ExpressionAnalysis / CNV_RadarLinks
CNV Rapid Aberration Detection And Reporting
☆12Updated 4 years ago
Alternatives and similar repositories for CNV_Radar
Users that are interested in CNV_Radar are comparing it to the libraries listed below
Sorting:
- curPrimers is a tool for trimming primer sequences from amplicon based NGS reads☆16Updated last month
- A webtool for the clinical interpretation of CNVs in rare disease patients☆12Updated 3 years ago
- novoBreak: local assembly for breakpoint detection in cancer genomes☆26Updated 7 years ago
- A tool for sample swap identification in high throughput sequencing studies☆10Updated 3 months ago
- a Shiny/R application to view and annotate copy number variations☆28Updated 2 years ago
- ☆24Updated 10 months ago
- Python scripts for matching output of Pacific Biosciences IsoSeq RNA-seq pipeline to an annotation file.☆23Updated 9 years ago
- All-FIT - Allele-Frequency-based Imputation of Tumor Purity☆17Updated 5 years ago
- Abismal is a mapper of FASTQ bisulfite-converted short reads (between 50 and 1000 bases) to a FASTA reference genome.☆18Updated last week
- A set of tools to annotate VCF files with expression and readcount data☆29Updated 3 months ago
- Long read to rMATS☆31Updated 2 years ago
- SiNVICT: Ultra-Sensitive Detection of Single Nucleotide Variants and Indels in Circulating Tumour DNA☆27Updated 4 years ago
- Combined mutation recurrence and functional impact to identify coding and non-coding cancer drivers☆15Updated 6 years ago
- Identifying differentially methylated regions from MethylC-seq (bisulfite-sequencing) data☆28Updated 2 years ago
- Structural variant VCF annotation, duplicate removal and comparison☆33Updated 4 months ago
- Toolkit for the design and analysis of amplicon sequencing experiments utilizing unique molecular identifiers (UMIs)☆41Updated last year
- POSTRE: Prediction Of STRuctural variant Effects☆26Updated 4 months ago
- Structural Variation and fusion detection using targeted sequencing data from circulating cell free DNA☆28Updated last year
- Structural Variation breakpoint discovery via adaptive learning☆15Updated last year
- Somatic point mutation caller☆17Updated 8 years ago
- alternative splicing analysis pipeline☆19Updated 4 years ago
- ☆15Updated 2 years ago
- VisCap is an open flexible, software program targeted to clinical laboratories for inference and visualization of germline copy number va…☆22Updated 5 years ago
- cnv-seq with custom bugfix☆10Updated 12 years ago
- A transposition caller.☆10Updated last year
- Detection of Circular RNA and Fusions from RNA-Seq☆32Updated 6 years ago
- Automated human exome/genome variants detection from FASTQ files☆22Updated 3 years ago
- SQUID detects both fusion-gene and non-fusion-gene structural variations from RNA-seq data☆42Updated 3 years ago
- Simplify snpEff annotations for interesting cases☆22Updated 6 years ago
- A new tool to infer sex from massively parallel sequencing data.☆17Updated last month