bioforensics / MicroHapDBLinks
Portable database of microhaplotype marker and allele frequency data
☆10Updated last week
Alternatives and similar repositories for MicroHapDB
Users that are interested in MicroHapDB are comparing it to the libraries listed below
Sorting:
- 180+ Java applications for analyzing next generation sequencing data from ChIPSeq, RNASeq, BisSeq, DNASeq, variant annotation/ filtering,…☆18Updated last month
- CNV Rapid Aberration Detection And Reporting☆12Updated 4 years ago
- An efficient Variant-Caller to highlight low allele-frequency tumor mutations in a clinical practice☆11Updated 2 years ago
- IMSindel: An accurate intermediate-size indel detection tool incorporating de novo assembly and gapped global-local alignment with split …☆16Updated last year
- Multi-nucleotide variants (MNVs) in gnomAD 2.1☆12Updated 3 years ago
- Automatically design multiplex PCR primer pairs for diverse templates☆29Updated last year
- Method for Identifying Novel Transcripts and Isoforms using Equivalence classes, in cancer and rare disease.☆35Updated last year
- Calib clusters barcode tagged paired-end reads based on their barcode and sequence similarity.☆39Updated 2 years ago
- ☆14Updated 7 years ago
- Detection of Circular RNA and Fusions from RNA-Seq☆32Updated 6 years ago
- Hybridization probe design for targeted genomic sequencing of diverse and hypervariable viral taxa☆25Updated 2 years ago
- Structural variant VCF annotation, duplicate removal and comparison☆33Updated 5 months ago
- Prepare Sailfish and Salmon output for downstream analysis☆42Updated 6 years ago
- A set of tools to annotate VCF files with expression and readcount data☆29Updated 5 months ago
- Clin-mNGS: Automated pipeline for pathogen detection from clinical metagenomic data☆18Updated 4 years ago
- Structural Variation and fusion detection using targeted sequencing data from circulating cell free DNA☆29Updated last year
- "The who the what the huh?" is our pipeline for converting bcl files to fastq and performing QC.☆11Updated 2 years ago
- Long read to rMATS☆32Updated 2 years ago
- Viola is a flexible and powerful python package designed specifically for analysis of genomic structural variant (SV) signatures.☆26Updated last year
- ☆16Updated last month
- SiNVICT: Ultra-Sensitive Detection of Single Nucleotide Variants and Indels in Circulating Tumour DNA☆27Updated 4 years ago
- Splice junction analysis and filtering from BAM files☆40Updated 3 years ago
- Full-spectrum copy number variation detection by high-throughput DNA sequencing☆38Updated 3 years ago
- a Shiny/R application to view and annotate copy number variations☆28Updated 2 years ago
- Automated human exome/genome variants detection from FASTQ files☆22Updated 3 years ago
- MetaSV: An accurate and integrative structural-variant caller for next generation sequencing☆56Updated 8 years ago
- A command line tool to compute mapping statistics from a BAM file☆24Updated 3 years ago
- for visual evaluation of read support for structural variation☆54Updated last year
- alternative splicing analysis pipeline☆19Updated 4 years ago
- POSTRE: Prediction Of STRuctural variant Effects☆27Updated 5 months ago