drmaize / ThermoAlign
ThermoAlign: software for automated primer design
☆25Updated 6 years ago
Alternatives and similar repositories for ThermoAlign:
Users that are interested in ThermoAlign are comparing it to the libraries listed below
- Python package and routines for merging VCF files☆29Updated 3 years ago
- GEM-Mapper v3☆58Updated 4 years ago
- Pipeline for structural variation detection in cohorts☆49Updated 3 years ago
- heuristics to merge structural variant calls in VCF format.☆35Updated 8 years ago
- Seeking information like heteroplasmy, structure variants, etc. on Mitochondrial genome from next generation sequencing☆40Updated 6 years ago
- Multi-sample genome coverage viewer to observe large, coverage-based anomalies alongside annotations and sample metadata☆56Updated 2 years ago
- Adapters for trimming☆30Updated 5 years ago
- Toolkit for the design and analysis of amplicon sequencing experiments utilizing unique molecular identifiers (UMIs)☆41Updated 8 months ago
- Structural variant merging tool☆49Updated 4 months ago
- RetroSeq is a bioinformatics tool that searches for mobile element insertions from aligned reads in a BAM file and a library of reference…☆65Updated 2 years ago
- MetaSV: An accurate and integrative structural-variant caller for next generation sequencing☆55Updated 7 years ago
- for visual evaluation of read support for structural variation☆51Updated 7 months ago
- ☆39Updated 4 months ago
- ☆39Updated 8 months ago
- FLT3 ITD detection (ITDseek) and simulation (ITDsim)☆14Updated 5 years ago
- Preprocessing tools for unique molecular index (UMI) sequencing reads☆31Updated last year
- Master of Pores 2☆23Updated last month
- for detecting internal tandem duplication from genome sequence data.☆11Updated 5 years ago
- QC3, a quality control tool designed for DNA sequencing data for raw data, alignment, and variant calling.☆31Updated 8 years ago
- ☆79Updated 8 months ago
- new repo☆27Updated 3 years ago
- catalog for long-read sequencing tools☆32Updated last year
- Tools for processing and analyzing structural variants.☆32Updated 9 years ago
- Digenome-toolkit ver2.☆16Updated 3 years ago
- UCSC Nanopore☆43Updated 5 years ago
- EM based transcript abundance from nanopore reads mapped to a transcriptome with minimap2☆57Updated 3 months ago
- Full-spectrum copy number variation detection by high-throughput DNA sequencing☆37Updated 3 years ago
- A collection of command line tools for working with sequencing data☆51Updated this week
- Genotype and phase short tandem repeats using Illumina whole-genome sequencing data☆28Updated 3 years ago
- Filtering and profiling of next-generational sequencing data using region-specific rules☆74Updated last year