ncbi / graf
Genetic Relationship And Fingerprinting
☆13Updated last year
Related projects: ⓘ
- ☆10Updated last year
- ☆18Updated 5 years ago
- ☆51Updated 5 years ago
- Long read to rMATS☆28Updated last year
- Code and data used to create the JASPAR UCSC Genome Browser tracks data hub☆12Updated 2 years ago
- Software used by Trinity CTAT for building CTAT Genome Libs, resource databases shared by Trinity CTAT components☆10Updated 10 months ago
- Mutation detection using GATK4 best practices and latest RNA editing filters resources. Works with both Hg38 and Hg19☆73Updated 2 months ago
- ☆23Updated 5 years ago
- Mapped QC analysis program☆41Updated 6 years ago
- An interactive learning resource for next-generation sequencing (NGS) techniques☆26Updated 5 years ago
- R tools to interact with hap.py output☆15Updated 5 years ago
- ☆12Updated 4 years ago
- rnasplice is a bioinformatics pipeline for RNA-seq alternative splicing analysis☆41Updated 3 weeks ago
- TREDPARSE: HLI Short Tandem Repeat (STR) caller☆24Updated 4 years ago
- Portable WDL workflows for IDseq production pipelines☆31Updated 2 years ago
- Workflows for processing RNA data for germline short variant discovery with GATK (v3+v4) and related tools☆49Updated 4 years ago
- A Teaching Engine for Genomics☆11Updated 3 years ago
- Flexible Bayesian inference of mutational signatures☆33Updated last year
- ☆34Updated last year
- RNA-Seq Mutation Detection☆28Updated 3 years ago
- Notes on SNP-related tools and genome variation analysis☆25Updated 2 months ago
- CADD-SV – a framework to score the effect of structural variants☆14Updated last week
- mity: A highly sensitive mitochondrial variant analysis pipeline for whole genome sequencing data☆36Updated 3 months ago
- SV clustering☆26Updated 3 years ago
- Interactive eQTL visualizations☆13Updated last year
- A simple script to create a customizable html file from an AnnotSV output.☆18Updated 4 months ago
- Run Picard on BAM files and collate 90 metrics into one file.☆39Updated 6 years ago
- Bioinformatic Analysis pipeLine for SomAtic Mutations In Cancer☆44Updated this week
- R API for browsing, analyzing, and manipulating reference-aligned genome graphs in a GenomicRanges framework☆38Updated 3 weeks ago
- A snakemake pipeline for SV analysis from nanopore genome sequencing☆51Updated 4 years ago