sunnyeesl / BigLDLinks
☆21Updated 3 years ago
Alternatives and similar repositories for BigLD
Users that are interested in BigLD are comparing it to the libraries listed below
Sorting:
- Population-based detection of structural variation from High-Throughput Sequencing.☆33Updated 3 years ago
- Flexible Bayesian inference of mutational signatures☆37Updated 2 years ago
- Snakemake workflow for Illumina RNA-sequencing experiments - extract population genomic signals from RNA-Seq data☆18Updated 7 months ago
- A series of scripts to automate sequence workflows☆19Updated 6 months ago
- Tools for merging Tandem Repeat VCF files☆37Updated 7 months ago
- Unfazed by genomic variant phasing☆27Updated last year
- PopSTR - A Population based microsatellite genotyper☆33Updated 2 years ago
- Telomerecat: The telomere computational analysis tool☆21Updated 4 years ago
- Package Homepage: http://bioconductor.org/packages/devel/bioc/html/DRIMSeq.html Bug Reports: https://support.bioconductor.org/p/new/post/…☆11Updated 5 years ago
- R API for browsing, analyzing, and manipulating reference-aligned genome graphs in a GenomicRanges framework☆41Updated 3 weeks ago
- Large scale ancestry inference from PCA data☆23Updated 2 years ago
- Reducing reference bias using multiple population reference genomes☆34Updated last year
- Haplotype and population structure inference using neural networks.☆27Updated 11 months ago
- Preprocessing paired-end reads produced with experiment-specific protocols☆32Updated 7 years ago
- Runs a combination of tools to generate structural variant calls on short-read whole-genome sequencing data☆22Updated 4 years ago
- A flexible tool for the multi-resolution localization of causal variants across the genome, accounting for population structure.☆15Updated 3 years ago
- Splice junction analysis and filtering from BAM files☆42Updated 3 years ago
- Integrative analysis of complex structural variants☆22Updated 5 years ago
- Tools to gather evidence for structural variation via breakpoint detection.☆19Updated this week
- Functions to compare a SV call sets against a truth set.☆30Updated 5 months ago
- Simultaneous detection of SNPs and Indels using a 16-genotype probabilistic model☆27Updated last year
- Suite of tools for analysing off-target reads to find CNVs, homozygous regions, and shared haplotypes☆31Updated 3 months ago
- Genotyping of segregating mobile elements insertions☆19Updated 4 years ago
- novoBreak: local assembly for breakpoint detection in cancer genomes☆25Updated 7 years ago
- Teaching modules for Human Genome Variation Lab.☆20Updated 5 months ago
- ☆23Updated 11 months ago
- ☆29Updated 6 years ago
- Allele-specific copy number estimation with whole genome sequencing☆23Updated 2 years ago
- Immuological gene typing and annotation for genome assembly☆38Updated 8 months ago
- Abismal is a mapper of FASTQ bisulfite-converted short reads (between 50 and 1000 bases) to a FASTA reference genome.☆19Updated this week