PF2-pasteur-fr / checkMyIndexLinks
Search for a set of compatible indexes for your sequencing experiment
☆11Updated 6 years ago
Alternatives and similar repositories for checkMyIndex
Users that are interested in checkMyIndex are comparing it to the libraries listed below
Sorting:
- Pipeline to evaluate and validate the accuracy of variant calling methods in genomic research☆35Updated this week
- A VSCode extension pack for nf-core developers.☆15Updated 6 months ago
- Bioinformatic Analysis pipeLine for SomAtic Mutations In Cancer☆49Updated this week
- Splice junction analysis and filtering from BAM files☆41Updated 3 years ago
- Mapped QC analysis program☆44Updated 7 years ago
- for visual evaluation of read support for structural variation☆54Updated last year
- A comprehensive cancer DNA/RNA analysis and reporting pipeline☆86Updated last week
- Fast sequencing data quality metrics☆27Updated last week
- Nextflow RNA-Seq Best Practice analysis pipeline, used at the SciLifeLab National Genomics Infrastructure.☆51Updated 7 years ago
- Examples showing how to configure Nextflow to run with Wave containers provisioning service☆21Updated 10 months ago
- Demultiplexing pipeline for sequencing data☆50Updated 2 weeks ago
- Params validation plugin for Nextflow pipelines☆48Updated last year
- A python parser to simplify and build the VCF (Variant Call Format).☆49Updated 10 months ago
- The Zavolab Automated RNA-seq Pipeline☆35Updated last month
- gatk4 RNA variant calling pipeline☆53Updated last week
- An efficient way to guess the library type of your RNA-Seq data.☆32Updated 2 years ago
- Variant catalogue pipeline☆25Updated 4 months ago
- GFF3sort: A Perl Script to sort gff3 files and produce suitable results for tabix tools☆51Updated 5 years ago
- UNDER DEVELOPMENT--- Analysis of long non-coding RNAs from RNA-seq datasets☆34Updated 5 months ago
- Fast FASTQ sample demultiplexing in Rust.☆64Updated 3 months ago
- Precision HLA typing from next-generation sequencing data☆71Updated last month
- Flexible and efficient parsing, interpreting and editing of sequencing reads☆44Updated 3 months ago
- BigWig and BAM utilities☆97Updated last year
- Merge fastq files split over lanes☆20Updated 7 years ago
- This repository hosts a large collection of Nextflow snippets☆57Updated 7 months ago
- ☆33Updated last week
- visual analysis of your VCF files☆36Updated 2 years ago
- Merging paired-end reads and removing adapters☆46Updated 6 months ago
- A collection of scripts to assist in the retrieval of data from the ENA Browser☆88Updated last month
- A nextflow pipeline to perform state-of-the-art genome-wide association studies.☆73Updated 5 months ago