ncbi / grafLinks
Genetic Relationship And Fingerprinting
☆15Updated 2 years ago
Alternatives and similar repositories for graf
Users that are interested in graf are comparing it to the libraries listed below
Sorting:
- Bioinformatic Analysis pipeLine for SomAtic Mutations In Cancer☆49Updated this week
- Method for detecting STR expansions from short-read sequencing data☆63Updated 3 years ago
- A Framework to call Structural Variants from NGS based datasets☆22Updated 7 years ago
- A set of tools to annotate VCF files with expression and readcount data☆29Updated 6 months ago
- HTML5 pedigree/haplotype explorer, featuring a rich selection of comparison tools.☆10Updated 4 years ago
- for visual evaluation of read support for structural variation☆54Updated last year
- Thousand Variant Callers Project Repository☆73Updated 5 years ago
- Preprocessing tools for unique molecular index (UMI) sequencing reads☆31Updated 2 years ago
- CADD-SV – a framework to score the effect of structural variants☆15Updated 5 months ago
- Simplify snpEff annotations for interesting cases☆22Updated 6 years ago
- CLAMMS is a scalable tool for detecting common and rare copy number variants from whole-exome sequencing data.☆29Updated 4 years ago
- Genomic VCF to tab-separated values☆47Updated 2 years ago
- ☆24Updated 6 years ago
- Seeking information like heteroplasmy, structure variants, etc. on Mitochondrial genome from next generation sequencing☆41Updated 6 years ago
- Opossum is a tool to pre-process RNA-seq reads prior to variant calling.☆28Updated 7 years ago
- mity: A highly sensitive mitochondrial variant analysis pipeline for whole genome sequencing data☆37Updated this week
- Automated next generation DNA sequencing analysis pipeline suited for clinical tests, with >99.9% sensitivity to Sanger sequencing at rea…☆26Updated 5 years ago
- Generic human DNA variant annotation pipeline☆58Updated last year
- Create "haplotype maps" of variants in order to use with Picardtools Crosscheck_Files utility, which allows for robust genotyping of func…☆28Updated last year
- a set of NGS pipelines☆24Updated 2 weeks ago
- Support code for NGS copy number algorithms. Takes a file of locations and a [cr|b]am file and generates a count of coverage of each alle…☆45Updated 3 years ago
- Structural Variant Prediction Viewer☆35Updated 8 years ago
- Comprehensive benchmark of structural variant callers☆46Updated 4 years ago
- Remove primer sequence from BAM alignments by soft-clipping☆31Updated 5 years ago
- VCF-Miner: A graphical user interface for sorting, filtering and querying annotated VCF Files☆37Updated 5 years ago
- Filtering and profiling of next-generational sequencing data using region-specific rules☆25Updated 9 years ago
- ☆44Updated 11 months ago
- Ancestry and Kinship Tools☆70Updated 2 years ago
- Script to convert GTC/BPM files to VCF☆47Updated last year
- Structural Variation and fusion detection using targeted sequencing data from circulating cell free DNA☆29Updated last year