ddbj / human-reseqLinks
☆11Updated 3 years ago
Alternatives and similar repositories for human-reseq
Users that are interested in human-reseq are comparing it to the libraries listed below
Sorting:
- Common Workflow Language definition files for workflows introduced in DAT2☆11Updated 3 years ago
- RNAseq pipeline centered on Salmon☆27Updated 7 months ago
- Step by step tutorial for CAGE analysis☆9Updated 3 years ago
- ☆15Updated 7 years ago
- Structural variant pipeline☆17Updated 5 years ago
- Web app for automated, systematic, and integrated RNA-seq differential expression analysis☆15Updated 2 months ago
- Viola is a flexible and powerful python package designed specifically for analysis of genomic structural variant (SV) signatures.☆26Updated 11 months ago
- detection of mutations causing splicing change☆13Updated 2 years ago
- About Workflow related meetup☆14Updated 6 months ago
- FRACTAL: framework for distributed computing to trace large accurate lineages☆24Updated 2 years ago
- ☆32Updated last week
- Accumulating container resource usage with workflow metadata☆19Updated 4 years ago
- A method to identify structural variation from sequencing data in target regions☆32Updated 4 years ago
- ☆13Updated 4 months ago
- ☆14Updated 2 years ago
- Nextflow implementation of the GATK HaplotypeCaller pipeline☆13Updated 3 months ago
- Simplify snpEff annotations for interesting cases☆22Updated 6 years ago
- ☆16Updated 5 months ago
- IMSindel: An accurate intermediate-size indel detection tool incorporating de novo assembly and gapped global-local alignment with split …☆16Updated last year
- Approach to identify simple and complex structural genomic rearrangements using a randomized approach☆21Updated 6 years ago
- An insertion caller for Illumina paired-end WGS data.☆23Updated 10 months ago
- Whole Exome/Whole Genome Sequencing alignment pipeline☆28Updated 9 months ago
- 🔬 Genotyping tool for genome-edited samples using nanopore-targeted sequencing☆14Updated this week
- Location of public benchmarking; primarily final results☆18Updated 4 months ago
- Ximmer is a system for CNV calling on exome and targeted genomic sequencing☆19Updated 4 months ago
- A simple script to create a customizable html file from an AnnotSV output.☆19Updated last year
- ☆21Updated 2 months ago
- Modular Multi-scale Integrated Genome Graph Browser☆92Updated this week
- Simulator for structural variants in various types of next-generation sequencing data☆9Updated 8 years ago
- Population-wide Deletion Calling☆35Updated 2 months ago