Illumina / PlatinumGenomesLinks
The Platinum Genomes Truthset
☆89Updated 8 years ago
Alternatives and similar repositories for PlatinumGenomes
Users that are interested in PlatinumGenomes are comparing it to the libraries listed below
Sorting:
- This repository contains information about latest release from Genome in a Bottle project☆75Updated 6 years ago
- NEAT read simulation tools☆101Updated 3 years ago
- A tool for profiling long STRs from short reads☆104Updated 4 years ago
- Somatic and germline variant caller for amplicon data. Recommended caller for tumor-only workflows.☆99Updated 3 years ago
- ABRA2☆95Updated 3 years ago
- ☆82Updated 7 years ago
- Runs a combination of tools to generate structural variant calls on whole-genome sequencing data☆103Updated 5 years ago
- A suite of tools for detecting expansions of short tandem repeats☆83Updated 2 years ago
- phasing and Allele Specific Expression from RNA-seq☆117Updated last year
- BAM Statistics, Feature Counting and Annotation☆152Updated last month
- ☆122Updated 5 months ago
- Read visualizer for structural variants☆84Updated 7 years ago
- 10x Genomics Linked-Read Diploid De Novo Assembler☆65Updated 7 years ago
- Script to automatically create and run IGV snapshot batchscripts☆143Updated 2 years ago
- ExomeDepth R package for the detection of copy number variants in exomes and gene panels using high throughput DNA sequencing data.☆76Updated 6 months ago
- Visualization and annotation of CNVs from population-scale whole-genome sequencing data☆72Updated 8 years ago
- don't get DUP'ed or DEL'ed by your putative SVs.☆107Updated 5 years ago
- Whole Genome Simulator for Next-Generation Sequencing☆102Updated last week
- A copy number caller for SMN1 and SMN2 to enable SMA diagnosis and carrier screening with WGS☆50Updated 2 years ago
- This WDL pipeline implements data pre-processing and initial variant calling according to the GATK Best Practices for germline SNP and In…☆55Updated 5 years ago
- WisecondorX — An evolved WISECONDOR☆108Updated last month
- Robust detection of clinically relevant structural and copy number variation from whole genome sequencing data☆75Updated last year
- Microassembly based somatic variant caller for NGS data☆154Updated 3 years ago
- Tools for processing and analyzing structural variants.☆156Updated 3 years ago
- Documenting usage and experience with bioinformatic tools☆40Updated 10 years ago
- A simple toolset for BED files (warning: CLI may change before bedtk becomes stable)☆142Updated 4 months ago
- fast and accurate alignment of BS-Seq reads using bwa-mem and a 3-letter genome☆157Updated 5 months ago
- Relevant papers for CNV and SV approaches☆94Updated last year
- Control-FREEC: Copy number and genotype annotation in whole genome and whole exome sequencing data☆175Updated last year
- C++ htslib/bwa-mem/fermi interface for interrogating sequence data☆138Updated 3 months ago