ht50 / FLT3_ITD_ext
FLT3-ITD script based on in-silico extension and clustering
☆14Updated 3 years ago
Alternatives and similar repositories for FLT3_ITD_ext:
Users that are interested in FLT3_ITD_ext are comparing it to the libraries listed below
- Create "haplotype maps" of variants in order to use with Picardtools Crosscheck_Files utility, which allows for robust genotyping of func…☆27Updated last year
- SMN1 copy-number and sequence variant analysis from next generation sequencing data☆22Updated last year
- CN-Learn☆29Updated 5 years ago
- ☆46Updated 5 years ago
- ClassifyCNV: a tool for clinical annotation of copy-number variants☆61Updated last year
- A standalone end-to-end data analysis pipeline for Duplex Sequencing☆20Updated last year
- ConsensusCruncher is a tool that suppresses errors in next-generation sequencing data by using unique molecular identifiers (UMIs) to ama…☆21Updated 2 years ago
- ☆52Updated 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…☆52Updated 4 years ago
- ☆39Updated 10 months ago
- CNV screening and annotation tool☆24Updated 8 years ago
- Robust detection of clinically relevant structural and copy number variation from whole genome sequencing data☆67Updated 5 months ago
- Bioinformatic Analysis pipeLine for SomAtic Mutations In Cancer☆45Updated this week
- SiNVICT: Ultra-Sensitive Detection of Single Nucleotide Variants and Indels in Circulating Tumour DNA☆27Updated 4 years ago
- TIDDIT - structural variant calling☆74Updated last month
- Concordance and contamination estimator for tumor–normal pairs☆57Updated 4 months ago
- WISECONDOR (WIthin-SamplE COpy Number aberration DetectOR): Detect fetal trisomies and smaller CNV's in a maternal plasma sample using wh…☆44Updated 10 months ago
- QDNAseq package for Bioconductor☆49Updated 7 months ago
- Somatic and germline variant caller for amplicon data. Recommended caller for tumor-only workflows.☆96Updated 2 years ago
- ☆14Updated last year
- Documenting usage and experience with bioinformatic tools☆41Updated 9 years ago
- ☆24Updated 5 years ago
- Benchmarking of CNV calling tools☆18Updated 5 years ago
- ☆40Updated last year
- Snakemake-based workflow for detecting structural variants in genomic data☆80Updated 2 weeks ago
- R Package for Non Invasive Prenatal Testing (NIPT) analysis☆41Updated 5 years ago
- Data and information about the Polaris study☆53Updated 5 years ago
- Stratification BED files from the Global Alliance for Genomics and Health (GA4GH) Benchmarking Team and the Genome in a Bottle Consortium…☆78Updated 2 years ago
- ☆23Updated 2 months ago
- Filtering and profiling of next-generational sequencing data using region-specific rules☆75Updated last year