FinaleToolkit 0.7.6

FinaleToolkit is a package and standalone program to extract fragmentation features of cell-free DNA from paired-end sequencing data.

‎ ‎ ‎FinaleToolkit

Table of Contents

1. About The Project
2. Installation
3. Usage
   • Functionality
   • Documentation
   • Compatible File Formats
   • Using Fragment Files
4. Contact
5. License

About The Project

FinaleToolkit (FragmentatIoN AnaLysis of cEll-free DNA Toolkit) is a package and standalone program to extract fragmentation features of cell-free DNA from paired-end sequencing data.

Citation

If you use FinaleToolkit in your research, please consider citing our paper:

Installation

You can install the package using pip.

$ pip install finaletoolkit

Usage

Functionality

FinaleToolkit has support for the following cell-free DNA fragmentation features:

• Fragment Length
• Coverage
• End Motifs
• Motif Diversity Score
• Windowed Protection Score
• DELFI
• Cleavage Profile

Documentation

Documentation for FinaleToolkit can be found here.

Compatible File Formats

FinaleToolkit is compatible with almost any paired-end sequence data:

• Binary Alignment Map (.bam) files with an associated index file (.bam.bai).
• Sequence Alignment Map (.sam) files.
• Compressed Reference-oriented Alignment Map (.cram) files.
• Fragment (.frag.gz) files with an associated tabix index file (.frag.gz.tbi).

Using Fragment Files

Fragment (.frag.gz) files are block-gzipped BED3+2 files with the following columns: chrom , start , stop , mapq , strand.

We encourage you to use our comprehensive database, FinaleDB, to access relevant fragment files. Learn more about FinaleDB here.

Contact

• James Li: [e-mail]
• Ravi Bandaru: [e-mail]
• Yaping Liu: [e-mail]

License

This project falls under an MIT license. See the included LICENSE file for details.