23andMe / bonsaitreeLinks
☆17Updated 10 months ago
Alternatives and similar repositories for bonsaitree
Users that are interested in bonsaitree are comparing it to the libraries listed below
Sorting:
- Lossless VCF compression☆20Updated 3 years ago
- ☆11Updated 2 years ago
- Evaluation of phasing performance☆23Updated 7 years ago
- Ximmer is a system for CNV calling on exome and targeted genomic sequencing☆19Updated 3 weeks ago
- FermiKit small variant calls for public SGDP samples☆17Updated 8 years ago
- Recommended Graphtyper pipelines☆14Updated 4 years ago
- PopSTR - A Population based microsatellite genotyper☆33Updated last year
- Population-scale detection of novel sequence insertions☆27Updated 3 years ago
- Simultaneous detection of SNPs and Indels using a 16-genotype probabilistic model☆27Updated last year
- Reducing reference bias using multiple population reference genomes☆32Updated last year
- Unfazed by genomic variant phasing☆27Updated last year
- Structural Variation breakpoint discovery via adaptive learning☆16Updated 2 years ago
- Kinship (genetic relatedness) using GBS (genotyping-by-sequencing) with Depth adjustment☆21Updated last month
- Expectation-Maximization algorithm for Allele-Specific Expression☆21Updated 2 years ago
- Population-wide Deletion Calling☆35Updated 4 months ago
- A small repo for storing the code for making the files and html for CCRs.☆22Updated 5 years ago
- Graphite - Graph-based variant adjudication☆28Updated 4 years ago
- ☆21Updated last week
- Samwell: a python package for using genomic files... well☆20Updated 3 years ago
- Preprocessing paired-end reads produced with experiment-specific protocols☆32Updated 7 years ago
- Fast-SG: An alignment-free algorithm for ultrafast scaffolding graph construction from short or long reads.☆22Updated 7 years ago
- Work for the tree sequence inference paper.☆23Updated 4 years ago
- Pan gGnome Viewer☆10Updated last month
- Identifying, understanding, and correcting technical biases on the sex chromosomes in next-generation sequencing data☆23Updated 6 years ago
- Bam Read Index - Extract alignments from a bam file by readname☆27Updated last year
- Mapping-free variant caller for short-read Illumina data☆19Updated 5 years ago
- Python package and routines for merging VCF files☆29Updated 4 years ago
- program for haplotype phasing from sequence reads and related tools☆25Updated 6 years ago
- sort genomic data☆36Updated 5 years ago
- VariantStore: A Large-Scale Genomic Variant Search Index☆39Updated 4 years ago