magnusdv / quickpedLinks
An online pedigree tool for research applications. Build pedigrees interactively and store as images or text files in ped format. QuickPed also computes a variety of relatedness coefficients and offers verbal descriptions of pairwise relationships.
☆24Updated last month
Alternatives and similar repositories for quickped
Users that are interested in quickped are comparing it to the libraries listed below
Sorting:
- ☆15Updated last year
- A bioinformatics best-practice analysis pipeline for the analysis of shallow whole genome sequencing (sWGS) data for the identification o…☆13Updated last week
- A set of tools to annotate VCF files with expression and readcount data☆29Updated 3 months ago
- Phylogeny-based Contamination Detection in Mitochondrial and Whole-Genome Sequencing Studies☆18Updated 2 years ago
- ☆23Updated last month
- ☆41Updated 9 months ago
- Pipeline for structural variant image curation and analysis.☆48Updated 3 years ago
- Expanded STR algorithm for Illumina sequencing data☆23Updated 2 years ago
- CADD-SV – a framework to score the effect of structural variants☆14Updated 3 months ago
- Bamgineer: Introduction of simulated allele-specific copy number variants into exome and targeted sequence data sets☆37Updated 4 years ago
- Suite of tools for analysing off-target reads to find CNVs, homozygous regions, and shared haplotypes☆29Updated 11 months ago
- Bioinformatic Analysis pipeLine for SomAtic Mutations In Cancer☆47Updated this week
- Multi-sample genome coverage viewer to observe large, coverage-based anomalies alongside annotations and sample metadata☆57Updated 3 years ago
- Codes and Data for FFPEsig manuscript☆17Updated last year
- Callable Cancer Loci - assessment of sequencing coverage for actionable and pathogenic loci in cancer☆21Updated 4 years ago
- v2.x of the microassembly based somatic variant caller☆24Updated last week
- Viola is a flexible and powerful python package designed specifically for analysis of genomic structural variant (SV) signatures.☆26Updated 11 months ago
- a set of NGS pipelines☆24Updated this week
- Structural Variation breakpoint discovery via adaptive learning☆15Updated last year
- ☆25Updated 5 years ago
- Location of public benchmarking; primarily final results☆18Updated 4 months ago
- Pipeline for structural variation detection in cohorts☆49Updated 3 years ago
- Python package and routines for merging VCF files☆29Updated 4 years ago
- Model files for Sentieon variant callers☆16Updated last month
- Basic UPD caller☆11Updated 3 years ago
- Integrative analysis of complex structural variants☆21Updated 4 years ago
- ☆23Updated last year
- Structural variant (SV) analysis tools☆36Updated 11 months ago
- a bucket of bioinformatics scripts☆13Updated this week
- ☆18Updated 3 years ago