Welcome to Lithuania Basketball Match Predictions
  Embark on a thrilling journey into the world of Lithuania basketball with our expert match predictions. As a dedicated platform, we provide daily updates, offering you the latest insights and betting forecasts for all upcoming games. Whether you're a seasoned sports enthusiast or new to the excitement of basketball, our content is designed to keep you informed and ahead of the game.
  
  Why Choose Our Expert Predictions?
  Our predictions are crafted by seasoned analysts who meticulously analyze team performances, player statistics, and historical data. We aim to give you an edge in your betting strategies by providing comprehensive insights that go beyond the surface.
  Understanding the Lithuanian Basketball Landscape
  Lithuania's basketball scene is vibrant and competitive, with a rich history that has produced some of Europe's finest players. The Lithuanian Basketball League (LKL) is the pinnacle of domestic basketball, featuring intense rivalries and high-caliber talent.
  
    - Historical Context: Lithuania has a storied tradition in basketball, often referred to as "The Land of Champions." The country has produced legendary players like Arvydas Sabonis and Šarūnas Marčiulionis.
- Current Competitions: The LKL is renowned for its competitive nature, often serving as a proving ground for young talent before they make their mark on international stages like the NBA.
- Key Teams: Teams such as Žalgiris Kaunas and Rytas Vilnius are household names, known for their passionate fan bases and consistent performances.
Daily Match Updates
  Stay updated with our daily match reports that cover every angle of the game. From pre-match analysis to post-game reviews, we ensure you have all the information you need to make informed decisions.
  
    - Pre-Match Analysis: Get insights into team form, head-to-head records, and key player matchups.
- In-Game Updates: Follow live commentary and updates as the action unfolds on the court.
- Post-Match Review: Understand what went right or wrong through detailed analyses and expert opinions.
Betting Predictions: A Strategic Edge
  Betting on basketball can be both exciting and lucrative if approached with the right strategy. Our expert predictions are designed to guide you through the complexities of sports betting, offering tips and insights to enhance your chances of success.
  
    - Odds Analysis: Learn how to interpret betting odds and understand what they mean for your potential winnings.
- Prediction Models: Discover our proprietary prediction models that use advanced algorithms to forecast match outcomes.
- Betting Tips: Receive expert tips on value bets, underdogs, and over/under markets to maximize your returns.
Key Factors Influencing Match Outcomes
  Several factors can influence the outcome of a basketball match. Understanding these elements can provide you with a deeper insight into how games might unfold.
  
    - Team Form: Recent performances can be a strong indicator of a team's current strength and momentum.
- Injury Reports: Player availability due to injuries can significantly impact team dynamics and strategies.
- Historical Performance: Past encounters between teams can offer valuable insights into potential game plans and outcomes.
- Home Advantage: Playing at home often provides teams with a psychological edge due to familiar surroundings and supportive crowds.
Detailed Match Previews
  Before each match day, we provide detailed previews that cover all aspects of the upcoming games. These previews are designed to give you a comprehensive understanding of what to expect.
  
    - Squad News: Updates on team line-ups, including any last-minute changes or tactical adjustments.
- Tactical Analysis: Insights into potential strategies teams might employ based on their strengths and weaknesses.
- Pitch Conditions: Information on venue conditions that could affect gameplay, such as court surface or lighting.
The Role of Key Players
  In basketball, individual performances can often be the difference between victory and defeat. We highlight key players whose performances could sway the outcome of matches.
  
    - All-Star Performers: Players known for their consistent high-level performances across seasons.
- Rising Stars: Young talents making a name for themselves in the league with standout skills and potential.
- Influential Veterans: Experienced players who bring leadership and composure under pressure.
Tactical Breakdowns
  Tactics play a crucial role in basketball matches. Our tactical breakdowns provide an in-depth look at how teams might approach each game strategically.
  
    - Opposition Analysis: Detailed examination of opponent tactics and how they might counteract them.
- Possession Strategies: Insights into how teams manage ball control and create scoring opportunities.
- Defensive Schemes: Understanding different defensive setups teams use to stifle their opponents' attacks.
The Importance of Fan Engagement
  Fan support can be a powerful motivator for teams. We explore how fan engagement influences team performance and atmosphere during matches.
  
    - Fan Presence: The impact of having a strong fan base present at games, boosting team morale.
- Social Media Influence: How teams interact with fans online can affect public perception and player motivation.
- Crowd Dynamics: The role of crowd noise and energy in creating an intimidating environment for visiting teams.
Betting Strategies: Maximizing Your Returns
kylecarlton/precise-gene<|file_sep|>/precisegenelib/coverage.py
#!/usr/bin/env python
from __future__ import print_function
import argparse
import os
import pysam
import sys
def parse_args():
	"""
	Parse command line arguments.
	"""
	parser = argparse.ArgumentParser(description="Count coverage in BAM files.")
	parser.add_argument("bam_file", help="BAM file")
	parser.add_argument("bed_file", help="BED file")
	parser.add_argument("--base_coverage", type=int,
		default=1,
		help="Base coverage threshold")
	parser.add_argument("--min_region_coverage", type=int,
		default=1,
		help="Minimum region coverage threshold")
	parser.add_argument("--max_region_coverage", type=int,
		default=sys.maxint,
		help="Maximum region coverage threshold")
	parser.add_argument("--min_mapq", type=int,
		default=0,
		help="Minimum mapping quality")
	parser.add_argument("--max_mapq", type=int,
		default=sys.maxint,
		help="Maximum mapping quality")
	parser.add_argument("--output_file",
		help="Output file")
	args = parser.parse_args()
	return args
def main():
	args = parse_args()
	bam_file = args.bam_file
	bed_file = args.bed_file
	base_coverage = args.base_coverage
	min_region_coverage = args.min_region_coverage
	max_region_coverage = args.max_region_coverage
	min_mapq = args.min_mapq
	max_mapq = args.max_mapq
	output_file = args.output_file
	if output_file:
		outf = open(output_file, "w")
	else:
		outf = sys.stdout
	bedfile = pysam.Tabixfile(bed_file)
	bamfile = pysam.Samfile(bam_file)
	for i in range(bedfile.nreferences):
		chrom = bamfile.getrname(i)
		for interval in bedfile.fetch(chrom):
			start_pos = int(interval[1])
			end_pos = int(interval[2])
			name = interval[3]
			coverage_counts = [0] * (end_pos - start_pos)
			for read in bamfile.fetch(chrom, start_pos, end_pos):
				if min_mapq <= read.mapq <= max_mapq:
					for pos in read.positions:
						if start_pos <= pos <= end_pos:
							base_cov_index = pos - start_pos
							if read.is_reverse:
								if read.is_paired:
									if read.mate_is_unmapped:
										continue
									else:
										pair_orientation = (read.is_reverse != read.mate_is_reverse)
								else:
									pair_orientation = False
							else:
								if read.is_paired:
									if read.mate_is_unmapped:
										continue
									else:
										pair_orientation = (read.is_reverse == read.mate_is_reverse)
								else:
									pair_orientation = False
							if base_cov_index >= len(coverage_counts):
								print("WARNING: Index out-of-bounds:", base_cov_index)
								continue
							if not pair_orientation:
								if read.is_duplicate or read.is_secondary or 
								   read.is_qcfail or read.is_unmapped or 
								   not read.is_proper_pair or 
								   not (base_coverage <= coverage_counts[base_cov_index] <= max_region_coverage):
									continue
							if coverage_counts[base_cov_index] >= max_region_coverage:
								continue
							coverage_counts[base_cov_index] +=1
			total_coverage_count = sum(coverage_counts)
			print(chrom + "t" + str(start_pos) + "t" + str(end_pos) + "t" + name + "t" + str(total_coverage_count), file=outf)
if __name__ == "__main__":
	main()
<|repo_name|>kylecarlton/precise-gene<|file_sep|>/scripts/download_data.sh
#!/bin/bash
# This script downloads data for running precise-gene.
# Directories.
data_dir=data # Directory containing data files.
gff3_dir=$data_dir/gff3 # Directory containing GFF3 files.
gtf_dir=$data_dir/gtf # Directory containing GTF files.
fa_dir=$data_dir/fa # Directory containing FASTA files.
bed_dir=$data_dir/bed # Directory containing BED files.
# Files.
gencode_v29_gff3=$gff3_dir/gencode.v29.annotation.gff3.gz # Gencode v29 GFF3 file.
gencode_v29_gtf=$gtf_dir/gencode.v29.annotation.gtf.gz # Gencode v29 GTF file.
hg38_ucsc_refseq_genome_fasta=$fa_dir/hg38_ucsc_refseq_genome.fa.gz # UCSC hg38 reference genome FASTA file.
hg38_ucsc_refseq_genome_fai=$fa_dir/hg38_ucsc_refseq_genome.fa.fai.gz # UCSC hg38 reference genome FASTA index file.
hg38_ucsc_refseq_genome_dict=$fa_dir/hg38_ucsc_refseq_genome.dict # UCSC hg38 reference genome dictionary file.
refgene_ucsc_hg38_bed12=$bed_dir/refGene_ucsc_hg38.bed12.gz # RefGene UCSC hg38 BED12 file.
# Create directories if needed.
mkdir -p $data_dir $gff3_dir $gtf_dir $fa_dir $bed_dir
# Download files if needed.
if [ ! -e $gencode_v29_gff3 ]; then
	wget ftp://ftp.ebi.ac.uk/pub/databases/gencode/Gencode_human/release_29/gencode.v29.annotation.gff3.gz -P $gff3_dir
fi
if [ ! -e $gencode_v29_gtf ]; then
	wget ftp://ftp.ebi.ac.uk/pub/databases/gencode/Gencode_human/release_29/gencode.v29.annotation.gtf.gz -P $gtf_dir
fi
if [ ! -e $hg38_ucsc_refseq_genome_fasta ]; then
	wget http://hgdownload.cse.ucsc.edu/goldenPath/hg38/bigZips/hg38.fa.gz -P $fa_dir && mv $fa_dir/hg38.fa.gz $fa_dir/hg38_ucsc_refseq_genome.fa.gz 
fi
if [ ! -e $hg38_ucsc_refseq_genome_fai ]; then
	wget http://hgdownload.cse.ucsc.edu/goldenPath/hg38/bigZips/hg38.fa.fai.gz -P $fa_dir && mv $fa_dir/hg38.fa.fai.gz $fa_dir/hg38_ucsc_refseq_genome.fa.fai.gz 
fi
if [ ! -e $hg38_ucsc_refseq_genome_dict ]; then
	wget http://hgdownload.cse.ucsc.edu/goldenPath/hg38/bigZips/hg38.dict -P $fa_dir && mv $fa_dir/hg38.dict $fa_dir/hg38_ucsc_refseq_genome.dict 
fi
if [ ! -e $refgene_ucsc_hg38_bed12 ]; then
	wget http://hgdownload.cse.ucsc.edu/goldenPath/hg38/database/refGene.txt.gz -P $bed_dir && zcat $bed_dir/refGene.txt.gz | awk '{printf "%st%dt%dt%st%dt%st%st%dt%d,%d,%d,%d,%d,%d,%d,%dn", $1,$2,$3,$4,$5,$6,$7,$8,$9,$10,$11,$12,$13,$14,$15}' | gzip >$bed_dir/refGene_ucsc_hg38.bed12.gz && rm $bed_dir/refGene.txt.gz 
fi<|repo_name|>kylecarlton/precise-gene<|file_sep|>/precisegenelib/utils.py
#!/usr/bin/env python
from __future__ import print_function
import sys
def log(message):
	print(message)
def fatal(message):
	sys.stderr.write(message)
	sys.exit(1)
<|repo_name|>kylecarlton/precise-gene<|file_sep|>/scripts/parse_chromosome_sizes.sh
#!/bin/bash 
# This script parses chromosome sizes from FASTA index files.
# Directories.
data_in=$1 # Input directory containing FASTA index files.
data_out=$2 # Output directory containing chromosome sizes files.
# Create output directory if needed.
mkdir -p $data_out 
for fai_file in `ls ${data_in}/*.fai`; do 
	chrom_sizes_file=${data_out}/`basename ${fai_file} .fai`.chrom.sizes 
	echo "Parsing chromosome sizes from ${fai_file}..."
	zcat ${fai_file} | awk '{print $1"t"$2}' >${chrom_sizes_file}
done<|repo_name|>kylecarlton/precise-gene<|file_sep|>/scripts/parse_chromosome_lengths.py
#!/usr/bin/env python
"""
This script parses chromosome lengths from FASTA index files.
Usage: ./parse_chromosome_lengths.py input_directory output_directory
"""
from __future__ import print_function
import argparse
import os
def parse_args():
	"""
	Parse command line arguments.
	"""
	parser = argparse.ArgumentParser(description="Parse chromosome lengths from FASTA index files.")
	parser.add_argument("input_directory", help="Input directory containing FASTA index files.")
	parser.add_argument("output_directory", help="Output directory containing chromosome length files.")
	args = parser.parse_args()
	return args
def main():
	args = parse_args()
	input_directory = args.input_directory 
	output_directory = args.output_directory 
	for fai_filename in os.listdir(input_directory):
		fai_filename_path_and_ext=os.path.join(input_directory,fai_filename)
		fai_filename_path=os.path.splitext(fai_filename_path_and_ext)[0]
		
		chrom_length_filename=fai_filename_path+".chrom.lengths"
		
		with open(fai_filename_path_and_ext,"r") as fai_handle:
			with open(os.path.join(output_directory,chrom_length_filename),"w") as chrom_length_handle:
				for line in fai_handle.readlines():
					line=line.strip()
					tokens=line.split("t")
					chrom=tokens[0]
					length=int(tokens[1])
					print(chrom+"t"+str(length),file=chrom_length_handle)
if __name__ == "__main__":
	main()<|repo_name|>kylecarlton/precise-gene<|file_sep|>/README.md
# Precise Gene
## Description
Precise Gene is a software package for discovering precise gene boundaries using RNA-seq data.
## Installation Instructions 
### Requirements 
- Python (tested with version >=3.6).
- Java (tested with version >=1.8).
- GNU parallel (tested with version >=20150522).
### Install Precise Gene 
#### Clone Repository 
Clone this repository using `git clone https://github.com/kylecarlton/precise-gene.git`.
#### Install Python Dependencies 
Run `pip install -r requirements.txt` from within this repository.
#### Install STAR 
Download STAR from http://bioinformatics.mdanderson.org/public/software/star/index.html.
Unzip STAR into this repository.
#### Download Data Files 
Run `./scripts/download_data.sh` from within this repository. This will download necessary data files into `data`, `data/gff3`, `data/gtf`, `data/fa`, `data/bed`.
## Usage Instructions 
### Overview 
Precise Gene runs in three steps:
1. Mapping reads from RNA-seq experiments to reference genomes using STAR aligner.
   For example:
   
   ./scripts/run_star_mapping.sh 
       --star_executable=./STAR 
       --genomeDir=./STAR/genomes/Homo_sapiens 
       --read_files_in=reads_1.fq reads_2.fq 
       --outFileNamePrefix=star_output_prefix