ncbi / graf
Genetic Relationship And Fingerprinting
☆14Updated 2 years ago
Alternatives and similar repositories for graf:
Users that are interested in graf are comparing it to the libraries listed below
- Long read to rMATS☆31Updated last year
- ☆51Updated 5 years ago
- TREDPARSE: HLI Short Tandem Repeat (STR) caller☆25Updated 4 years ago
- ☆11Updated last year
- ☆18Updated 6 years ago
- A set of tools to annotate VCF files with expression and readcount data☆29Updated 3 weeks ago
- Software for detecting transposable element insertions from next-generation sequencing data☆14Updated 4 years ago
- SQUID detects both fusion-gene and non-fusion-gene structural variations from RNA-seq data☆42Updated 2 years ago
- mity: A highly sensitive mitochondrial variant analysis pipeline for whole genome sequencing data☆36Updated last month
- Single Cell Caller (SCcaller) - Identify single nucleotide variations (SNVs) from single cell sequencing data☆34Updated 4 months ago
- Genomes on the Cloud, Mapping & Variant Calling Pipelines☆34Updated 8 years ago
- A tool to plot significant regions of GWAS☆29Updated 2 years ago
- ☆35Updated 3 years ago
- WDL workflow for population variant calling using htsget, DeepVariant, and GLnexus☆10Updated 6 years ago
- Create regional association plots from GWAS or meta-analysis☆61Updated 5 years ago
- Bioinformatic Analysis pipeLine for SomAtic Mutations In Cancer☆45Updated this week
- Method for Identifying Novel Transcripts and Isoforms using Equivalence classes, in cancer and rare disease.☆35Updated 8 months ago
- ☆13Updated last year
- A utility for merging and genotyping Illumina-style GVCFs.☆33Updated 6 years ago
- ☆23Updated 5 years ago
- BreakSeq2: Ultrafast and accurate nucleotide-resolution analysis of structural variants☆24Updated 9 years ago
- ☆21Updated 10 months ago
- SMN1 copy-number and sequence variant analysis from next generation sequencing data☆22Updated last year
- SV clustering☆28Updated 3 years ago
- ☆23Updated 3 years ago
- Pipeline for structural variation detection in cohorts☆49Updated 3 years ago
- deepStats: a stastitical toolbox for deeptools and genomic signals☆34Updated 3 years ago
- VCF-Miner: A graphical user interface for sorting, filtering and querying annotated VCF Files☆37Updated 5 years ago
- Liftover VCF files☆17Updated 8 years ago
- CADD-SV – a framework to score the effect of structural variants☆14Updated 2 weeks ago