads: Number of available threads.
         :type num_threads: int, default 1