mebbert / Dark_and_Camouflaged_genesLinks
☆24Updated 6 months ago
Alternatives and similar repositories for Dark_and_Camouflaged_genes
Users that are interested in Dark_and_Camouflaged_genes are comparing it to the libraries listed below
Sorting:
- Multi-sample genome coverage viewer to observe large, coverage-based anomalies alongside annotations and sample metadata☆58Updated 3 years ago
- Samwell: a python package for using genomic files... well☆20Updated 3 years ago
- Population-wide Deletion Calling☆35Updated 7 months ago
- Structural variant (SV) analysis tools☆39Updated last year
- Functions to compare a SV call sets against a truth set.☆30Updated 5 months ago
- Pipeline for structural variant image curation and analysis.☆49Updated 4 years ago
- Reducing reference bias using multiple population reference genomes☆34Updated last year
- ☆29Updated 6 years ago
- Unfazed by genomic variant phasing☆27Updated last year
- Tools for merging Tandem Repeat VCF files☆37Updated 7 months ago
- Exploration of controlled loss of quality values for compressing CRAM files☆36Updated 2 years ago
- Suite of tools for analysing off-target reads to find CNVs, homozygous regions, and shared haplotypes☆31Updated 3 months ago
- Evaluation of phasing performance☆23Updated 7 years ago
- ☆35Updated 4 years ago
- Bam Read Index - Extract alignments from a bam file by readname☆28Updated last year
- Runs a combination of tools to generate structural variant calls on short-read whole-genome sequencing data☆22Updated 4 years ago
- Preprocessing paired-end reads produced with experiment-specific protocols☆32Updated 7 years ago
- Easy genomic regions for short-read variant calling☆45Updated 3 months ago
- MapCaller – An efficient and versatile approach for short-read alignment and variant detection in high-throughput sequenced genomes☆30Updated 4 years ago
- Exact Tandem Repeat Finder (not a TRF replacement)☆50Updated 6 years ago
- Structural Variant Prediction Viewer☆35Updated 8 years ago
- What is true, thank you, ernestly. A large variant benchmarking tool analogous to hap.py for small variants.☆34Updated 2 years ago
- Immuological gene typing and annotation for genome assembly☆38Updated 8 months ago
- FermiKit small variant calls for public SGDP samples☆17Updated 9 years ago
- v2.x of the microassembly based somatic variant caller☆23Updated 4 months ago
- Haplotype phaser for next-generation sequencing data☆13Updated 3 years ago
- Ximmer is a system for CNV calling on exome and targeted genomic sequencing☆19Updated last month
- Graphite - Graph-based variant adjudication☆28Updated 4 years ago
- 10x Genomics Reads Simulator☆46Updated last year
- SV analysis of the long-read sequencing data of the 1019 samples of the 1KG-ONT panel☆38Updated 7 months ago