☆16Jun 12, 2023Updated 2 years ago
Alternatives and similar repositories for PDF-tools
Users that are interested in PDF-tools are comparing it to the libraries listed below
Sorting:
- Classifier of pathogenic non-coding variants in Mendelian diseases☆10Feb 6, 2020Updated 6 years ago
- ☆12Apr 26, 2020Updated 5 years ago
- A local realigner around InDels for MethylSeq data☆12Apr 28, 2016Updated 9 years ago
- A protocol to estimate global ancestry starting from raw Illumina data☆11Oct 16, 2019Updated 6 years ago
- Fast, accurate and simple to use command line tool for variant detection in NGS data.☆12Sep 3, 2019Updated 6 years ago
- visualization tools for exon/junction coverage☆11Dec 30, 2019Updated 6 years ago
- Translocator: local realignment and global remapping enabling accurate translocation detection using single-molecule sequencing long read…☆12Jan 22, 2020Updated 6 years ago
- Pipeline in place at the UGI for DNA level analysis☆11Aug 29, 2016Updated 9 years ago
- Divine: Prioritizing Genes for Rare Mendelian Disease in Whole Exome Sequencing Data☆13Apr 18, 2019Updated 6 years ago
- ☆13Apr 18, 2022Updated 3 years ago
- Pan gGnome Viewer☆10Jul 10, 2025Updated 7 months ago
- Naive PCA for genotype data☆10Jul 27, 2016Updated 9 years ago
- Header-only, gzread-like reader for gzip, bz2, and xz.☆11Aug 8, 2018Updated 7 years ago
- A nextflow pipeline for calling and annotating small germline variants from short DNA reads for WES and WGS data☆13Updated this week
- CardiacProfileR: An R package for extraction and visualisation of heart rate profiles from wearable fitness trackers☆12Jun 10, 2018Updated 7 years ago
- Code to reproduce "Detecting liver cancer using cell-free DNA fragmentomes☆11Nov 18, 2022Updated 3 years ago
- WGS Pipeline☆13Jan 19, 2018Updated 8 years ago
- A tool to examine duplicate read characteristics in a BAM file☆12Dec 8, 2017Updated 8 years ago
- Rails application for storing and parsing clinical exome VCF files. Gene annotations can be retrieved via Biomart integration from Ensemb…☆10May 7, 2017Updated 8 years ago
- ☆11Dec 9, 2022Updated 3 years ago
- Open Targets Genetics UI☆15Jan 31, 2025Updated last year
- Interactive table from gemini output☆10Mar 5, 2019Updated 7 years ago
- Algorithms that work on generic C arrays☆11Feb 13, 2017Updated 9 years ago
- A tool to analyze telomeric reads from WGS or telobait-capture long-read sequencing data☆10Oct 1, 2024Updated last year
- Run-length compressed BWT with LZ77 sampled suffix array☆10Apr 25, 2022Updated 3 years ago
- A fork of the project Excavator2 from sourceforge.☆10Jun 29, 2017Updated 8 years ago
- Pipeline for generating RNAseq-based cancer patient reports☆11Updated this week
- Web application for clinical pharmacogenomic interpretation☆10Mar 3, 2017Updated 9 years ago
- ☆11Jun 14, 2023Updated 2 years ago
- Directly create a bigwig file with signal derived from a sorted and indexed bam file.☆11Jul 7, 2017Updated 8 years ago
- NIPT-human-genetics is a semi-automated workflow designed for the analysis of large-scale ultra-low-pass non-invasive prenatal test (NIPT…☆13Sep 22, 2025Updated 5 months ago
- A nextflow pipeline for calling exome CNVs☆13Feb 24, 2026Updated last week
- A varitation graph tool☆10Dec 23, 2019Updated 6 years ago
- A fast and efficient short read mapper☆13Nov 7, 2021Updated 4 years ago
- Add functional variant annotation to MAF file☆11Nov 20, 2024Updated last year
- Software for creating and comparing genome fingerprints.☆11Jun 30, 2024Updated last year
- Code used to process and analyze structural variants and short tandem repeat variants profiled in 719 deeply sequenced whole genomes as p…☆11Jun 25, 2019Updated 6 years ago
- File parsing and writing code for Ensembl☆10Jan 7, 2026Updated last month
- ☆11Apr 3, 2023Updated 2 years ago